ClinVar Miner

List of variants in gene FLVCR1 reported by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP
NM_014053.4(FLVCR1):c.-7C>T rs1323079807
NM_014053.4(FLVCR1):c.1015A>T (p.Ile339Phe) rs1558113016
NM_014053.4(FLVCR1):c.1022A>G (p.Tyr341Cys)
NM_014053.4(FLVCR1):c.1085A>G (p.Tyr362Cys) rs199842709
NM_014053.4(FLVCR1):c.1097A>T (p.Glu366Val) rs949984167
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met) rs149834738
NM_014053.4(FLVCR1):c.1272T>C (p.Tyr424=) rs17677416
NM_014053.4(FLVCR1):c.1406C>G (p.Ser469Cys)
NM_014053.4(FLVCR1):c.143C>T (p.Pro48Leu)
NM_014053.4(FLVCR1):c.154G>C (p.Ala52Pro) rs11120047
NM_014053.4(FLVCR1):c.1554_1555del (p.His518fs) rs777543198
NM_014053.4(FLVCR1):c.1561_1564del (p.Ile520_Asn521insTer) rs1572031494
NM_014053.4(FLVCR1):c.1593+9T>C rs17019870
NM_014053.4(FLVCR1):c.1619A>G (p.Gln540Arg) rs144226457
NM_014053.4(FLVCR1):c.1624C>T (p.Pro542Ser) rs141575859
NM_014053.4(FLVCR1):c.1631C>T (p.Thr544Met) rs3207090
NM_014053.4(FLVCR1):c.1642del (p.Ser548fs) rs766024598
NM_014053.4(FLVCR1):c.1657T>G (p.Ser553Ala) rs149887215
NM_014053.4(FLVCR1):c.169C>G (p.Leu57Val)
NM_014053.4(FLVCR1):c.18T>A (p.Asp6Glu)
NM_014053.4(FLVCR1):c.267G>A (p.Glu89=) rs1553261817
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=)
NM_014053.4(FLVCR1):c.364G>A (p.Ala122Thr) rs1553261879
NM_014053.4(FLVCR1):c.391A>G (p.Ile131Val) rs1558104917
NM_014053.4(FLVCR1):c.488C>T (p.Pro163Leu) rs369434267
NM_014053.4(FLVCR1):c.49C>G (p.Pro17Ala) rs543847452
NM_014053.4(FLVCR1):c.595C>T (p.Leu199Phe) rs41296694
NM_014053.4(FLVCR1):c.663C>T (p.Pro221=)
NM_014053.4(FLVCR1):c.71C>T (p.Pro24Leu) rs562153726
NM_014053.4(FLVCR1):c.738+9T>C rs41296696
NM_014053.4(FLVCR1):c.785A>G (p.Asn262Ser) rs547679833
NM_014053.4(FLVCR1):c.799A>G (p.Thr267Ala) rs1558107949
NM_014053.4(FLVCR1):c.819T>C (p.Asn273=) rs1558107967
NM_014053.4(FLVCR1):c.937G>A (p.Asp313Asn) rs139175550
NM_014053.4(FLVCR1):c.952G>A (p.Glu318Lys) rs41297444
NM_014053.4(FLVCR1):c.987T>G (p.Phe329Leu) rs762546149

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.