RAD51D[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 986729	NM_002878.4(RAD51D):c.738+402_*1465del	RAD51D, RAD51L3-RFFL	Deletion (splice acceptor variant +1 more)	Malignant tumor of breast	GPathogenic
Select item 417528	NC_000017.11:g.(?_35099792)_(35103544_?)del	RAD51D, RAD51L3-RFFL	Deletion	Breast-ovarian cancer, familial, susceptibility to, 4	GPathogenic
Select item 239402	NM_002878.3(RAD51D):c.739-?_*1161del	RAD51D, RAD51L3-RFFL	Deletion	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely pathogenic
Select item 322611	NM_002878.4(RAD51D):c.*871CAGA[1]	RAD51D, RAD51L3-RFFL	Microsatellite (3 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility	GUncertain significance
Select item 1713232	NM_002878.4(RAD51D):c.896_*505del597insT (p.Ser299fs)	RAD51D, RAD51L3-RFFL (S187fs +2 more)	Indel (frameshift variant +3 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely pathogenic
Select item 1516502	NM_002878.4(RAD51D):c.896_*505del597 (p.Ser299_Ter329delinsXaa)	RAD51D, RAD51L3-RFFL	Deletion (stop lost +3 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely pathogenic
Select item 322615	NM_002878.4(RAD51D):c.*431CT[1]	RAD51D, RAD51L3-RFFL	Microsatellite (3 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility	GUncertain significance
Select item 1276573	NM_002878.4(RAD51D):c.*130A>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 2576265	NM_002878.4(RAD51D):c.*49C>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 926967	NM_002878.4(RAD51D):c.*16G>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 421911	NM_002878.4(RAD51D):c.*9GTT[1]	RAD51D, RAD51L3-RFFL	Microsatellite (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 920223	NM_002878.4(RAD51D):c.*11T>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 665631	NC_000017.10:g.(?_33427962)_(33446642_?)dup	RAD51D, RAD51L3-RFFL	Duplication	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 663404	NC_000017.11:g.(?_35100943)_(35103554_?)del	RAD51D, RAD51L3-RFFL	Deletion	Breast-ovarian cancer, familial, susceptibility to, 4	GPathogenic
Select item 655235	NC_000017.11:g.(?_35100943)_(35101046_?)del	RAD51D, RAD51L3-RFFL	Deletion	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely pathogenic
Select item 630038	NM_002878.4(RAD51D):c.*10T>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 378464	NM_002878.4(RAD51D):c.*7C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 584229	NC_000017.10:g.(?_33427966)_(33446638_?)dup	RAD51D, RAD51L3-RFFL	Duplication	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 472581	NC_000017.11:g.(?_35100947)_(35101042_?)del	RAD51D, RAD51L3-RFFL	Deletion	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely pathogenic
Select item 1171226	NM_002878.4(RAD51D):c.*4G>C	RAD51L3-RFFL, RAD51D	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 231210	NM_002878.4(RAD51D):c.*4G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1177656	NM_002878.4(RAD51D):c.906_*1del (p.Thr303fs)	RAD51D, RAD51L3-RFFL (T191fs +2 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 2749860	NM_002878.4(RAD51D):c.987A>C (p.Ter329Cys)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (stop lost +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 959118	NM_002878.4(RAD51D):c.987A>G (p.Ter329Trp)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (stop lost +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 823523	NM_002878.4(RAD51D):c.986G>T (p.Ter329Leu)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (stop lost +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 2999752	NM_002878.4(RAD51D):c.985T>C (p.Ter329Arg)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (stop lost +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 823505	NM_002878.4(RAD51D):c.984A>G (p.Thr328=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 141343	NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile)	RAD51D, RAD51L3-RFFL (T328I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 1407757	NM_002878.4(RAD51D):c.982A>G (p.Thr328Ala)	RAD51D, RAD51L3-RFFL (T328A +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 947018	NM_002878.4(RAD51D):c.982A>T (p.Thr328Ser)	RAD51D, RAD51L3-RFFL (T216S +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GConflicting classifications of pathogenicity
Select item 2847354	NM_002878.4(RAD51D):c.981G>A (p.Gln327=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely benign
Select item 939479	NM_002878.4(RAD51D):c.980A>T (p.Gln327Leu)	RAD51D, RAD51L3-RFFL (Q347L +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 187753	NM_002878.4(RAD51D):c.979C>T (p.Gln327Ter)	RAD51D, RAD51L3-RFFL (Q327* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided +2 more	GUncertain significance
Select item 472633	NM_002878.4(RAD51D):c.977A>C (p.Asp326Ala)	RAD51D, RAD51L3-RFFL (D326A +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1801650	NM_002878.4(RAD51D):c.974del (p.Gly325fs)	RAD51D, RAD51L3-RFFL (G213fs +2 more)	Deletion (frameshift variant +1 more)	Gastric cancer	GPathogenic
Select item 1380993	NM_002878.4(RAD51D):c.974G>T (p.Gly325Val)	RAD51D, RAD51L3-RFFL (G325V +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 1310728	NM_002878.4(RAD51D):c.974G>A (p.Gly325Asp)	RAD51D, RAD51L3-RFFL (G213D +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3222895	NM_002878.4(RAD51D):c.973G>T (p.Gly325Cys)	RAD51D, RAD51L3-RFFL (G213C +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 2011510	NM_002878.4(RAD51D):c.973G>C (p.Gly325Arg)	RAD51D, RAD51L3-RFFL (G325R +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 127898	NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser)	RAD51L3-RFFL, RAD51D (G325S +2 more)	Single nucleotide variant (missense variant +1 more)	RAD51D-related condition +5 more	GConflicting classifications of pathogenicity
Select item 2701348	NM_002878.4(RAD51D):c.972G>C (p.Gln324His)	RAD51D, RAD51L3-RFFL (Q324H +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 1768006	NM_002878.4(RAD51D):c.972G>A (p.Gln324=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 185169	NM_002878.4(RAD51D):c.972G>T (p.Gln324His)	RAD51D, RAD51L3-RFFL (Q324H +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1098871	NM_002878.4(RAD51D):c.971A>T (p.Gln324Leu)	RAD51D, RAD51L3-RFFL (Q212L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 837146	NM_002878.4(RAD51D):c.971A>G (p.Gln324Arg)	RAD51D, RAD51L3-RFFL (Q212R +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 2753664	NM_002878.4(RAD51D):c.970C>A (p.Gln324Lys)	RAD51D, RAD51L3-RFFL (Q212K +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 2709440	NM_002878.4(RAD51D):c.970C>T (p.Gln324Ter)	RAD51D, RAD51L3-RFFL (Q212* +2 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 1466890	NM_002878.4(RAD51D):c.969_970insGA (p.Gln324fs)	RAD51L3-RFFL, RAD51D (Q212fs +2 more)	Insertion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 927648	NM_002878.4(RAD51D):c.969A>G (p.Leu323=)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 2563038	NM_002878.4(RAD51D):c.968T>G (p.Leu323Ter)	RAD51D, RAD51L3-RFFL (L323* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1767798	NM_002878.4(RAD51D):c.968T>C (p.Leu323Ser)	RAD51D, RAD51L3-RFFL (L343S +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1391074	NM_002878.4(RAD51D):c.968T>A (p.Leu323Ter)	RAD51D, RAD51L3-RFFL (L323* +2 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 823400	NM_002878.4(RAD51D):c.968delinsAAG (p.Leu323Ter)	RAD51D, RAD51L3-RFFL (L211* +2 more)	Indel (nonsense +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1416150	NM_002878.4(RAD51D):c.967T>G (p.Leu323Val)	RAD51D, RAD51L3-RFFL (L211V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 186888	NM_002878.4(RAD51D):c.966A>G (p.Thr322=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GLikely benign
Select item 490150	NM_002878.4(RAD51D):c.963dup (p.Thr322fs)	RAD51D, RAD51L3-RFFL (T322fs +2 more)	Duplication (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 849774	NM_002878.4(RAD51D):c.963del (p.Thr322fs)	RAD51D, RAD51L3-RFFL (T342fs +2 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 1767570	NM_002878.4(RAD51D):c.960T>C (p.Ser320=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 472632	NM_002878.4(RAD51D):c.955_959dup (p.Ala321fs)	RAD51D, RAD51L3-RFFL (A209fs +2 more)	Microsatellite (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2563029	NM_002878.4(RAD51D):c.959G>A (p.Ser320Asn)	RAD51D, RAD51L3-RFFL (S208N +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 844601	NM_002878.4(RAD51D):c.959G>C (p.Ser320Thr)	RAD51D, RAD51L3-RFFL (S208T +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 480539	NM_002878.4(RAD51D):c.959G>T (p.Ser320Ile)	RAD51D, RAD51L3-RFFL (S320I +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2866042	NM_002878.4(RAD51D):c.957G>C (p.Gln319His)	RAD51D, RAD51L3-RFFL (Q339H +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 1018277	NM_002878.4(RAD51D):c.957G>T (p.Gln319His)	RAD51D, RAD51L3-RFFL (Q207H +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 184398	NM_002878.4(RAD51D):c.957G>A (p.Gln319=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	not provided +4 more	GLikely benign
Select item 193645	NM_002878.4(RAD51D):c.955C>T (p.Gln319Ter)	RAD51D, RAD51L3-RFFL (Q319* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 229668	NM_002878.4(RAD51D):c.954G>A (p.Glu318=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely benign
Select item 823321	NM_002878.4(RAD51D):c.953A>G (p.Glu318Gly)	RAD51D, RAD51L3-RFFL (E338G +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 230736	NM_002878.4(RAD51D):c.952G>A (p.Glu318Lys)	RAD51D, RAD51L3-RFFL (E318K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 1767212	NM_002878.4(RAD51D):c.950C>T (p.Ser317Leu)	RAD51D, RAD51L3-RFFL (S337L +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1767113	NM_002878.4(RAD51D):c.948C>T (p.Thr316=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1576230	NM_002878.4(RAD51D):c.948C>G (p.Thr316=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely benign
Select item 490149	NM_002878.4(RAD51D):c.946dup (p.Thr316fs)	RAD51D, RAD51L3-RFFL (T204fs +2 more)	Duplication (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1051132	NM_002878.4(RAD51D):c.945del (p.Thr316fs)	RAD51D, RAD51L3-RFFL (T204fs +2 more)	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 231010	NM_002878.4(RAD51D):c.945G>A (p.Gly315=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely benign
Select item 231621	NM_002878.4(RAD51D):c.944G>T (p.Gly315Val)	RAD51D, RAD51L3-RFFL (G315V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 186687	NM_002878.4(RAD51D):c.944G>A (p.Gly315Glu)	RAD51L3-RFFL, RAD51D (G315E +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 185649	NM_002878.4(RAD51D):c.943G>C (p.Gly315Arg)	RAD51D, RAD51L3-RFFL (G315R +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2114668	NM_002878.4(RAD51D):c.942G>C (p.Trp314Cys)	RAD51D, RAD51L3-RFFL (W202C +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 2448044	NM_002878.4(RAD51D):c.941G>C (p.Trp314Ser)	RAD51L3-RFFL, RAD51D (W314S +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1801549	NM_002878.4(RAD51D):c.941G>A (p.Trp314Ter)	RAD51D, RAD51L3-RFFL (W202* +2 more)	Single nucleotide variant (nonsense +1 more)	Gastric cancer	GPathogenic
Select item 141612	NM_002878.4(RAD51D):c.940T>C (p.Trp314Arg)	RAD51D, RAD51L3-RFFL (W314R +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1140247	NM_002878.4(RAD51D):c.939C>G (p.Thr313=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 630700	NM_002878.4(RAD51D):c.939C>A (p.Thr313=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely benign
Select item 2809575	NM_002878.4(RAD51D):c.938C>T (p.Thr313Ile)	RAD51D, RAD51L3-RFFL (T333I +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 1017562	NM_002878.4(RAD51D):c.938C>G (p.Thr313Ser)	RAD51D, RAD51L3-RFFL (T201S +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 823206	NM_002878.4(RAD51D):c.938C>A (p.Thr313Asn)	RAD51D, RAD51L3-RFFL (T201N +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1766711	NM_002878.4(RAD51D):c.936G>C (p.Gly312=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1171622	NM_002878.4(RAD51D):c.935G>A (p.Gly312Glu)	RAD51D, RAD51L3-RFFL (G200E +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 922195	NM_002878.4(RAD51D):c.935G>C (p.Gly312Ala)	RAD51D, RAD51L3-RFFL (G312A +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 823188	NM_002878.4(RAD51D):c.935G>T (p.Gly312Val)	RAD51D, RAD51L3-RFFL (G200V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2678188	NM_002878.4(RAD51D):c.934G>T (p.Gly312Trp)	RAD51D, RAD51L3-RFFL (G200W +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 1645830	NM_002878.4(RAD51D):c.933T>C (p.Ile311=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 322623	NM_002878.4(RAD51D):c.933T>G (p.Ile311Met)	RAD51D, RAD51L3-RFFL (I311M +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 539849	NM_002878.4(RAD51D):c.924_932del (p.Met308_Asp310del)	RAD51D, RAD51L3-RFFL	Deletion (inframe_deletion +1 more)	not provided +2 more	GUncertain significance
Select item 127897	NM_002878.4(RAD51D):c.932T>C (p.Ile311Thr)	RAD51D, RAD51L3-RFFL (I311T +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 127896	NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn)	RAD51D, RAD51L3-RFFL (I311N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 2448043	NM_002878.4(RAD51D):c.931A>T (p.Ile311Phe)	RAD51D, RAD51L3-RFFL (I199F +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 960865	NM_002878.4(RAD51D):c.931A>C (p.Ile311Leu)	RAD51D, RAD51L3-RFFL (I311L +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 584560	NM_002878.4(RAD51D):c.931A>G (p.Ile311Val)	RAD51D, RAD51L3-RFFL (I311V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity

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