"Ambry Genetics"[submitter] AND "H2BC10"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3283322	NM_003525.3(H2BC10):c.31C>T (p.Pro11Ser)	H2BC10, LOC129996044 (P11S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588450	NM_003525.3(H2BC10):c.31C>G (p.Pro11Ala)	H2BC10, LOC129996044 (P11A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103777	NM_003525.3(H2BC10):c.72G>C (p.Lys24Asn)	H2BC10, LOC129996044 (K24N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462922	NM_003525.3(H2BC10):c.73A>G (p.Lys25Glu)	H2BC10, LOC129996044 (K25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103778	NM_003525.3(H2BC10):c.88C>G (p.Arg30Gly)	H2BC10, LOC129996044 (R30G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552724	NM_003525.3(H2BC10):c.110G>C (p.Ser37Thr)	H2BC10, LOC129996044 (S37T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624270	NM_003525.3(H2BC10):c.157A>G (p.Thr53Ala)	H2BC10, LOC129996044 (T53A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103775	NM_003525.3(H2BC10):c.199G>C (p.Val67Leu)	H2BC10, LOC129996044 (V67L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103776	NM_003525.3(H2BC10):c.204C>G (p.Asn68Lys)	H2BC10, LOC129996044 (N68K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525499	NM_003525.3(H2BC10):c.288A>C (p.Gln96His)	H2BC10, LOC129996045 (Q96H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620073	NM_003525.3(H2BC10):c.302T>C (p.Leu101Pro)	H2BC10, LOC129996045 (L101P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283321	NM_003525.3(H2BC10):c.371G>A (p.Ser124Asn)	H2BC10, LOC129996045 (S124N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance