"Ambry Genetics"[submitter] AND "SPDYC"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3168738	NM_001008778.3(SPDYC):c.-54C>T	SPDYC	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3168734	NM_001008778.3(SPDYC):c.-45A>G	SPDYC	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2301007	NM_001008778.3(SPDYC):c.-42C>T	SPDYC	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2495705	NM_001008778.3(SPDYC):c.29C>T (p.Ser10Phe)	SPDYC (S10F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379863	NM_001008778.3(SPDYC):c.100T>C (p.Phe34Leu)	SPDYC (F34L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168735	NM_001008778.3(SPDYC):c.133A>G (p.Ser45Gly)	SPDYC (S45G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399912	NM_001008778.3(SPDYC):c.170C>T (p.Ser57Phe)	SPDYC (S57F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535671	NM_001008778.3(SPDYC):c.305T>C (p.Met102Thr)	SPDYC (M102T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322056	NM_001008778.3(SPDYC):c.323G>A (p.Gly108Asp)	SPDYC (G108D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3168736	NM_001008778.3(SPDYC):c.355G>A (p.Gly119Arg)	SPDYC (G119R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168737	NM_001008778.3(SPDYC):c.374G>A (p.Arg125Gln)	SPDYC (R125Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2511768	NM_001008778.3(SPDYC):c.496C>T (p.Arg166Trp)	SPDYC (R166W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322055	NM_001008778.3(SPDYC):c.502C>T (p.Arg168Trp)	SPDYC (R168W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168739	NM_001008778.3(SPDYC):c.503G>A (p.Arg168Gln)	SPDYC (R168Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590791	NM_001008778.3(SPDYC):c.506G>A (p.Arg169His)	SPDYC (R169H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357458	NM_001008778.3(SPDYC):c.524T>G (p.Val175Gly)	SPDYC (V175G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361113	NM_001008778.3(SPDYC):c.553C>T (p.Arg185Cys)	SPDYC (R185C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278001	NM_001008778.3(SPDYC):c.613C>T (p.His205Tyr)	SPDYC (H205Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524440	NM_001008778.3(SPDYC):c.679C>T (p.Arg227Cys)	SPDYC (R227C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541866	NM_001008778.3(SPDYC):c.695A>C (p.Asn232Thr)	SPDYC (N232T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256608	NM_001008778.3(SPDYC):c.764T>C (p.Leu255Pro)	SPDYC (L255P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21