"PreventionGenetics, part of Exact Sciences"[submitter] AND "HOXA13"[g - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033277	NM_000522.5(HOXA13):c.849C>T (p.Asn283=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 2634941	NM_000522.5(HOXA13):c.652G>A (p.Ala218Thr)	HOXA13, LOC107126288 (A218T)	Single nucleotide variant (missense variant)	HOXA13-related disorder	GUncertain significance
Select item 3047699	NM_000522.5(HOXA13):c.566A>G (p.Asn189Ser)	HOXA13, LOC107126288 (N189S)	Single nucleotide variant (missense variant)	HOXA13-related disorder	GUncertain significance
Select item 3054028	NM_000522.5(HOXA13):c.461G>A (p.Ser154Asn)	HOXA13, LOC107126288 (S154N)	Single nucleotide variant (missense variant)	HOXA13-related disorder	GUncertain significance
Select item 1685262	NM_000522.5(HOXA13):c.381CGC[5] (p.Ala133del)	HOXA13, LOC107126288 (A133del)	Microsatellite (inframe_deletion)	not specified +1 more	GBenign/Likely benign
Select item 591788	NM_000522.5(HOXA13):c.357_395del (p.Ala121_Ala133del)	HOXA13, LOC107126288	Deletion (inframe_deletion)	not provided +1 more	GUncertain significance
Select item 3036773	NM_000522.5(HOXA13):c.390C>A (p.Ala130=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 3030848	NM_000522.5(HOXA13):c.390C>G (p.Ala130=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 3036424	NM_000522.5(HOXA13):c.384C>G (p.Ala128=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 591433	NM_000522.5(HOXA13):c.360_377del (p.Ala128_Ala133del)	HOXA13, LOC107126288	Deletion (inframe_deletion)	not provided +3 more	GLikely benign
Select item 3040337	NM_000522.5(HOXA13):c.375T>G (p.Ala125=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 3037887	NM_000522.5(HOXA13):c.372C>A (p.Ala124=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 3036749	NM_000522.5(HOXA13):c.363C>G (p.Ala121=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 726530	NM_000522.5(HOXA13):c.342G>A (p.Pro114=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder +1 more	GLikely benign
Select item 3032454	NM_000522.5(HOXA13):c.228C>A (p.Ala76=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign
Select item 1672190	NM_000522.5(HOXA13):c.175C>G (p.Pro59Ala)	HOXA13, LOC107126288 (P59A)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3045014	NM_000522.5(HOXA13):c.135T>G (p.Ala45=)	HOXA13, LOC107126288	Single nucleotide variant (synonymous variant)	HOXA13-related disorder	GLikely benign