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

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2463201	NM_020407.5(RHBG):c.7G>C (p.Gly3Arg)	RHBG (G3R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2400720	NM_020407.5(RHBG):c.58C>T (p.Leu20Phe)	RHBG (L20F)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2246119	NM_020407.5(RHBG):c.103C>T (p.Arg35Cys)	RHBG (R35C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2339281	NM_020407.5(RHBG):c.130C>G (p.Leu44Val)	RHBG (L44V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2388953	NM_020407.5(RHBG):c.197A>G (p.Asp66Gly)	RHBG (D66G +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2245357	NM_020407.5(RHBG):c.229T>G (p.Phe77Val)	RHBG (F77V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314194	NM_020407.5(RHBG):c.235A>G (p.Met79Val)	RHBG (M10V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256804	NM_020407.5(RHBG):c.256G>A (p.Gly86Ser)	RHBG (G17S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487272	NM_020407.5(RHBG):c.403G>A (p.Ala135Thr)	RHBG (A135T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154018	NM_020407.5(RHBG):c.409C>G (p.Leu137Val)	RHBG (L137V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233316	NM_020407.5(RHBG):c.472C>A (p.Leu158Met)	RHBG (L128M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154019	NM_020407.5(RHBG):c.550A>T (p.Thr184Ser)	RHBG (T184S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244591	NM_020407.5(RHBG):c.563T>G (p.Phe188Cys)	RHBG (F158C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532397	NM_020407.5(RHBG):c.589T>C (p.Ser197Pro)	RHBG (S167P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314191	NM_020407.5(RHBG):c.610C>G (p.Gln204Glu)	RHBG (Q174E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401721	NM_020407.5(RHBG):c.748A>T (p.Thr250Ser)	RHBG (T220S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409239	NM_020407.5(RHBG):c.752C>T (p.Ala251Val)	RHBG (A251V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216407	NM_020407.5(RHBG):c.860C>T (p.Ala287Val)	RHBG (A218V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154020	NM_020407.5(RHBG):c.903G>A (p.Met301Ile)	RHBG (M232I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558921	NM_020407.5(RHBG):c.934T>A (p.Phe312Ile)	RHBG (F282I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224522	NM_020407.5(RHBG):c.977C>T (p.Thr326Met)	RHBG (T296M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603015	NM_020407.5(RHBG):c.1054G>A (p.Gly352Arg)	RHBG (G283R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455365	NM_020407.5(RHBG):c.1073T>C (p.Leu358Pro)	RHBG (L328P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455031	NM_020407.5(RHBG):c.1108G>A (p.Asp370Asn)	RHBG (D370N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314195	NM_020407.5(RHBG):c.1111G>A (p.Gly371Ser)	RHBG (G341S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154015	NM_020407.5(RHBG):c.1136T>C (p.Ile379Thr)	RHBG (I379T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403660	NM_020407.5(RHBG):c.1141G>C (p.Glu381Gln)	RHBG (E312Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154016	NM_020407.5(RHBG):c.1148A>G (p.Gln383Arg)	RHBG (Q353R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298794	NM_020407.5(RHBG):c.1186G>A (p.Gly396Arg)	RHBG (G327R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372336	NM_020407.5(RHBG):c.1222G>C (p.Gly408Arg)	RHBG (G339R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362060	NM_020407.5(RHBG):c.1225G>A (p.Gly409Ser)	RHBG (G340S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2325931	NM_020407.5(RHBG):c.1232G>A (p.Gly411Glu)	RHBG (G411E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154017	NM_020407.5(RHBG):c.1246A>G (p.Lys416Glu)	RHBG (K347E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314193	NM_020407.5(RHBG):c.1270C>G (p.Pro424Ala)	RHBG (P424A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591438	NM_020407.5(RHBG):c.1271C>G (p.Pro424Arg)	RHBG (P355R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517096	NM_020407.5(RHBG):c.1271C>A (p.Pro424Gln)	RHBG (P355H +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 36