Related gene-specific medical variations for Gene (Select 7482) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 62

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333216	NM_024494.3(WNT2B):c.962C>T (p.Ala321Val)	ST7L, WNT2B (A229V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333214	NM_024494.3(WNT2B):c.37C>T (p.Leu13Phe)	LOC129931208, WNT2B (L13F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190727	NM_024494.3(WNT2B):c.983C>T (p.Thr328Ile)	ST7L, WNT2B (T236I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190726	NM_024494.3(WNT2B):c.967C>T (p.Arg323Cys)	ST7L, WNT2B (R231C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190725	NM_024494.3(WNT2B):c.94G>C (p.Gly32Arg)	LOC122094899, WNT2B (G32R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190722	NM_024494.3(WNT2B):c.1097G>A (p.Arg366Gln)	ST7L, WNT2B (R366Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2908726	NM_024494.3(WNT2B):c.1017C>T (p.Cys339=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2908630	NM_024494.3(WNT2B):c.948T>C (p.Gly316=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2905444	NM_024494.3(WNT2B):c.1032C>T (p.Tyr344=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2888002	NM_024494.3(WNT2B):c.1173C>G (p.Thr391=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877051	NM_024494.3(WNT2B):c.9A>G (p.Arg3=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2876619	NM_024494.3(WNT2B):c.150G>A (p.Leu50=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2869382	NM_024494.3(WNT2B):c.182+15C>A	LOC122094899, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867647	NM_024494.3(WNT2B):c.102G>A (p.Arg34=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2862160	NM_024494.3(WNT2B):c.153G>T (p.Thr51=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2841916	NM_024494.3(WNT2B):c.1062G>A (p.Gln354=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2819968	NM_024494.3(WNT2B):c.12G>A (p.Pro4=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2810135	NM_024494.3(WNT2B):c.54C>G (p.Ala18=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2795858	NM_024494.3(WNT2B):c.90C>T (p.Pro30=)	WNT2B, LOC122094899	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2793117	NM_024494.3(WNT2B):c.947-18C>T	ST7L, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2776256	NM_024494.3(WNT2B):c.69T>C (p.Pro23=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2776011	NM_024494.3(WNT2B):c.12G>C (p.Pro4=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2745879	NM_024494.3(WNT2B):c.126C>G (p.Ala42=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2743128	NM_024494.3(WNT2B):c.1143C>T (p.Ala381=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2730090	NM_024494.3(WNT2B):c.969T>C (p.Arg323=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2712168	NM_024494.3(WNT2B):c.1096C>A (p.Arg366=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2710362	NM_024494.3(WNT2B):c.1158G>A (p.Glu386=)	WNT2B, ST7L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2536566	NM_024494.3(WNT2B):c.1033G>A (p.Asp345Asn)	ST7L, WNT2B (D345N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516583	NM_024494.3(WNT2B):c.79C>T (p.Pro27Ser)	LOC122094899, WNT2B (P27S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493435	NM_024494.3(WNT2B):c.994A>G (p.Thr332Ala)	ST7L, WNT2B (T240A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320366	NM_024494.3(WNT2B):c.1159T>C (p.Trp387Arg)	ST7L, WNT2B (W387R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309266	NM_024494.3(WNT2B):c.65T>C (p.Val22Ala)	LOC122094899, WNT2B (V22A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2170828	NM_024494.3(WNT2B):c.1000G>A (p.Gly334Ser)	ST7L, WNT2B (G334S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2127316	NM_024494.3(WNT2B):c.158C>G (p.Pro53Arg)	LOC122094899, WNT2B (P53R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2123833	NM_024494.3(WNT2B):c.182+8del	LOC122094899, WNT2B	Deletion (intron variant)	not provided	GLikely benign
Select item 2119068	NM_024494.3(WNT2B):c.11C>T (p.Pro4Leu)	LOC129931208, WNT2B (P4L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2116080	NM_024494.3(WNT2B):c.1172C>A (p.Thr391Asn)	ST7L, WNT2B (T299N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2100215	NM_024494.3(WNT2B):c.23A>C (p.Glu8Ala)	LOC129931208, WNT2B (E8A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2086741	NM_024494.3(WNT2B):c.47G>C (p.Arg16Pro)	LOC122094899, LOC129931208 +1 more (R16P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2065166	NM_024494.3(WNT2B):c.1142C>T (p.Ala381Val)	ST7L, WNT2B (A362V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2062623	NM_024494.3(WNT2B):c.176C>G (p.Ser59Cys)	LOC122094899, WNT2B (S59C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2055556	NM_024494.3(WNT2B):c.151A>G (p.Thr51Ala)	LOC122094899, WNT2B (T51A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2041928	NM_024494.3(WNT2B):c.1059C>G (p.Thr353=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2040803	NM_024494.3(WNT2B):c.1126G>A (p.Val376Ile)	ST7L, WNT2B (V357I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2038351	NM_024494.3(WNT2B):c.947-16C>G	ST7L, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2013692	NM_024494.3(WNT2B):c.139CTG[5] (p.Leu50_Thr51insLeu)	LOC122094899, WNT2B	Microsatellite (inframe_insertion +1 more)	not provided	GUncertain significance
Select item 1977921	NM_024494.3(WNT2B):c.73C>A (p.Pro25Thr)	LOC122094899, WNT2B (P25T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1977866	NM_024494.3(WNT2B):c.78G>A (p.Ser26=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1977262	NM_024494.3(WNT2B):c.67C>T (p.Pro23Ser)	LOC122094899, WNT2B (P23S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1974920	NM_024494.3(WNT2B):c.1052G>A (p.Arg351His)	ST7L, WNT2B (R259H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1973984	NM_024494.3(WNT2B):c.160G>A (p.Ala54Thr)	LOC122094899, WNT2B (A54T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1973531	NM_024494.3(WNT2B):c.52G>A (p.Ala18Thr)	LOC122094899, WNT2B (A18T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1973414	NM_024494.3(WNT2B):c.35A>G (p.Gln12Arg)	LOC129931208, WNT2B (Q12R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1972774	NM_024494.3(WNT2B):c.62C>G (p.Pro21Arg)	LOC122094899, WNT2B (P21R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1972665	NM_024494.3(WNT2B):c.13G>C (p.Gly5Arg)	LOC129931208, WNT2B (G5R)	Single nucleotide variant (intron variant +1 more)	not provided +1 more	GUncertain significance
Select item 1971432	NM_024494.3(WNT2B):c.947-4C>T	ST7L, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1971329	NM_024494.3(WNT2B):c.49C>T (p.Arg17Cys)	LOC122094899, LOC129931208 +1 more (R17C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1970983	NM_024494.3(WNT2B):c.82G>A (p.Ala28Thr)	LOC122094899, WNT2B (A28T)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1970963	NM_024494.3(WNT2B):c.25G>A (p.Glu9Lys)	LOC129931208, WNT2B (E9K)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1608306	NM_024494.3(WNT2B):c.1170A>G (p.Gln390=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780256	NM_024494.3(WNT2B):c.1140A>G (p.Lys380=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 767688	NM_017744.5(ST7L):c.1712G>A (p.Gly571Asp)	ST7L, WNT2B (G388D +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 62