DBN1[gene] and "single gene"[properties] - ClinVar

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3080186	NM_001363541.2(DBN1):c.1996G>C (p.Val666Leu)	DBN1 (V666L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080185	NM_001363541.2(DBN1):c.1991C>T (p.Pro664Leu)	DBN1 (P601L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257938	NM_001363541.2(DBN1):c.1958C>T (p.Ala653Val)	DBN1 (A652V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 711935	NM_001363541.2(DBN1):c.1914+4C>T	DBN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2374190	NM_001363541.2(DBN1):c.1718G>T (p.Cys573Phe)	DBN1 (C529F +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622376	NM_001363541.2(DBN1):c.1694C>T (p.Pro565Leu)	DBN1 (P521L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 765144	NM_001363541.2(DBN1):c.1688C>T (p.Pro563Leu)	DBN1 (P562L +6 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2212409	NM_001363541.2(DBN1):c.1648G>A (p.Val550Ile)	DBN1 (V506I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080184	NM_001363541.2(DBN1):c.1637C>T (p.Ser546Leu)	DBN1 (S232L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386092	NM_001363541.2(DBN1):c.1571T>C (p.Leu524Pro)	DBN1 (L461P +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080182	NM_001363541.2(DBN1):c.1540G>A (p.Val514Ile)	DBN1 (V200I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080181	NM_001363541.2(DBN1):c.1465G>A (p.Ala489Thr)	DBN1 (A426T +6 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3080180	NM_001363541.2(DBN1):c.1453G>A (p.Ala485Thr)	DBN1 (A439T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617473	NM_001363541.2(DBN1):c.1444G>A (p.Val482Met)	DBN1 (V168M +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080179	NM_001363541.2(DBN1):c.1429G>A (p.Val477Ile)	DBN1 (V433I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080178	NM_001363541.2(DBN1):c.1388C>T (p.Pro463Leu)	DBN1 (P400L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080177	NM_001363541.2(DBN1):c.1297G>A (p.Glu433Lys)	DBN1 (E387K +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080175	NM_001363541.2(DBN1):c.1244C>A (p.Pro415Gln)	DBN1 (P414Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238332	NM_001363541.2(DBN1):c.1207G>C (p.Asp403His)	DBN1 (D357H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260600	NM_001363541.2(DBN1):c.1199G>A (p.Arg400Gln)	DBN1 (R337Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080174	NM_001363541.2(DBN1):c.1177C>G (p.Pro393Ala)	DBN1 (P347A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782464	NM_001363541.2(DBN1):c.1152G>A (p.Pro384=)	DBN1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3080173	NM_001363541.2(DBN1):c.1147A>C (p.Ser383Arg)	DBN1 (S320R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242414	NM_001363541.2(DBN1):c.1144C>T (p.Arg382Trp)	DBN1 (R319W +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768052	NM_001363541.2(DBN1):c.1134C>T (p.Pro378=)	DBN1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3080189	NM_001363541.2(DBN1):c.1114C>T (p.Arg372Trp)	DBN1 (R374W +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364137	NM_001363541.2(DBN1):c.928G>T (p.Val310Leu)	DBN1 (V247L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080188	NM_001363541.2(DBN1):c.927T>A (p.Asp309Glu)	DBN1 (D246E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363326	NM_001363541.2(DBN1):c.807G>A (p.Met269Ile)	DBN1 (M206I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460441	NM_001363541.2(DBN1):c.766A>G (p.Ile256Val)	DBN1 (I255V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599851	NM_001363541.2(DBN1):c.731C>T (p.Ala244Val)	DBN1 (A181V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531957	NM_001363541.2(DBN1):c.703C>A (p.His235Asn)	DBN1 (H235N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656122	NM_001363541.2(DBN1):c.687G>A (p.Glu229=)	DBN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774638	NM_001363541.2(DBN1):c.677G>A (p.Arg226Gln)	DBN1 (R225Q +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2395315	NM_001363541.2(DBN1):c.536A>G (p.Gln179Arg)	DBN1 (Q179R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482500	NM_001363541.2(DBN1):c.521G>A (p.Arg174Gln)	DBN1 (R111Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311048	NM_001363541.2(DBN1):c.475G>A (p.Val159Met)	DBN1 (V158M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377773	NM_001363541.2(DBN1):c.446G>A (p.Arg149Gln)	DBN1 (R151Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 720468	NM_001363541.2(DBN1):c.399C>T (p.Leu133=)	DBN1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2520181	NM_001363541.2(DBN1):c.377C>T (p.Ala126Val)	DBN1 (A126V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600573	NM_001363541.2(DBN1):c.337G>A (p.Asp113Asn)	DBN1 (D115N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549865	NM_001363541.2(DBN1):c.241G>A (p.Val81Met)	DBN1 (V80M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211426	NM_001363541.2(DBN1):c.163T>G (p.Ser55Ala)	DBN1 (S54A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 786533	NM_001363541.2(DBN1):c.143-5C>T	DBN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3080183	NM_001363541.2(DBN1):c.136T>A (p.Ser46Thr)	DBN1 (S48T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 782465	NM_001363541.2(DBN1):c.117T>C (p.Asp39=)	DBN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2270514	NM_001363541.2(DBN1):c.110G>A (p.Gly37Asp)	DBN1 (G37D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080176	NM_001363541.2(DBN1):c.108T>A (p.Asp36Glu)	DBN1 (D38E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080187	NM_001363541.2(DBN1):c.79G>A (p.Ala27Thr)	DBN1 (A27T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 49