Related gene-specific medical variations for Gene (Select 57715) - ClinVar

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Links from Gene

Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3159850	NM_017893.4(SEMA4G):c.785G>A (p.Arg262His)	MRPL43, SEMA4G (R184W +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3159849	NM_017893.4(SEMA4G):c.681C>G (p.Ser227Arg)	MRPL43, SEMA4G (A261P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159848	NM_017893.4(SEMA4G):c.506G>A (p.Arg169His)	MRPL43, SEMA4G (R169H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159843	NM_017893.4(SEMA4G):c.2520G>C (p.Glu840Asp)	MRPL43, SEMA4G (E835D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159842	NM_017893.4(SEMA4G):c.2420G>A (p.Ser807Asn)	MRPL43, SEMA4G (S802N +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159839	NM_017893.4(SEMA4G):c.2062G>A (p.Ala688Thr)	MRPL43, SEMA4G (A683T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159838	NM_017893.4(SEMA4G):c.1870G>C (p.Val624Leu)	MRPL43, SEMA4G (V619L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159837	NM_017893.4(SEMA4G):c.1742G>C (p.Arg581Pro)	MRPL43, SEMA4G (R581P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159836	NM_017893.4(SEMA4G):c.1603G>A (p.Ala535Thr)	MRPL43, SEMA4G (A535T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159835	NM_017893.4(SEMA4G):c.1078C>T (p.Arg360Trp)	MRPL43, SEMA4G (R360W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159834	NM_017893.4(SEMA4G):c.1039G>A (p.Val347Ile)	MRPL43, SEMA4G (V347I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159833	NM_017893.4(SEMA4G):c.1024G>A (p.Ala342Thr)	MRPL43, SEMA4G (A342T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2616578	NM_017893.4(SEMA4G):c.1562G>A (p.Arg521Gln)	MRPL43, SEMA4G (R521Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2588588	NM_017893.4(SEMA4G):c.902C>T (p.Thr301Ile)	MRPL43, SEMA4G (T301I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2588082	NM_017893.4(SEMA4G):c.1249C>T (p.Arg417Trp)	MRPL43, SEMA4G (R417W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2526716	NM_017893.4(SEMA4G):c.1741C>T (p.Arg581Trp)	MRPL43, SEMA4G (R576W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2508028	NM_017893.4(SEMA4G):c.1067A>T (p.Gln356Leu)	MRPL43, SEMA4G (Q356L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2507893	NM_017893.4(SEMA4G):c.446C>A (p.Ala149Asp)	MRPL43, SEMA4G (A149D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2482530	NM_017893.4(SEMA4G):c.1741C>G (p.Arg581Gly)	MRPL43, SEMA4G (R581G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2479882	NM_017893.4(SEMA4G):c.1730G>A (p.Arg577His)	MRPL43, SEMA4G (R572H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2464682	NM_017893.4(SEMA4G):c.586C>T (p.Arg196Trp)	MRPL43, SEMA4G (R196W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2463227	NM_017893.4(SEMA4G):c.2471G>A (p.Arg824His)	MRPL43, SEMA4G (R819H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2460552	NM_017893.4(SEMA4G):c.1709C>T (p.Pro570Leu)	MRPL43, SEMA4G (P570L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459525	NM_017893.4(SEMA4G):c.2177G>A (p.Gly726Glu)	MRPL43, SEMA4G (G721E +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2459141	NM_017893.4(SEMA4G):c.1940T>C (p.Leu647Pro)	MRPL43, SEMA4G (L642P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2402723	NM_017893.4(SEMA4G):c.2495C>G (p.Thr832Arg)	MRPL43, SEMA4G (T832R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2400441	NM_017893.4(SEMA4G):c.535G>A (p.Gly179Ser)	MRPL43, SEMA4G (G179S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2399230	NM_017893.4(SEMA4G):c.628A>G (p.Met210Val)	SEMA4G, MRPL43 (M210V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2398527	NM_017893.4(SEMA4G):c.1094A>G (p.Tyr365Cys)	MRPL43, SEMA4G (Y365C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2379184	NM_017893.4(SEMA4G):c.1088G>A (p.Gly363Asp)	MRPL43, SEMA4G (G363D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2371323	NM_017893.4(SEMA4G):c.1592C>A (p.Thr531Asn)	MRPL43, SEMA4G (T531N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2366290	NM_017893.4(SEMA4G):c.1495G>A (p.Gly499Arg)	MRPL43, SEMA4G (G499R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2365609	NM_017893.4(SEMA4G):c.1036G>A (p.Ala346Thr)	MRPL43, SEMA4G (A346T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2361658	NM_017893.4(SEMA4G):c.474G>C (p.Glu158Asp)	MRPL43, SEMA4G (E158D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2348422	NM_017893.4(SEMA4G):c.505C>T (p.Arg169Cys)	SEMA4G, MRPL43 (R169C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2340642	NM_017893.4(SEMA4G):c.1817T>C (p.Met606Thr)	MRPL43, SEMA4G (M601T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2327698	NM_017893.4(SEMA4G):c.1997C>G (p.Ala666Gly)	MRPL43, SEMA4G (A661G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2300846	NM_017893.4(SEMA4G):c.2080C>T (p.Leu694Phe)	MRPL43, SEMA4G (L694F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2289874	NM_017893.4(SEMA4G):c.986A>G (p.Lys329Arg)	MRPL43, SEMA4G (K329R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2284890	NM_017893.4(SEMA4G):c.670G>A (p.Val224Met)	MRPL43, SEMA4G (V224M)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2280445	NM_017893.4(SEMA4G):c.1814G>T (p.Ser605Ile)	MRPL43, SEMA4G (S600I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2268942	NM_017893.4(SEMA4G):c.1933C>T (p.Arg645Cys)	MRPL43, SEMA4G (R645C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2267441	NM_017893.4(SEMA4G):c.979C>G (p.Gln327Glu)	MRPL43, SEMA4G (V212L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2239683	NM_017893.4(SEMA4G):c.1828G>A (p.Asp610Asn)	MRPL43, SEMA4G (D605N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2215669	NM_017893.4(SEMA4G):c.1846C>T (p.Arg616Cys)	MRPL43, SEMA4G (R611C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 788432	NM_017893.4(SEMA4G):c.1501A>G (p.Ile501Val)	MRPL43, SEMA4G (I501V)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 785328	NM_017893.4(SEMA4G):c.1632C>T (p.Ser544=)	MRPL43, SEMA4G	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 785327	NM_017893.4(SEMA4G):c.1374C>T (p.Ala458=)	MRPL43, SEMA4G	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 770208	NM_017893.4(SEMA4G):c.891A>G (p.Pro297=)	SEMA4G, MRPL43	Single nucleotide variant (synonymous variant +3 more)	not provided	GBenign
Select item 724462	NM_017893.4(SEMA4G):c.1789C>T (p.Arg597Trp)	MRPL43, SEMA4G (R597W +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 723350	NM_017893.4(SEMA4G):c.2162G>A (p.Arg721Gln)	MRPL43, SEMA4G (R721Q +2 more)	Single nucleotide variant (missense variant +4 more)	not provided	GLikely benign

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Links from Gene

Items: 51