Related gene-specific medical variations for Gene (Select 8343) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3283337	NM_003522.4(H2BC7):c.284T>C (p.Ile95Thr)	H2BC7, LOC126859627 (I95T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103842	NM_003522.4(H2BC7):c.89G>A (p.Arg30His)	H2BC7, LOC126859627 (R30H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103841	NM_003522.4(H2BC7):c.59C>G (p.Thr20Ser)	H2BC7, LOC126859627 (T20S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103840	NM_003522.4(H2BC7):c.298C>T (p.Arg100Cys)	H2BC7, LOC126859627 (R100C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103839	NM_003522.4(H2BC7):c.227G>T (p.Gly76Val)	H2BC7, LOC126859627 (G76V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103838	NM_003522.4(H2BC7):c.205G>C (p.Asp69His)	H2BC7, LOC126859627 (D69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103837	NM_003522.4(H2BC7):c.19T>C (p.Ser7Pro)	H2BC7, LOC126859627 (S7P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103836	NM_003522.4(H2BC7):c.17A>G (p.Lys6Arg)	H2BC7, LOC126859627 (K6R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103835	NM_003522.4(H2BC7):c.155A>C (p.Asp52Ala)	H2BC7, LOC126859627 (D52A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103834	NM_003522.4(H2BC7):c.11C>T (p.Pro4Leu)	H2BC7, LOC126859627 (P4L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656308	NM_003523.3(H2BC6):c.70AAG[1] (p.Lys25del)	H2BC7, H2BC6 (K25del)	Microsatellite (inframe_deletion)	not provided	GLikely benign
Select item 2596099	NM_003522.4(H2BC7):c.41G>C (p.Gly14Ala)	H2BC7, LOC126859627 (G14A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515853	NM_003522.4(H2BC7):c.73A>C (p.Lys25Gln)	H2BC7, LOC126859627 (K25Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance