ClinVar Miner

List of variants in gene FLVCR1 reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014053.4(FLVCR1):c.1657T>G (p.Ser553Ala) rs149887215 0.00064
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met) rs149834738 0.00032
NM_014053.4(FLVCR1):c.595C>T (p.Leu199Phe) rs41296694 0.00026
NM_014053.4(FLVCR1):c.1619A>G (p.Gln540Arg) rs144226457 0.00011
NM_014053.4(FLVCR1):c.554G>C (p.Cys185Ser) rs747064078 0.00010
NM_014053.4(FLVCR1):c.25G>A (p.Gly9Arg) rs916015252 0.00007
NM_014053.4(FLVCR1):c.901C>T (p.Arg301Trp) rs144013956 0.00005
NM_014053.4(FLVCR1):c.307C>T (p.Leu103Phe) rs769200783 0.00003
NM_014053.4(FLVCR1):c.580A>T (p.Ser194Cys) rs1274821663 0.00003
NM_014053.4(FLVCR1):c.1271A>G (p.Tyr424Cys) rs558398621 0.00001
NM_014053.4(FLVCR1):c.1457C>T (p.Ser486Leu) rs756375276 0.00001
NM_014053.4(FLVCR1):c.7C>T (p.Arg3Trp) rs998058913 0.00001
NM_014053.4(FLVCR1):c.1028T>C (p.Ile343Thr)
NM_014053.4(FLVCR1):c.1445G>A (p.Gly482Glu)
NM_014053.4(FLVCR1):c.1536G>C (p.Lys512Asn)
NM_014053.4(FLVCR1):c.369T>A (p.Phe123Leu) rs1189460003
NM_014053.4(FLVCR1):c.381G>C (p.Gln127His) rs1664123520
NM_014053.4(FLVCR1):c.665C>G (p.Ser222Cys)
NM_014053.4(FLVCR1):c.715G>C (p.Ala239Pro)
NM_014053.4(FLVCR1):c.886T>G (p.Phe296Val) rs1294845921
NM_014053.4(FLVCR1):c.938A>G (p.Asp313Gly)
NM_014053.4(FLVCR1):c.994A>C (p.Ile332Leu)

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.