"Ambry Genetics"[submitter] AND "ST8SIA6"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559041	NM_001004470.3(ST8SIA6):c.1149C>A (p.His383Gln)	ST8SIA6 (H232Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322984	NM_001004470.3(ST8SIA6):c.1117C>T (p.Pro373Ser)	ST8SIA6 (P373S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322983	NM_001004470.3(ST8SIA6):c.1061C>A (p.Pro354His)	ST8SIA6 (P354H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170741	NM_001004470.3(ST8SIA6):c.1045A>C (p.Thr349Pro)	ST8SIA6 (T198P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210970	NM_001004470.3(ST8SIA6):c.1012G>A (p.Val338Met)	ST8SIA6 (V338M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323052	NM_001004470.3(ST8SIA6):c.1008A>C (p.Lys336Asn)	ST8SIA6 (K185N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333668	NM_001004470.3(ST8SIA6):c.970G>A (p.Gly324Ser)	ST8SIA6 (G173S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170747	NM_001004470.3(ST8SIA6):c.953C>T (p.Ala318Val)	ST8SIA6 (A318V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532931	NM_001004470.3(ST8SIA6):c.943G>A (p.Gly315Ser)	ST8SIA6 (G164S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546396	NM_001004470.3(ST8SIA6):c.906G>T (p.Lys302Asn)	ST8SIA6 (K151N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347797	NM_001004470.3(ST8SIA6):c.890T>A (p.Leu297Gln)	ST8SIA6 (L297Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322982	NM_001004470.3(ST8SIA6):c.703A>T (p.Ile235Leu)	ST8SIA6 (I84L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407982	NM_001004470.3(ST8SIA6):c.502A>G (p.Ile168Val)	ST8SIA6 (I168V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170746	NM_001004470.3(ST8SIA6):c.434A>G (p.Asn145Ser)	ST8SIA6 (N145S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3170745	NM_001004470.3(ST8SIA6):c.404C>T (p.Ala135Val)	ST8SIA6 (A135V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3170744	NM_001004470.3(ST8SIA6):c.302A>C (p.Asn101Thr)	ST8SIA6 (N101T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2507868	NM_001004470.3(ST8SIA6):c.224T>G (p.Leu75Arg)	ST8SIA6, ST8SIA6-AS1 (L75R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2592456	NM_001004470.3(ST8SIA6):c.212A>C (p.Asn71Thr)	ST8SIA6, ST8SIA6-AS1 (N71T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3170743	NM_001004470.3(ST8SIA6):c.196A>T (p.Asn66Tyr)	ST8SIA6 (N66Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance