ClinVar Miner

List of variants in gene FLVCR1 reported by Invitae

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Gene type:
ClinVar version:
Total variants: 124
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HGVS dbSNP
NC_000001.10:g.(?_213058615)_(213058758_?)del
NC_000001.11:g.(?_212894986)_(212895290_?)dup
NM_014053.4(FLVCR1):c.1017C>T (p.Ile339=)
NM_014053.4(FLVCR1):c.1074G>T (p.Met358Ile)
NM_014053.4(FLVCR1):c.1085A>G (p.Tyr362Cys) rs199842709
NM_014053.4(FLVCR1):c.1092+5G>A rs556788423
NM_014053.4(FLVCR1):c.1093-12_1095del
NM_014053.4(FLVCR1):c.1093G>A (p.Gly365Arg)
NM_014053.4(FLVCR1):c.1096G>C (p.Glu366Gln)
NM_014053.4(FLVCR1):c.1097A>T (p.Glu366Val) rs949984167
NM_014053.4(FLVCR1):c.1097AAG[1] (p.Glu367del)
NM_014053.4(FLVCR1):c.112C>G (p.Leu38Val)
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met) rs149834738
NM_014053.4(FLVCR1):c.1168T>C (p.Leu390=)
NM_014053.4(FLVCR1):c.1197-4T>G
NM_014053.4(FLVCR1):c.1200G>T (p.Gln400His)
NM_014053.4(FLVCR1):c.1258T>C (p.Leu420=)
NM_014053.4(FLVCR1):c.1271A>G (p.Tyr424Cys)
NM_014053.4(FLVCR1):c.1272T>C (p.Tyr424=) rs17677416
NM_014053.4(FLVCR1):c.1282G>A (p.Val428Met)
NM_014053.4(FLVCR1):c.1284G>A (p.Val428=)
NM_014053.4(FLVCR1):c.1291dup (p.Thr431fs)
NM_014053.4(FLVCR1):c.1302G>C (p.Val434=)
NM_014053.4(FLVCR1):c.1307+14G>T
NM_014053.4(FLVCR1):c.1307+19T>A rs2291772
NM_014053.4(FLVCR1):c.133G>A (p.Gly45Ser) rs532977695
NM_014053.4(FLVCR1):c.1409C>T (p.Ala470Val)
NM_014053.4(FLVCR1):c.1413G>A (p.Gln471=)
NM_014053.4(FLVCR1):c.1414-11T>C
NM_014053.4(FLVCR1):c.1419T>C (p.Phe473=)
NM_014053.4(FLVCR1):c.1424T>C (p.Ile475Thr)
NM_014053.4(FLVCR1):c.1457C>T (p.Ser486Leu)
NM_014053.4(FLVCR1):c.1467T>C (p.Gly489=)
NM_014053.4(FLVCR1):c.1474G>T (p.Ala492Ser)
NM_014053.4(FLVCR1):c.1482C>A (p.Asn494Lys)
NM_014053.4(FLVCR1):c.1488dup (p.Leu497fs)
NM_014053.4(FLVCR1):c.1503G>A (p.Met501Ile)
NM_014053.4(FLVCR1):c.1521A>G (p.Leu507=) rs74607124
NM_014053.4(FLVCR1):c.1525+12C>T
NM_014053.4(FLVCR1):c.1547G>A (p.Arg516Gln)
NM_014053.4(FLVCR1):c.154G>C (p.Ala52Pro) rs11120047
NM_014053.4(FLVCR1):c.1559T>C (p.Ile520Thr)
NM_014053.4(FLVCR1):c.1567G>A (p.Gly523Arg)
NM_014053.4(FLVCR1):c.1572dup (p.Thr525fs)
NM_014053.4(FLVCR1):c.1593+5_1593+8del
NM_014053.4(FLVCR1):c.1593+9T>C rs17019870
NM_014053.4(FLVCR1):c.1594-10G>T
NM_014053.4(FLVCR1):c.1594-13_1594-10dup rs41301015
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.1626A>G (p.Pro542=) rs888869006
NM_014053.4(FLVCR1):c.1631C>T (p.Thr544Met) rs3207090
NM_014053.4(FLVCR1):c.1632G>A (p.Thr544=)
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.177C>T (p.Ala59=)
NM_014053.4(FLVCR1):c.178G>T (p.Ala60Ser)
NM_014053.4(FLVCR1):c.178_179delinsAT (p.Ala60Ile)
NM_014053.4(FLVCR1):c.198G>T (p.Gly66=)
NM_014053.4(FLVCR1):c.201T>C (p.Pro67=)
NM_014053.4(FLVCR1):c.202C>G (p.Gln68Glu)
NM_014053.4(FLVCR1):c.216C>A (p.Ala72=) rs1398603103
NM_014053.4(FLVCR1):c.254G>C (p.Gly85Ala)
NM_014053.4(FLVCR1):c.25G>A (p.Gly9Arg)
NM_014053.4(FLVCR1):c.26G>A (p.Gly9Glu)
NM_014053.4(FLVCR1):c.279C>A (p.Ala93=)
NM_014053.4(FLVCR1):c.279C>T (p.Ala93=)
NM_014053.4(FLVCR1):c.294G>T (p.Leu98=) rs376377158
NM_014053.4(FLVCR1):c.303G>C (p.Thr101=) rs1189185318
NM_014053.4(FLVCR1):c.306G>A (p.Ala102=)
NM_014053.4(FLVCR1):c.307C>T (p.Leu103Phe)
NM_014053.4(FLVCR1):c.322T>G (p.Phe108Val)
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=)
NM_014053.4(FLVCR1):c.361A>G (p.Asn121Asp) rs267606820
NM_014053.4(FLVCR1):c.362A>G (p.Asn121Ser)
NM_014053.4(FLVCR1):c.366C>T (p.Ala122=)
NM_014053.4(FLVCR1):c.369T>A (p.Phe123Leu)
NM_014053.4(FLVCR1):c.372G>A (p.Gln124=)
NM_014053.4(FLVCR1):c.398A>C (p.Asn133Thr)
NM_014053.4(FLVCR1):c.3G>T (p.Met1Ile) rs899735028
NM_014053.4(FLVCR1):c.40C>T (p.Pro14Ser)
NM_014053.4(FLVCR1):c.42C>T (p.Pro14=) rs886045923
NM_014053.4(FLVCR1):c.476C>G (p.Pro159Arg)
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.525C>T (p.Leu175=) rs755329362
NM_014053.4(FLVCR1):c.532C>T (p.Leu178=)
NM_014053.4(FLVCR1):c.551A>C (p.Asn184Thr)
NM_014053.4(FLVCR1):c.554G>C (p.Cys185Ser)
NM_014053.4(FLVCR1):c.563C>T (p.Ala188Val)
NM_014053.4(FLVCR1):c.593A>G (p.His198Arg)
NM_014053.4(FLVCR1):c.595C>T (p.Leu199Phe) rs41296694
NM_014053.4(FLVCR1):c.642G>C (p.Gln214His)
NM_014053.4(FLVCR1):c.663C>T (p.Pro221=)
NM_014053.4(FLVCR1):c.690G>A (p.Gly230=) rs1352757781
NM_014053.4(FLVCR1):c.692C>A (p.Pro231His)
NM_014053.4(FLVCR1):c.69C>T (p.Leu23=) rs374379789
NM_014053.4(FLVCR1):c.6G>A (p.Ala2=)
NM_014053.4(FLVCR1):c.700G>T (p.Val234Leu)
NM_014053.4(FLVCR1):c.71C>T (p.Pro24Leu) rs562153726
NM_014053.4(FLVCR1):c.738+10G>A
NM_014053.4(FLVCR1):c.738+9T>C rs41296696
NM_014053.4(FLVCR1):c.75G>A (p.Leu25=)
NM_014053.4(FLVCR1):c.768A>G (p.Pro256=) rs774690148
NM_014053.4(FLVCR1):c.7C>T (p.Arg3Trp) rs998058913
NM_014053.4(FLVCR1):c.820A>G (p.Ile274Val)
NM_014053.4(FLVCR1):c.82G>A (p.Gly28Ser)
NM_014053.4(FLVCR1):c.832T>C (p.Phe278Leu)
NM_014053.4(FLVCR1):c.877G>A (p.Ala293Thr)
NM_014053.4(FLVCR1):c.884-12G>A
NM_014053.4(FLVCR1):c.884-20C>T
NM_014053.4(FLVCR1):c.889A>G (p.Lys297Glu)
NM_014053.4(FLVCR1):c.901C>T (p.Arg301Trp)
NM_014053.4(FLVCR1):c.906T>C (p.Tyr302=)
NM_014053.4(FLVCR1):c.908C>T (p.Pro303Leu)
NM_014053.4(FLVCR1):c.937G>A (p.Asp313Asn) rs139175550
NM_014053.4(FLVCR1):c.944C>G (p.Pro315Arg)
NM_014053.4(FLVCR1):c.944C>T (p.Pro315Leu)
NM_014053.4(FLVCR1):c.952G>A (p.Glu318Lys) rs41297444
NM_014053.4(FLVCR1):c.974T>G (p.Ile325Arg)
NM_014053.4(FLVCR1):c.981C>T (p.Asn327=) rs886045928
NM_014053.4(FLVCR1):c.991A>C (p.Asn331His)
NM_014053.4(FLVCR1):c.996T>C (p.Ile332=) rs755552497

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