Related gene-specific medical variations for Gene (Select 1856) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274120	NM_004422.3(DVL2):c.689C>T (p.Ser230Phe)	DVL2, LOC126862480 (S230F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274118	NM_004422.3(DVL2):c.272C>A (p.Ser91Tyr)	DVL2, LOC126862480 (S91Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274113	NM_004422.3(DVL2):c.341C>T (p.Ala114Val)	DVL2, LOC126862480 (A114V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086399	NM_004422.3(DVL2):c.647C>T (p.Thr216Ile)	DVL2, LOC126862480 (T216I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086398	NM_004422.3(DVL2):c.622C>G (p.Leu208Val)	DVL2, LOC126862480 (L208V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086397	NM_004422.3(DVL2):c.542G>A (p.Gly181Asp)	DVL2, LOC126862480 (G181D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086396	NM_004422.3(DVL2):c.383T>C (p.Ile128Thr)	DVL2, LOC126862480 (I128T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086394	NM_004422.3(DVL2):c.301C>T (p.Pro101Ser)	DVL2, LOC126862480 (P101S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060815	NM_004422.3(DVL2):c.405C>T (p.Ser135=)	DVL2, LOC126862480	Single nucleotide variant (synonymous variant)	DVL2-related disorder	GBenign
Select item 3057425	NM_004422.3(DVL2):c.332C>T (p.Ala111Val)	DVL2, LOC126862480 (A111V)	Single nucleotide variant (missense variant)	DVL2-related disorder	GLikely benign
Select item 3056184	NM_004422.3(DVL2):c.410+10T>C	DVL2, LOC126862480	Single nucleotide variant (intron variant)	DVL2-related disorder	GBenign
Select item 3047696	NM_004422.3(DVL2):c.-4G>C	DVL2, LOC130060114	Single nucleotide variant (5 prime UTR variant)	DVL2-related disorder	GLikely benign
Select item 3046278	NM_004422.3(DVL2):c.579G>A (p.Glu193=)	DVL2, LOC126862480	Single nucleotide variant (synonymous variant)	DVL2-related disorder	GLikely benign
Select item 3038109	NM_004422.3(DVL2):c.656+8T>G	DVL2, LOC126862480	Single nucleotide variant (intron variant)	DVL2-related disorder	GLikely benign
Select item 2593353	NM_004422.3(DVL2):c.289C>T (p.Pro97Ser)	DVL2, LOC126862480 (P97S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536876	NM_004422.3(DVL2):c.636C>G (p.Asp212Glu)	DVL2, LOC126862480 (D212E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520624	NM_004422.3(DVL2):c.356C>T (p.Pro119Leu)	DVL2, LOC126862480 (P119L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492792	NM_004422.3(DVL2):c.481C>T (p.Arg161Trp)	DVL2, LOC126862480 (R161W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279789	NM_004422.3(DVL2):c.442G>C (p.Glu148Gln)	DVL2, LOC126862480 (E148Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245551	NM_004422.3(DVL2):c.374C>T (p.Thr125Ile)	DVL2, LOC126862480 (T125I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212050	NM_004422.3(DVL2):c.559C>T (p.Arg187Cys)	DVL2, LOC126862480 (R187C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 511152	NM_004422.3(DVL2):c.621C>T (p.Ser207=)	DVL2, LOC126862480	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign

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Links from Gene

Items: 22