"Ambry Genetics"[submitter] AND "ST7L"[gene] - ClinVar

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Items: 31

	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 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 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 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 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 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 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 3170712	NM_017744.5(ST7L):c.1606A>G (p.Ile536Val)	ST7L (I505V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303296	NM_017744.5(ST7L):c.1561T>C (p.Ser521Pro)	ST7L (S521P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353806	NM_017744.5(ST7L):c.1466C>T (p.Thr489Met)	ST7L (T489M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2468377	NM_017744.5(ST7L):c.1322A>G (p.Tyr441Cys)	ST7L (Y424C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170711	NM_017744.5(ST7L):c.1030G>A (p.Ala344Thr)	ST7L (A327T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327151	NM_017744.5(ST7L):c.983T>C (p.Met328Thr)	ST7L (M328T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322970	NM_017744.5(ST7L):c.953A>G (p.Asp318Gly)	ST7L (D318G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385888	NM_017744.5(ST7L):c.901A>G (p.Met301Val)	ST7L (M118V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170716	NM_017744.5(ST7L):c.872T>A (p.Val291Glu)	ST7L (V274E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170715	NM_017744.5(ST7L):c.845A>G (p.Glu282Gly)	ST7L (E265G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304642	NM_017744.5(ST7L):c.842A>G (p.His281Arg)	ST7L (H264R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270416	NM_017744.5(ST7L):c.748A>G (p.Ile250Val)	ST7L (I233V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489069	NM_017744.5(ST7L):c.637T>C (p.Trp213Arg)	ST7L (W196R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603442	NM_017744.5(ST7L):c.400G>C (p.Gly134Arg)	ST7L (G134R +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2310703	NM_017744.5(ST7L):c.387C>A (p.Ser129Arg)	ST7L (S129R +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2618814	NM_017744.5(ST7L):c.320G>C (p.Gly107Ala)	ST7L (G90A +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2523752	NM_017744.5(ST7L):c.311A>G (p.His104Arg)	ST7L (H104R +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2314091	NM_017744.5(ST7L):c.292T>C (p.Phe98Leu)	ST7L (F81L +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3170713	NM_017744.5(ST7L):c.163G>A (p.Ala55Thr)	ST7L (A55T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2622188	NM_017744.5(ST7L):c.146G>C (p.Gly49Ala)	ST7L (G49A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2458923	NM_017744.5(ST7L):c.124G>A (p.Ala42Thr)	ST7L (A42T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2469580	NM_017744.5(ST7L):c.122G>A (p.Gly41Glu)	ST7L (G41E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2401337	NM_017744.5(ST7L):c.44C>T (p.Ala15Val)	ST7L (A15V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2614574	NM_017744.5(ST7L):c.25G>C (p.Glu9Gln)	ST7L (E9Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 31