ClinVar Miner

List of variants in gene FLVCR1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_014053.4(FLVCR1):c.1631C>T (p.Thr544Met) rs3207090 0.38895
NM_014053.4(FLVCR1):c.*2860C>A rs138737189 0.00702
NM_014053.4(FLVCR1):c.-87G>A rs41296692 0.00410
NM_014053.4(FLVCR1):c.*166G>A rs41301017 0.00347
NM_014053.4(FLVCR1):c.937G>A (p.Asp313Asn) rs139175550 0.00251
NM_014053.4(FLVCR1):c.952G>A (p.Glu318Lys) rs41297444 0.00210
NM_014053.4(FLVCR1):c.738+9T>C rs41296696 0.00133
NM_014053.4(FLVCR1):c.1624C>T (p.Pro542Ser) rs141575859 0.00117
NM_014053.4(FLVCR1):c.*1300A>G rs186133334 0.00096
NM_014053.4(FLVCR1):c.*284G>A rs41301021 0.00080
NM_014053.4(FLVCR1):c.1657T>G (p.Ser553Ala) rs149887215 0.00064
NM_014053.4(FLVCR1):c.40C>T (p.Pro14Ser) rs111734301 0.00027
NM_014053.4(FLVCR1):c.663C>T (p.Pro221=) rs140209609 0.00019
NM_014053.4(FLVCR1):c.366C>T (p.Ala122=) rs374820446 0.00016
NM_014053.4(FLVCR1):c.1594-16_1594-15insCGAT rs146462077 0.00014
NM_014053.4(FLVCR1):c.*2887C>T rs186854246 0.00011
NM_014053.4(FLVCR1):c.1525+12C>T rs372644357 0.00011
NM_014053.4(FLVCR1):c.1196+14A>C rs776567536 0.00009
NM_014053.4(FLVCR1):c.738+16G>A rs371954696 0.00009
NM_014053.4(FLVCR1):c.525C>T (p.Leu175=) rs755329362 0.00008
NM_014053.4(FLVCR1):c.768A>G (p.Pro256=) rs774690148 0.00008
NM_014053.4(FLVCR1):c.1525+13G>A rs377087497 0.00005
NM_014053.4(FLVCR1):c.1093-16C>T rs759049446 0.00004
NM_014053.4(FLVCR1):c.1263C>T (p.Asp421=) rs762509082 0.00004
NM_014053.4(FLVCR1):c.1365C>T (p.Tyr455=) rs779980010 0.00004
NM_014053.4(FLVCR1):c.1525+17G>A rs903855418 0.00004
NM_014053.4(FLVCR1):c.884-20C>A rs1184401859 0.00004
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=) rs150645228 0.00003
NM_014053.4(FLVCR1):c.42C>T (p.Pro14=) rs886045923 0.00003
NM_014053.4(FLVCR1):c.532C>T (p.Leu178=) rs779152197 0.00003
NM_014053.4(FLVCR1):c.543C>T (p.Ser181=) rs753192864 0.00003
NM_014053.4(FLVCR1):c.1059G>A (p.Thr353=) rs550517136 0.00002
NM_014053.4(FLVCR1):c.738+10G>A rs771651161 0.00002
NM_014053.4(FLVCR1):c.996T>C (p.Ile332=) rs755552497 0.00002
NM_014053.4(FLVCR1):c.1017C>T (p.Ile339=) rs779552215 0.00001
NM_014053.4(FLVCR1):c.1063T>C (p.Leu355=) rs1312063756 0.00001
NM_014053.4(FLVCR1):c.1128G>A (p.Thr376=) rs780568170 0.00001
NM_014053.4(FLVCR1):c.1197-4T>G rs758496276 0.00001
NM_014053.4(FLVCR1):c.1258T>C (p.Leu420=) rs768084708 0.00001
NM_014053.4(FLVCR1):c.1284G>A (p.Val428=) rs373495747 0.00001
NM_014053.4(FLVCR1):c.1307+14G>T rs747174876 0.00001
NM_014053.4(FLVCR1):c.1359C>T (p.Ile453=) rs1314494158 0.00001
NM_014053.4(FLVCR1):c.1419T>C (p.Phe473=) rs1436451200 0.00001
NM_014053.4(FLVCR1):c.1521A>G (p.Leu507=) rs74607124 0.00001
NM_014053.4(FLVCR1):c.1528T>C (p.Leu510=) rs758323391 0.00001
NM_014053.4(FLVCR1):c.1594-10G>T rs1241817401 0.00001
NM_014053.4(FLVCR1):c.15C>T (p.Asp5=) rs1440383588 0.00001
NM_014053.4(FLVCR1):c.1626A>G (p.Pro542=) rs888869006 0.00001
NM_014053.4(FLVCR1):c.294G>T (p.Leu98=) rs376377158 0.00001
NM_014053.4(FLVCR1):c.306G>T (p.Ala102=) rs1164572739 0.00001
NM_014053.4(FLVCR1):c.312C>T (p.Ser104=) rs1169047994 0.00001
NM_014053.4(FLVCR1):c.501G>A (p.Leu167=) rs886043715 0.00001
NM_014053.4(FLVCR1):c.600C>T (p.Phe200=) rs761356341 0.00001
NM_014053.4(FLVCR1):c.666C>T (p.Ser222=) rs764566523 0.00001
NM_014053.4(FLVCR1):c.6G>A (p.Ala2=) rs1212330581 0.00001
NM_014053.4(FLVCR1):c.738+8C>T rs774389293 0.00001
NM_014053.4(FLVCR1):c.884-16T>C rs1164883996 0.00001
NM_014053.4(FLVCR1):c.981C>T (p.Asn327=) rs886045928 0.00001
NM_014053.4(FLVCR1):c.9G>C (p.Arg3=) rs1264346150 0.00001
NM_014053.3(FLVCR1):c.*4085_*4086delTT rs148146820
NM_014053.4(FLVCR1):c.*2061CA[13] rs139242973
NM_014053.4(FLVCR1):c.1023T>C (p.Tyr341=)
NM_014053.4(FLVCR1):c.1024+19C>T rs375807663
NM_014053.4(FLVCR1):c.1025-11_1025-8del
NM_014053.4(FLVCR1):c.1025-20A>G
NM_014053.4(FLVCR1):c.1025-20A>T rs369868359
NM_014053.4(FLVCR1):c.1092+11_1092+16del rs2102563658
NM_014053.4(FLVCR1):c.1092+12C>T
NM_014053.4(FLVCR1):c.1168T>C (p.Leu390=) rs2102565678
NM_014053.4(FLVCR1):c.1191A>C (p.Thr397=) rs140955508
NM_014053.4(FLVCR1):c.1191A>T (p.Thr397=)
NM_014053.4(FLVCR1):c.1194C>T (p.Tyr398=) rs1308191949
NM_014053.4(FLVCR1):c.1196+11_1196+15del
NM_014053.4(FLVCR1):c.1196+20T>C
NM_014053.4(FLVCR1):c.1197-17dup rs764296612
NM_014053.4(FLVCR1):c.1215T>G (p.Val405=)
NM_014053.4(FLVCR1):c.1281C>T (p.Ile427=) rs1016356701
NM_014053.4(FLVCR1):c.1414-11T>C rs184101744
NM_014053.4(FLVCR1):c.1431C>T (p.Phe477=)
NM_014053.4(FLVCR1):c.1467T>C (p.Gly489=) rs2102570244
NM_014053.4(FLVCR1):c.1506T>C (p.Phe502=)
NM_014053.4(FLVCR1):c.1525+11G>A
NM_014053.4(FLVCR1):c.1525+20T>G rs1558121111
NM_014053.4(FLVCR1):c.1584T>C (p.Asp528=)
NM_014053.4(FLVCR1):c.1593+20T>C
NM_014053.4(FLVCR1):c.1593+21del
NM_014053.4(FLVCR1):c.1594-10_1594-9insACTG rs762129441
NM_014053.4(FLVCR1):c.1594-16C>T
NM_014053.4(FLVCR1):c.1617C>T (p.Asp539=) rs1216578592
NM_014053.4(FLVCR1):c.1632G>A (p.Thr544=) rs751409998
NM_014053.4(FLVCR1):c.1632G>T (p.Thr544=) rs751409998
NM_014053.4(FLVCR1):c.1653A>G (p.Ser551=)
NM_014053.4(FLVCR1):c.18T>C (p.Asp6=)
NM_014053.4(FLVCR1):c.279C>A (p.Ala93=) rs765148657
NM_014053.4(FLVCR1):c.279C>T (p.Ala93=) rs765148657
NM_014053.4(FLVCR1):c.291G>T (p.Pro97=) rs757889545
NM_014053.4(FLVCR1):c.292C>T (p.Leu98=)
NM_014053.4(FLVCR1):c.303G>C (p.Thr101=) rs1189185318
NM_014053.4(FLVCR1):c.306G>A (p.Ala102=) rs1164572739
NM_014053.4(FLVCR1):c.327G>C (p.Val109=)
NM_014053.4(FLVCR1):c.354G>A (p.Ser118=)
NM_014053.4(FLVCR1):c.354G>C (p.Ser118=) rs752628417
NM_014053.4(FLVCR1):c.354G>T (p.Ser118=)
NM_014053.4(FLVCR1):c.360C>T (p.Val120=)
NM_014053.4(FLVCR1):c.372G>A (p.Gln124=) rs1251461956
NM_014053.4(FLVCR1):c.378C>T (p.Ile126=) rs2102526976
NM_014053.4(FLVCR1):c.405C>T (p.Phe135=)
NM_014053.4(FLVCR1):c.447G>A (p.Leu149=)
NM_014053.4(FLVCR1):c.480C>T (p.Leu160=) rs1398426157
NM_014053.4(FLVCR1):c.561T>G (p.Gly187=)
NM_014053.4(FLVCR1):c.579C>T (p.Gly193=)
NM_014053.4(FLVCR1):c.591G>A (p.Gln197=)
NM_014053.4(FLVCR1):c.594T>C (p.His198=)
NM_014053.4(FLVCR1):c.630C>T (p.Cys210=)
NM_014053.4(FLVCR1):c.675C>G (p.Ala225=)
NM_014053.4(FLVCR1):c.690G>A (p.Gly230=) rs1352757781
NM_014053.4(FLVCR1):c.717C>T (p.Ala239=)
NM_014053.4(FLVCR1):c.739-13A>G
NM_014053.4(FLVCR1):c.750A>T (p.Ala250=)
NM_014053.4(FLVCR1):c.789A>G (p.Thr263=)
NM_014053.4(FLVCR1):c.834T>C (p.Phe278=)
NM_014053.4(FLVCR1):c.884-15C>T
NM_014053.4(FLVCR1):c.884-20C>T rs1184401859
NM_014053.4(FLVCR1):c.884-8A>G
NM_014053.4(FLVCR1):c.906T>C (p.Tyr302=) rs2102551378
NM_014053.4(FLVCR1):c.984G>A (p.Leu328=)

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