"Ambry Genetics"[submitter] AND "VIM-AS1"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606641	NM_003380.5(VIM):c.55G>A (p.Gly19Ser)	VIM, VIM-AS1 (G19S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2303431	NM_003380.5(VIM):c.89A>G (p.Tyr30Cys)	VIM, VIM-AS1 (Y30C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2336353	NM_003380.5(VIM):c.91G>C (p.Val31Leu)	VIM, VIM-AS1 (V31L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3188560	NM_003380.5(VIM):c.209T>C (p.Leu70Pro)	LOC130003452, VIM +1 more (L70P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3188561	NM_003380.5(VIM):c.216C>G (p.Ser72Arg)	LOC130003452, VIM +1 more (S72R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2519548	NM_003380.5(VIM):c.229G>A (p.Val77Met)	LOC130003452, VIM +1 more (V77M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3188562	NM_003380.5(VIM):c.276C>G (p.Ile92Met)	VIM, VIM-AS1 (I92M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2322607	NM_003380.5(VIM):c.286T>C (p.Phe96Leu)	VIM, VIM-AS1 (F96L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance