"Ambry Genetics"[submitter] AND "SPAG4"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2214249	NM_003116.3(SPAG4):c.32C>T (p.Ser11Leu)	LOC130065763, SPAG4 (S11L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2599029	NM_003116.3(SPAG4):c.52C>T (p.Pro18Ser)	LOC130065763, SPAG4 (P18S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3168058	NM_003116.3(SPAG4):c.139C>T (p.Pro47Ser)	LOC130065763, SPAG4 (P47S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2302339	NM_003116.3(SPAG4):c.160G>A (p.Gly54Ser)	LOC130065763, SPAG4 (G54S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2548660	NM_003116.3(SPAG4):c.257A>G (p.Asn86Ser)	LOC130065763, SPAG4 (N86S)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2242808	NM_003116.3(SPAG4):c.389G>C (p.Arg130Pro)	LOC130065764, SPAG4 (R130P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168059	NM_003116.3(SPAG4):c.470T>C (p.Met157Thr)	SPAG4 (M80T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301663	NM_003116.3(SPAG4):c.539C>T (p.Ala180Val)	SPAG4 (A103V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168060	NM_003116.3(SPAG4):c.774C>G (p.Asp258Glu)	SPAG4 (D181E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555462	NM_003116.3(SPAG4):c.797C>T (p.Ala266Val)	SPAG4 (A189V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598522	NM_003116.3(SPAG4):c.940T>A (p.Phe314Ile)	SPAG4 (F314I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168056	NM_003116.3(SPAG4):c.1025G>A (p.Ser342Asn)	SPAG4 (S342N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280977	NM_003116.3(SPAG4):c.1069G>C (p.Ala357Pro)	SPAG4 (A357P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259644	NM_003116.3(SPAG4):c.1081C>T (p.Leu361Phe)	SPAG4 (L361F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168057	NM_003116.3(SPAG4):c.1093G>A (p.Asp365Asn)	SPAG4 (D288N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479500	NM_003116.3(SPAG4):c.1189C>T (p.Pro397Ser)	SPAG4 (P320S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245881	NM_003116.3(SPAG4):c.1231C>T (p.Arg411Cys)	SPAG4 (R334C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460012	NM_003116.3(SPAG4):c.1307C>T (p.Pro436Leu)	SPAG4 (P359L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance