List of variants in gene GSR reported as uncertain significance for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000637.5(GSR):c.697C>T (p.Arg233Cys)	rs145851500	0.00037
NM_000637.5(GSR):c.878C>G (p.Ser293Cys)	rs762024253	0.00008
NM_000637.5(GSR):c.1334C>T (p.Thr445Met)	rs778165636	0.00006
NM_000637.5(GSR):c.859G>A (p.Val287Met)	rs750862066	0.00004
NM_000637.5(GSR):c.307G>A (p.Val103Met)	rs745404470	0.00001
NM_000637.5(GSR):c.1023C>G (p.Asp341Glu)
NM_000637.5(GSR):c.1054G>A (p.Asp352Asn)
NM_000637.5(GSR):c.1060A>G (p.Lys354Glu)
NM_000637.5(GSR):c.1081G>A (p.Glu361Lys)
NM_000637.5(GSR):c.1171C>T (p.Arg391Ter)
NM_000637.5(GSR):c.1196A>C (p.Glu399Ala)
NM_000637.5(GSR):c.1256C>T (p.Pro419Leu)
NM_000637.5(GSR):c.1358C>T (p.Ala453Val)
NM_000637.5(GSR):c.1486A>C (p.Lys496Gln)
NM_000637.5(GSR):c.1525G>A (p.Ala509Thr)
NM_000637.5(GSR):c.372T>C (p.His124=)
NM_000637.5(GSR):c.395C>T (p.Pro132Leu)
NM_000637.5(GSR):c.433G>A (p.Glu145Lys)
NM_000637.5(GSR):c.439C>G (p.Arg147Gly)	rs150594097
NM_000637.5(GSR):c.476A>T (p.Gln159Leu)
NM_000637.5(GSR):c.512G>T (p.Arg171Leu)	rs766106295
NM_000637.5(GSR):c.698G>A (p.Arg233His)	rs750234827
NM_000637.5(GSR):c.781A>G (p.Ile261Val)
NM_000637.5(GSR):c.815C>T (p.Ser272Leu)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.