ClinVar Miner

List of variants in gene FLVCR1 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_014053.4(FLVCR1):c.*1106C>T rs12567728
NM_014053.4(FLVCR1):c.*1151A>G rs6682947
NM_014053.4(FLVCR1):c.*1317A>G rs145011972
NM_014053.4(FLVCR1):c.*1544A>G rs6685793
NM_014053.4(FLVCR1):c.*1600G>A rs55793082
NM_014053.4(FLVCR1):c.*1609A>G rs12405742
NM_014053.4(FLVCR1):c.*1751C>T rs187971996
NM_014053.4(FLVCR1):c.*1793C>T rs12567975
NM_014053.4(FLVCR1):c.*1826C>T rs12567976
NM_014053.4(FLVCR1):c.*1880_*1883TAAA[7] rs141272551
NM_014053.4(FLVCR1):c.*1920T>A
NM_014053.4(FLVCR1):c.*1940G>A rs6697126
NM_014053.4(FLVCR1):c.*2061_*2062CA[12] rs139242973
NM_014053.4(FLVCR1):c.*2419G>A rs10864027
NM_014053.4(FLVCR1):c.*2443C>T rs117380165
NM_014053.4(FLVCR1):c.*2540T>C
NM_014053.4(FLVCR1):c.*2578G>A rs1284856
NM_014053.4(FLVCR1):c.*2709T>C rs1284855
NM_014053.4(FLVCR1):c.*279T>C rs17019875
NM_014053.4(FLVCR1):c.*2813G>A rs1284854
NM_014053.4(FLVCR1):c.*2908G>A rs1284853
NM_014053.4(FLVCR1):c.*2968G>A rs10902
NM_014053.4(FLVCR1):c.*3032G>T
NM_014053.4(FLVCR1):c.*3130_*3131insAATT rs10655434
NM_014053.4(FLVCR1):c.*3241C>T rs113198161
NM_014053.4(FLVCR1):c.*3264T>C rs374214375
NM_014053.4(FLVCR1):c.*3313G>T rs15903
NM_014053.4(FLVCR1):c.*339T>G rs12074192
NM_014053.4(FLVCR1):c.*3482C>G rs12142813
NM_014053.4(FLVCR1):c.*353A>G rs6679775
NM_014053.4(FLVCR1):c.*377T>C rs41258034
NM_014053.4(FLVCR1):c.*500G>A
NM_014053.4(FLVCR1):c.*626T>A rs11582817
NM_014053.4(FLVCR1):c.*673G>A rs41301027
NM_014053.4(FLVCR1):c.*788C>T rs6670064
NM_014053.4(FLVCR1):c.*844T>C rs12565125
NM_014053.4(FLVCR1):c.*855T>C rs564661630
NM_014053.4(FLVCR1):c.*891A>G rs41301029
NM_014053.4(FLVCR1):c.*931C>T rs12567713
NM_014053.4(FLVCR1):c.-86C>T rs2201603
NM_014053.4(FLVCR1):c.1272T>C (p.Tyr424=) rs17677416
NM_014053.4(FLVCR1):c.154G>C (p.Ala52Pro) rs11120047
NM_014053.4(FLVCR1):c.1593+9T>C rs17019870
NM_014053.4(FLVCR1):c.1631C>T (p.Thr544Met) rs3207090
NM_014053.4(FLVCR1):c.937G>A (p.Asp313Asn) rs139175550

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