"Ambry Genetics"[submitter] AND "LOC129931679"[gene] - ClinVar - NCBI

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Items: 7

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2537284	NM_001013661.1(VSIG8):c.1160C>T (p.Ser387Phe)	LOC129931679, SNHG28 +1 more (S387F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2274675	NM_001013661.1(VSIG8):c.1138G>A (p.Ala380Thr)	LOC129931679, SNHG28 +1 more (A380T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3332356	NM_001013661.1(VSIG8):c.1100G>A (p.Gly367Asp)	LOC129931679, SNHG28 +1 more (G367D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2346107	NM_001013661.1(VSIG8):c.1091C>G (p.Pro364Arg)	LOC129931679, SNHG28 +1 more (P364R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2565549	NM_001013661.1(VSIG8):c.1078T>A (p.Tyr360Asn)	LOC129931679, SNHG28 +1 more (Y360N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2355087	NM_001013661.1(VSIG8):c.1073G>T (p.Arg358Leu)	LOC129931679, SNHG28 +1 more (R358L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2465505	NM_001013661.1(VSIG8):c.1042C>T (p.Pro348Ser)	LOC129931679, SNHG28 +1 more (P348S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance