WIF1[gene] and "single gene"[properties] - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 746947	NM_007191.5(WIF1):c.1104G>A (p.Glu368=)	WIF1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3190542	NM_007191.5(WIF1):c.1085C>T (p.Ser362Leu)	WIF1 (S362L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710452	NM_007191.5(WIF1):c.1081C>A (p.Pro361Thr)	WIF1 (P361T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2603728	NM_007191.5(WIF1):c.1078A>G (p.Thr360Ala)	WIF1 (T360A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190541	NM_007191.5(WIF1):c.1040A>G (p.His347Arg)	WIF1 (H347R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712180	NM_007191.5(WIF1):c.981A>G (p.Gln327=)	WIF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3190546	NM_007191.5(WIF1):c.946G>A (p.Ala316Thr)	WIF1 (A316T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1236341	NM_007191.5(WIF1):c.930C>T (p.Cys310=)	WIF1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1266554	NM_007191.5(WIF1):c.923-78T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222654	NM_007191.5(WIF1):c.922+69A>G	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3190545	NM_007191.5(WIF1):c.921G>T (p.Lys307Asn)	WIF1 (K307N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608759	NM_007191.5(WIF1):c.908A>T (p.Asp303Val)	WIF1 (D303V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1181766	NM_007191.5(WIF1):c.827-152dup	WIF1	Duplication (intron variant)	not provided	GBenign
Select item 2620749	NM_007191.5(WIF1):c.787A>G (p.Ile263Val)	WIF1 (I263V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1278731	NM_007191.5(WIF1):c.731-109T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287191	NM_007191.5(WIF1):c.730+53T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2248208	NM_007191.5(WIF1):c.686T>C (p.Phe229Ser)	WIF1 (F229S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1280486	NM_007191.5(WIF1):c.635-163A>G	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228551	NM_007191.5(WIF1):c.634+18T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 981866	NM_007191.5(WIF1):c.608G>A (p.Gly203Glu)	WIF1 (G203E)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 2275852	NM_007191.5(WIF1):c.605A>G (p.Asp202Gly)	WIF1 (D202G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265848	NM_007191.5(WIF1):c.560G>A (p.Arg187Gln)	WIF1 (R187Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1284111	NM_007191.5(WIF1):c.538+79CA[21]	WIF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1260370	NM_007191.5(WIF1):c.538+79CA[20]	WIF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1258144	NM_007191.5(WIF1):c.538+79CA[19]	WIF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1297944	NM_007191.5(WIF1):c.538+79CA[16]	WIF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1250261	NM_007191.5(WIF1):c.538+79CA[17]	WIF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1245221	NM_007191.5(WIF1):c.538+79CA[13]	WIF1	Microsatellite (intron variant)	not provided	GBenign
Select item 2252058	NM_007191.5(WIF1):c.491T>C (p.Ile164Thr)	WIF1 (I164T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242396	NM_007191.5(WIF1):c.488C>A (p.Thr163Asn)	WIF1 (T163N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1286419	NM_007191.5(WIF1):c.459T>C (p.Asp153=)	WIF1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1283557	NM_007191.5(WIF1):c.398-76T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243665	NM_007191.5(WIF1):c.397+59T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252468	NM_007191.5(WIF1):c.289-146G>T	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 733506	NM_007191.5(WIF1):c.244G>C (p.Val82Leu)	WIF1 (V82L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1269441	NM_007191.5(WIF1):c.219A>G (p.Ala73=)	WIF1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2533270	NM_007191.5(WIF1):c.218C>A (p.Ala73Glu)	WIF1 (A73E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190543	NM_007191.5(WIF1):c.193C>T (p.Pro65Ser)	WIF1 (P65S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1289928	NM_007191.5(WIF1):c.149-202C>G	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288075	NM_007191.5(WIF1):c.149-234T>C	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1297943	NM_007191.5(WIF1):c.148+106C>T	WIF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2384356	NM_007191.5(WIF1):c.139G>T (p.Val47Leu)	WIF1 (V47L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362300	NM_007191.5(WIF1):c.82G>A (p.Ala28Thr)	WIF1 (A28T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 453256	NM_007191.5(WIF1):c.45G>A (p.Trp15Ter)	WIF1	Single nucleotide variant (nonsense)	not provided	GUncertain significance

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Items: 44