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

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314199	NM_016321.3(RHCG):c.1430T>G (p.Leu477Trp)	RHCG (L477W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462038	NM_016321.3(RHCG):c.1421C>T (p.Ser474Leu)	RHCG (S474L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408625	NM_016321.3(RHCG):c.1355C>T (p.Thr452Ile)	RHCG (T452I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284636	NM_016321.3(RHCG):c.1326C>G (p.Asn442Lys)	RHCG (N442K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2590665	NM_016321.3(RHCG):c.1265G>T (p.Gly422Val)	RHCG (G422V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291350	NM_016321.3(RHCG):c.1255C>T (p.Pro419Ser)	RHCG (P419S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552911	NM_016321.3(RHCG):c.1183A>G (p.Ile395Val)	RHCG (I395V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363760	NM_016321.3(RHCG):c.1147G>A (p.Gly383Arg)	RHCG (G383R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2345852	NM_016321.3(RHCG):c.1138G>A (p.Gly380Ser)	RHCG (G380S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314200	NM_016321.3(RHCG):c.1076C>T (p.Ala359Val)	RHCG (A359V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244251	NM_016321.3(RHCG):c.1039C>T (p.Pro347Ser)	RHCG (P347S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206703	NM_016321.3(RHCG):c.1012T>G (p.Cys338Gly)	RHCG (C338G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154037	NM_016321.3(RHCG):c.991C>T (p.Arg331Trp)	RHCG (R331W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388155	NM_016321.3(RHCG):c.946A>G (p.Ile316Val)	RHCG (I316V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3314202	NM_016321.3(RHCG):c.944T>C (p.Ile315Thr)	RHCG (I315T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363370	NM_016321.3(RHCG):c.940G>A (p.Gly314Ser)	RHCG (G314S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154036	NM_016321.3(RHCG):c.928G>A (p.Gly310Ser)	RHCG (G310S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208950	NM_016321.3(RHCG):c.887C>T (p.Ala296Val)	RHCG (A296V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398263	NM_016321.3(RHCG):c.877G>T (p.Val293Leu)	RHCG (V293L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154035	NM_016321.3(RHCG):c.859C>T (p.Leu287Phe)	RHCG (L287F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154034	NM_016321.3(RHCG):c.781G>A (p.Val261Met)	RHCG (V261M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154033	NM_016321.3(RHCG):c.738G>C (p.Gln246His)	RHCG (Q246H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333041	NM_016321.3(RHCG):c.607A>C (p.Asn203His)	RHCG (N203H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524114	NM_016321.3(RHCG):c.605G>A (p.Arg202His)	RHCG (R202H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405140	NM_016321.3(RHCG):c.583G>A (p.Val195Met)	RHCG (V195M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154032	NM_016321.3(RHCG):c.487G>A (p.Ala163Thr)	RHCG (A163T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154031	NM_016321.3(RHCG):c.346C>T (p.Arg116Cys)	RHCG (R116C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211711	NM_016321.3(RHCG):c.274A>G (p.Asn92Asp)	RHCG (N92D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154030	NM_016321.3(RHCG):c.259A>T (p.Ser87Cys)	RHCG (S87C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236677	NM_016321.3(RHCG):c.220T>C (p.Phe74Leu)	RHCG (F74L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482804	NM_016321.3(RHCG):c.191A>G (p.Gln64Arg)	RHCG (Q64R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212479	NM_016321.3(RHCG):c.173A>G (p.Tyr58Cys)	RHCG (Y58C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260628	NM_016321.3(RHCG):c.142A>G (p.Asn48Asp)	RHCG (N48D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314201	NM_016321.3(RHCG):c.127G>C (p.Glu43Gln)	RHCG (E43Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154028	NM_016321.3(RHCG):c.121T>C (p.Trp41Arg)	RHCG (W41R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456217	NM_016321.3(RHCG):c.89T>C (p.Val30Ala)	RHCG (V30A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546780	NM_016321.3(RHCG):c.37C>T (p.Leu13Phe)	RHCG (L13F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210661	NM_016321.3(RHCG):c.14C>T (p.Thr5Ile)	RHCG (T5I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 38