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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2322982	NM_002099.8(GYPA):c.433C>A (p.Pro145Thr)	GYPA (P112T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103371	NM_002099.8(GYPA):c.365C>T (p.Pro122Leu)	GYPA (P122L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488847	NM_002099.8(GYPA):c.364C>T (p.Pro122Ser)	GYPA (P109S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2604775	NM_002099.8(GYPA):c.347G>T (p.Arg116Leu)	GYPA (R83L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621490	NM_002099.8(GYPA):c.343C>A (p.Arg115Ser)	GYPA (R115S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103370	NM_002099.8(GYPA):c.337G>A (p.Gly113Ser)	GYPA (G100S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283203	NM_002099.8(GYPA):c.305G>A (p.Gly102Asp)	GYPA (G102D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283204	NM_002099.8(GYPA):c.281T>G (p.Leu94Arg)	GYPA (L94R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526468	NM_002099.8(GYPA):c.251C>T (p.Ala84Val)	GYPA (A84V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2307984	NM_002099.8(GYPA):c.205A>G (p.Thr69Ala)	GYPA (T69A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270806	NM_002099.8(GYPA):c.169C>A (p.Pro57Thr)	GYPA (P24T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103372	NM_002099.8(GYPA):c.80T>C (p.Met27Thr)	GYPA (M27T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2380498	NM_002099.8(GYPA):c.68C>A (p.Thr23Asn)	GYPA (T23N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance