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

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103379	NM_002101.5(GYPC):c.46C>T (p.Leu16Phe)	GYPC, LOC129934706 (L16F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2689187	NM_002101.5(GYPC):c.150G>C (p.Glu50Asp)	GYPC (E29D +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1693821	NM_002101.5(GYPC):c.167T>A (p.Ile56Lys)	GYPC (I35K +2 more)	Single nucleotide variant (missense variant)	Blood group, Gerbich system +2 more	GUncertain significance
Select item 2327104	NM_002101.5(GYPC):c.172G>A (p.Asp58Asn)	GYPC (D37N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103376	NM_002101.5(GYPC):c.179T>C (p.Val60Ala)	GYPC (V60A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2218146	NM_002101.5(GYPC):c.211A>G (p.Ile71Val)	GYPC (I71V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103377	NM_002101.5(GYPC):c.235G>A (p.Val79Ile)	GYPC (V60I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283205	NM_002101.5(GYPC):c.256C>T (p.Arg86Trp)	GYPC (R67W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456954	NM_002101.5(GYPC):c.269C>T (p.Thr90Met)	GYPC (T71M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466417	NM_002101.5(GYPC):c.296C>T (p.Thr99Met)	GYPC (T78M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance