ClinVar Miner

List of variants in gene CHST3 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004273.5(CHST3):c.959C>G (p.Thr320Ser) rs535309495 0.00077
NM_004273.5(CHST3):c.1135C>T (p.Leu379=) rs564028722 0.00049
NM_004273.5(CHST3):c.348G>T (p.Glu116Asp) rs144885813 0.00048
NM_004273.5(CHST3):c.528G>A (p.Pro176=) rs373748456 0.00039
NM_004273.5(CHST3):c.1363C>G (p.Leu455Val) rs374954414 0.00018
NM_004273.5(CHST3):c.114C>T (p.Ile38=) rs374590185 0.00016
NM_004273.5(CHST3):c.570C>T (p.Asp190=) rs367857089 0.00013
NM_004273.5(CHST3):c.423G>A (p.Thr141=) rs376107245 0.00011
NM_004273.5(CHST3):c.624G>A (p.Thr208=) rs145440508 0.00006
NM_004273.5(CHST3):c.540C>T (p.Asn180=) rs748812857 0.00004
NM_004273.5(CHST3):c.306C>A (p.Gly102=) rs776007496 0.00003
NM_004273.5(CHST3):c.447C>T (p.Gly149=) rs995812238 0.00003
NM_004273.5(CHST3):c.1056G>C (p.Ala352=) rs779966805 0.00002
NM_004273.5(CHST3):c.111C>T (p.Phe37=) rs371428228 0.00001
NM_004273.5(CHST3):c.1134G>A (p.Pro378=) rs893941954 0.00001
NM_004273.5(CHST3):c.1167C>T (p.Ala389=) rs1380183951 0.00001
NM_004273.5(CHST3):c.486C>T (p.Phe162=) rs774188997 0.00001
NM_004273.5(CHST3):c.72C>T (p.Tyr24=) rs542040061 0.00001
NM_004273.5(CHST3):c.861C>G (p.Ala287=) rs1489540204 0.00001
NM_004273.5(CHST3):c.942C>T (p.Phe314=) rs1010927640 0.00001
NM_004273.5(CHST3):c.1017G>A (p.Gln339=)
NM_004273.5(CHST3):c.1060C>T (p.Leu354=)
NM_004273.5(CHST3):c.1128C>T (p.Arg376=)
NM_004273.5(CHST3):c.1143G>A (p.Lys381=) rs2131776355
NM_004273.5(CHST3):c.1185G>A (p.Pro395=) rs1455730645
NM_004273.5(CHST3):c.1185G>T (p.Pro395=)
NM_004273.5(CHST3):c.1251G>A (p.Thr417=)
NM_004273.5(CHST3):c.1254G>A (p.Gln418=)
NM_004273.5(CHST3):c.1260C>T (p.Asn420=)
NM_004273.5(CHST3):c.1263C>G (p.Ser421=)
NM_004273.5(CHST3):c.1263C>T (p.Ser421=)
NM_004273.5(CHST3):c.1266G>A (p.Ser422=) rs372291815
NM_004273.5(CHST3):c.1275C>T (p.Phe425=)
NM_004273.5(CHST3):c.1293C>T (p.Ser431=)
NM_004273.5(CHST3):c.1326C>T (p.Ala442=)
NM_004273.5(CHST3):c.1332C>T (p.Cys444=)
NM_004273.5(CHST3):c.1350C>G (p.Leu450=)
NM_004273.5(CHST3):c.1365G>A (p.Leu455=)
NM_004273.5(CHST3):c.1368G>C (p.Ala456=)
NM_004273.5(CHST3):c.1380C>T (p.Ala460=) rs369055984
NM_004273.5(CHST3):c.1404C>T (p.Ser468=)
NM_004273.5(CHST3):c.1408C>T (p.Leu470=)
NM_004273.5(CHST3):c.141-14C>T
NM_004273.5(CHST3):c.141-17C>T
NM_004273.5(CHST3):c.168C>G (p.Pro56=) rs1840047159
NM_004273.5(CHST3):c.175C>T (p.Leu59=)
NM_004273.5(CHST3):c.195C>T (p.Thr65=) rs759935618
NM_004273.5(CHST3):c.201A>T (p.Pro67=)
NM_004273.5(CHST3):c.243C>T (p.Ser81=)
NM_004273.5(CHST3):c.255A>T (p.Ser85=)
NM_004273.5(CHST3):c.279T>C (p.Arg93=)
NM_004273.5(CHST3):c.306C>T (p.Gly102=) rs776007496
NM_004273.5(CHST3):c.327C>T (p.Ala109=)
NM_004273.5(CHST3):c.348G>A (p.Glu116=) rs144885813
NM_004273.5(CHST3):c.360G>A (p.Glu120=)
NM_004273.5(CHST3):c.36G>A (p.Arg12=)
NM_004273.5(CHST3):c.378G>C (p.Pro126=)
NM_004273.5(CHST3):c.378G>T (p.Pro126=)
NM_004273.5(CHST3):c.381C>T (p.Ala127=) rs769338504
NM_004273.5(CHST3):c.382G>C (p.Val128Leu) rs563761692
NM_004273.5(CHST3):c.384G>A (p.Val128=)
NM_004273.5(CHST3):c.480C>T (p.Tyr160=)
NM_004273.5(CHST3):c.48C>T (p.His16=) rs574784635
NM_004273.5(CHST3):c.492G>A (p.Pro164=)
NM_004273.5(CHST3):c.534C>T (p.Gly178=)
NM_004273.5(CHST3):c.549C>T (p.Gly183=)
NM_004273.5(CHST3):c.54G>T (p.Leu18=)
NM_004273.5(CHST3):c.552G>A (p.Ser184=)
NM_004273.5(CHST3):c.588C>T (p.Phe196=)
NM_004273.5(CHST3):c.594C>T (p.Cys198=)
NM_004273.5(CHST3):c.618C>T (p.Phe206=)
NM_004273.5(CHST3):c.633C>G (p.Pro211=)
NM_004273.5(CHST3):c.666G>C (p.Arg222=)
NM_004273.5(CHST3):c.681C>G (p.Ser227=) rs1840057937
NM_004273.5(CHST3):c.705G>C (p.Thr235=)
NM_004273.5(CHST3):c.711C>T (p.Phe237=)
NM_004273.5(CHST3):c.720G>A (p.Lys240=)
NM_004273.5(CHST3):c.759C>T (p.Gly253=)
NM_004273.5(CHST3):c.780C>T (p.Ala260=)
NM_004273.5(CHST3):c.795C>G (p.Arg265=)
NM_004273.5(CHST3):c.840G>A (p.Leu280=)
NM_004273.5(CHST3):c.849G>C (p.Leu283=)
NM_004273.5(CHST3):c.903C>G (p.Arg301=)
NM_004273.5(CHST3):c.906C>T (p.Asp302=)
NM_004273.5(CHST3):c.915C>A (p.Ala305=)
NM_004273.5(CHST3):c.945C>T (p.Ala315=)
NM_004273.5(CHST3):c.993C>T (p.Asp331=)

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.