Related gene-specific medical variations for Gene (Select 26045) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3292110	NM_015564.3(LRRTM2):c.1022G>A (p.Ser341Asn)	CTNNA1, LRRTM2 (S341N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121219	NM_015564.3(LRRTM2):c.960T>G (p.Cys320Trp)	CTNNA1, LRRTM2 (C320W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121218	NM_015564.3(LRRTM2):c.437C>T (p.Ser146Leu)	CTNNA1, LRRTM2 (S146L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121217	NM_015564.3(LRRTM2):c.178G>A (p.Asp60Asn)	CTNNA1, LRRTM2 (D60N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121216	NM_015564.3(LRRTM2):c.1468A>C (p.Thr490Pro)	CTNNA1, LRRTM2 (T490P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121215	NM_015564.3(LRRTM2):c.1158C>A (p.Ser386Arg)	CTNNA1, LRRTM2 (S386R)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 2616062	NM_015564.3(LRRTM2):c.1136C>T (p.Thr379Ile)	CTNNA1, LRRTM2 (T379I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592508	NM_015564.3(LRRTM2):c.698C>T (p.Thr233Met)	CTNNA1, LRRTM2 (T233M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548191	NM_015564.3(LRRTM2):c.1214T>C (p.Val405Ala)	CTNNA1, LRRTM2 (V405A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526777	NM_015564.3(LRRTM2):c.1465C>A (p.Pro489Thr)	CTNNA1, LRRTM2 (P489T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524022	NM_015564.3(LRRTM2):c.905C>A (p.Ser302Tyr)	CTNNA1, LRRTM2 (S302Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480913	NM_015564.3(LRRTM2):c.520G>A (p.Val174Ile)	CTNNA1, LRRTM2 (V174I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371087	NM_015564.3(LRRTM2):c.1412C>T (p.Thr471Ile)	CTNNA1, LRRTM2 (T471I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341171	NM_015564.3(LRRTM2):c.950C>T (p.Ala317Val)	CTNNA1, LRRTM2 (A317V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329191	NM_015564.3(LRRTM2):c.1112C>T (p.Ala371Val)	CTNNA1, LRRTM2 (A371V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239008	NM_015564.3(LRRTM2):c.541C>T (p.Arg181Cys)	CTNNA1, LRRTM2 (R181C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211962	NM_015564.3(LRRTM2):c.254G>C (p.Ser85Thr)	CTNNA1, LRRTM2 (S85T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 223788	NM_015564.3(LRRTM2):c.4+18T>G	CTNNA1, LRRTM2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223765	NM_015564.3(LRRTM2):c.*3762A>G	CTNNA1, LRRTM2	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign