GSG1L[gene] and "single gene"[properties] - ClinVar - NCBI

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

Search results

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102909	NM_001109763.2(GSG1L):c.965G>A (p.Arg322Gln)	GSG1L (R340Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599643	NM_001109763.2(GSG1L):c.883G>A (p.Glu295Lys)	GSG1L (E244K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282984	NM_001109763.2(GSG1L):c.880C>T (p.His294Tyr)	GSG1L (H139Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514204	NM_001109763.2(GSG1L):c.869T>C (p.Leu290Ser)	GSG1L (L239S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514013	NM_001109763.2(GSG1L):c.847G>A (p.Gly283Arg)	GSG1L (G232R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257946	NM_001109763.2(GSG1L):c.823C>T (p.Arg275Trp)	GSG1L (R275W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481568	NM_001109763.2(GSG1L):c.821T>C (p.Phe274Ser)	GSG1L (F119S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483384	NM_001109763.2(GSG1L):c.731C>T (p.Thr244Met)	GSG1L (T193M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102908	NM_001109763.2(GSG1L):c.710C>T (p.Thr237Met)	GSG1L (T237M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462050	NM_001109763.2(GSG1L):c.607A>G (p.Ser203Gly)	GSG1L (S152G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305155	NM_001109763.2(GSG1L):c.517A>G (p.Asn173Asp)	GSG1L (N173D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102907	NM_001109763.2(GSG1L):c.484C>T (p.His162Tyr)	GSG1L (H162Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490948	NM_001109763.2(GSG1L):c.475G>A (p.Glu159Lys)	GSG1L (E159K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346322	NM_001109763.2(GSG1L):c.245C>G (p.Pro82Arg)	GSG1L (P82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance