"Ambry Genetics"[submitter] AND "H3-4"[gene] - ClinVar

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Search results

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2533932	NM_003493.3(H3-4):c.403C>T (p.Arg135Trp)	H3-4 (R135W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103894	NM_003493.3(H3-4):c.349C>T (p.Arg117Trp)	H3-4 (R117W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103893	NM_003493.3(H3-4):c.289T>A (p.Cys97Ser)	H3-4 (C97S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103890	NM_003493.3(H3-4):c.224T>A (p.Ile75Asn)	H3-4 (I75N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103889	NM_003493.3(H3-4):c.217C>G (p.Arg73Gly)	H3-4 (R73G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103888	NM_003493.3(H3-4):c.215T>C (p.Met72Thr)	H3-4 (M72T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283346	NM_003493.3(H3-4):c.190C>G (p.Arg64Gly)	H3-4 (R64G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570068	NM_003493.3(H3-4):c.161G>A (p.Arg54His)	H3-4 (R54H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283350	NM_003493.3(H3-4):c.158G>A (p.Arg53His)	H3-4 (R53H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103887	NM_003493.3(H3-4):c.157C>A (p.Arg53Ser)	H3-4 (R53S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103886	NM_003493.3(H3-4):c.131C>G (p.Pro44Arg)	H3-4 (P44R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534529	NM_003493.3(H3-4):c.125A>G (p.Tyr42Cys)	H3-4 (Y42C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103885	NM_003493.3(H3-4):c.118C>T (p.His40Tyr)	H3-4 (H40Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283347	NM_003493.3(H3-4):c.107T>C (p.Val36Ala)	H3-4 (V36A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103897	NM_003493.3(H3-4):c.95C>A (p.Ala32Asp)	H3-4 (A32D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103896	NM_003493.3(H3-4):c.92C>T (p.Pro31Leu)	H3-4 (P31L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103895	NM_003493.3(H3-4):c.83A>G (p.Lys28Arg)	H3-4 (K28R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525028	NM_003493.3(H3-4):c.53G>A (p.Arg18His)	H3-4 (R18H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103892	NM_003493.3(H3-4):c.26G>C (p.Arg9Pro)	H3-4 (R9P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598796	NM_003493.3(H3-4):c.25C>T (p.Arg9Cys)	H3-4 (R9C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103891	NM_003493.3(H3-4):c.23C>T (p.Ala8Val)	H3-4 (A8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604732	NM_003493.3(H3-4):c.11C>G (p.Thr4Ser)	H3-4 (T4S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22