RASSF6[gene] and "single gene"[properties] - ClinVar

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

Search results

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2459418	NM_177532.5(RASSF6):c.956C>T (p.Ala319Val)	RASSF6 (A307V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151946	NM_177532.5(RASSF6):c.955G>A (p.Ala319Thr)	RASSF6 (A307T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 727256	NM_177532.5(RASSF6):c.870T>A (p.Ser290=)	RASSF6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3151958	NM_177532.5(RASSF6):c.863A>T (p.His288Leu)	RASSF6 (H254L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248657	NM_177532.5(RASSF6):c.841G>A (p.Val281Met)	RASSF6 (V281M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151957	NM_177532.5(RASSF6):c.799A>G (p.Ile267Val)	RASSF6 (I255V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592182	NM_177532.5(RASSF6):c.797G>A (p.Arg266His)	RASSF6 (R298H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362552	NM_177532.5(RASSF6):c.797G>T (p.Arg266Leu)	RASSF6 (R254L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151956	NM_177532.5(RASSF6):c.719G>A (p.Gly240Glu)	RASSF6 (G206E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312985	NM_177532.5(RASSF6):c.613G>A (p.Val205Ile)	RASSF6 (V237I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3151955	NM_177532.5(RASSF6):c.522A>T (p.Arg174Ser)	RASSF6 (R162S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495272	NM_177532.5(RASSF6):c.460A>G (p.Met154Val)	RASSF6 (M154V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323505	NM_177532.5(RASSF6):c.405C>A (p.Asn135Lys)	RASSF6 (N167K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151952	NM_177532.5(RASSF6):c.340A>G (p.Arg114Gly)	RASSF6 (R114G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536905	NM_177532.5(RASSF6):c.329G>C (p.Ser110Thr)	RASSF6 (S110T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394171	NM_177532.5(RASSF6):c.313G>C (p.Asp105His)	RASSF6 (D137H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375471	NM_177532.5(RASSF6):c.305A>T (p.Glu102Val)	RASSF6 (E90V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401220	NM_177532.5(RASSF6):c.296G>A (p.Arg99His)	RASSF6 (R87H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405200	NM_177532.5(RASSF6):c.295C>T (p.Arg99Cys)	RASSF6 (R131C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282245	NM_177532.5(RASSF6):c.277T>C (p.Ser93Pro)	RASSF6 (S93P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312986	NM_177532.5(RASSF6):c.257T>G (p.Met86Arg)	RASSF6 (M74R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211078	NM_177532.5(RASSF6):c.242C>T (p.Ser81Phe)	RASSF6 (S113F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322871	NM_177532.5(RASSF6):c.149A>G (p.Glu50Gly)	RASSF6 (E38G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151948	NM_177532.5(RASSF6):c.135A>T (p.Leu45Phe)	RASSF6 (L77F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299454	NM_177532.5(RASSF6):c.127C>T (p.His43Tyr)	RASSF6 (H43Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269272	NM_177532.5(RASSF6):c.59T>C (p.Ile20Thr)	RASSF6 (I20T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232467	NM_177532.5(RASSF6):c.57C>G (p.Phe19Leu)	RASSF6 (F19L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151947	NM_177532.5(RASSF6):c.13G>T (p.Ala5Ser)	RASSF6 (A37S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 727257	NM_177532.5(RASSF6):c.8T>C (p.Met3Thr)	RASSF6 (M3T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3312987	NM_177532.5(RASSF6):c.-11A>C	RASSF6 (K29T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2240124	NM_177532.5(RASSF6):c.-12A>G	RASSF6 (K29E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2358289	NM_177532.5(RASSF6):c.-20A>T	RASSF6 (H26L)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3151954	NM_201431.2(RASSF6):c.59A>G (p.Tyr20Cys)	RASSF6 (Y20C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151953	NM_201431.2(RASSF6):c.46T>C (p.Ser16Pro)	RASSF6 (S16P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236675	NM_201431.2(RASSF6):c.44C>T (p.Ala15Val)	RASSF6 (A15V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617129	NM_201431.2(RASSF6):c.38C>G (p.Ala13Gly)	RASSF6 (A13G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151950	NM_201431.2(RASSF6):c.32C>A (p.Ala11Glu)	RASSF6 (A11E)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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: 37