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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 25

	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 3332063	NM_003380.5(VIM):c.229G>C (p.Val77Leu)	LOC130003452, VIM +1 more (V77L)	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
Select item 3332062	NM_003380.5(VIM):c.508C>T (p.Arg170Cys)	VIM, VIM-AS1 (R170C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2399480	NM_003380.5(VIM):c.649C>A (p.Arg217Ser)	VIM (R217S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533311	NM_003380.5(VIM):c.664C>T (p.Arg222Cys)	VIM (R222C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328607	NM_003380.5(VIM):c.860C>T (p.Ala287Val)	VIM (A287V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188558	NM_003380.5(VIM):c.1046A>G (p.Glu349Gly)	VIM (E349G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362840	NM_003380.5(VIM):c.1051T>G (p.Phe351Val)	VIM (F351V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306133	NM_003380.5(VIM):c.1057G>A (p.Val353Ile)	VIM (V353I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368041	NM_003380.5(VIM):c.1080C>G (p.Asp360Glu)	VIM (D360E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541892	NM_003380.5(VIM):c.1090C>T (p.Arg364Cys)	VIM (R364C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332064	NM_003380.5(VIM):c.1142G>A (p.Arg381His)	VIM (R381H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340119	NM_003380.5(VIM):c.1195A>G (p.Thr399Ala)	VIM (T399A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317236	NM_003380.5(VIM):c.1265A>C (p.Asn422Thr)	VIM (N422T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332061	NM_003380.5(VIM):c.1312T>C (p.Ser438Pro)	VIM (S438P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188559	NM_003380.5(VIM):c.1343A>G (p.Glu448Gly)	VIM (E448G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530389	NM_003380.5(VIM):c.1360G>A (p.Val454Ile)	VIM (V454I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345133	NM_003380.5(VIM):c.1372A>G (p.Thr458Ala)	VIM (T458A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 25