ClinVar Miner

List of variants in gene RAX2 reported as likely benign for not provided

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Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_001319074.4(RAX2):c.216+72C>T rs140251615 0.00625
NM_001319074.4(RAX2):c.45T>G (p.Gly15=) rs139127905 0.00435
NM_001319074.4(RAX2):c.-331C>T rs150444854 0.00389
NM_001319074.4(RAX2):c.*45C>T rs139146360 0.00120
NM_001319074.4(RAX2):c.*191C>T rs150808899 0.00099
NM_001319074.4(RAX2):c.156G>A (p.Pro52=) rs141804618 0.00059
NM_001319074.4(RAX2):c.-281G>A rs182965071 0.00048
NM_001319074.4(RAX2):c.33C>T (p.Thr11=) rs149515429 0.00038
NM_001319074.4(RAX2):c.*1169G>A rs554924169 0.00031
NM_001319074.4(RAX2):c.216+16A>G rs368777860 0.00021
NM_001319074.4(RAX2):c.186C>A (p.Ala62=) rs775483414 0.00010
NM_001319074.4(RAX2):c.294G>A (p.Pro98=) rs191051622 0.00007
NM_001319074.4(RAX2):c.12C>G (p.Ser4Arg) rs201416315 0.00004
NM_001319074.4(RAX2):c.27G>A (p.Pro9=) rs764316452 0.00004
NM_001319074.4(RAX2):c.324C>T (p.Phe108=) rs749859588 0.00004
NM_001319074.4(RAX2):c.510C>T (p.Ala170=) rs941485794 0.00004
NM_001319074.4(RAX2):c.54G>A (p.Pro18=) rs367658021 0.00004
NM_001319074.4(RAX2):c.195C>T (p.His65=) rs1252557730 0.00003
NM_001319074.4(RAX2):c.500G>A (p.Arg167Gln) rs202103390 0.00003
NM_001319074.4(RAX2):c.138C>T (p.Phe46=) rs771416905 0.00002
NM_001319074.4(RAX2):c.235C>A (p.Arg79=) rs1294461966 0.00002
NM_001319074.4(RAX2):c.276G>A (p.Ser92=) rs751453416 0.00002
NM_001319074.4(RAX2):c.321G>A (p.Pro107=) rs771534203 0.00002
NM_001319074.4(RAX2):c.465C>T (p.Phe155=) rs923302208 0.00002
NM_001319074.4(RAX2):c.552C>T (p.Ala184=) rs1291600031 0.00002
NM_001319074.4(RAX2):c.135G>A (p.Ala45=) rs1163670829 0.00001
NM_001319074.4(RAX2):c.15G>A (p.Pro5=) rs781275318 0.00001
NM_001319074.4(RAX2):c.18C>T (p.Gly6=) rs755028810 0.00001
NM_001319074.4(RAX2):c.216+9A>G rs747374602 0.00001
NM_001319074.4(RAX2):c.217-10C>T rs772762463 0.00001
NM_001319074.4(RAX2):c.217-16C>G rs1321549398 0.00001
NM_001319074.4(RAX2):c.309C>T (p.Ala103=) rs1463116025 0.00001
NM_001319074.4(RAX2):c.336G>A (p.Pro112=) rs1568400696 0.00001
NM_001319074.4(RAX2):c.381G>A (p.Pro127=) rs895500531 0.00001
NM_001319074.4(RAX2):c.411C>T (p.Gly137=) rs1248541458 0.00001
NM_001319074.4(RAX2):c.414G>A (p.Pro138=) rs1335212510 0.00001
NM_001319074.4(RAX2):c.420G>A (p.Pro140=) rs947549671 0.00001
NM_001319074.4(RAX2):c.444T>C (p.Pro148=) rs1439994082 0.00001
NM_001319074.4(RAX2):c.459C>T (p.Pro153=) rs1486188826 0.00001
NM_001319074.4(RAX2):c.477C>T (p.Phe159=) rs763649255 0.00001
NM_001319074.4(RAX2):c.57C>T (p.Gly19=) rs769403788 0.00001
NM_001319074.4(RAX2):c.126G>A (p.Leu42=) rs2145737312
NM_001319074.4(RAX2):c.147T>C (p.Ser49=)
NM_001319074.4(RAX2):c.156G>C (p.Pro52=)
NM_001319074.4(RAX2):c.165C>T (p.Tyr55=)
NM_001319074.4(RAX2):c.177G>A (p.Glu59=)
NM_001319074.4(RAX2):c.18C>A (p.Gly6=)
NM_001319074.4(RAX2):c.207G>A (p.Val69=) rs773887682
NM_001319074.4(RAX2):c.210C>G (p.Arg70=)
NM_001319074.4(RAX2):c.216+11C>T rs758919828
NM_001319074.4(RAX2):c.216+20C>T
NM_001319074.4(RAX2):c.216+6_216+7insCA
NM_001319074.4(RAX2):c.217-11G>A
NM_001319074.4(RAX2):c.217-12C>T rs530784939
NM_001319074.4(RAX2):c.217-4C>T
NM_001319074.4(RAX2):c.217-7C>T
NM_001319074.4(RAX2):c.217-8C>A rs79588413
NM_001319074.4(RAX2):c.234C>G (p.Arg78=)
NM_001319074.4(RAX2):c.243G>A (p.Lys81=) rs757897383
NM_001319074.4(RAX2):c.24G>T (p.Gly8=)
NM_001319074.4(RAX2):c.252C>A (p.Arg84=) rs2037250863
NM_001319074.4(RAX2):c.276G>C (p.Ser92=)
NM_001319074.4(RAX2):c.285G>A (p.Val95=)
NM_001319074.4(RAX2):c.300C>A (p.Leu100=) rs2145736395
NM_001319074.4(RAX2):c.303C>T (p.Pro101=)
NM_001319074.4(RAX2):c.315G>A (p.Ala105=)
NM_001319074.4(RAX2):c.330C>T (p.Arg110=) rs2037248782
NM_001319074.4(RAX2):c.369C>T (p.Gly123=)
NM_001319074.4(RAX2):c.378G>A (p.Pro126=)
NM_001319074.4(RAX2):c.387G>A (p.Val129=)
NM_001319074.4(RAX2):c.399C>T (p.Pro133=)
NM_001319074.4(RAX2):c.411CCCGGG[3] (p.138PG[3]) rs549932754
NM_001319074.4(RAX2):c.417C>T (p.Gly139=)
NM_001319074.4(RAX2):c.426G>A (p.Leu142=)
NM_001319074.4(RAX2):c.438C>T (p.Phe146=)
NM_001319074.4(RAX2):c.45T>C (p.Gly15=)
NM_001319074.4(RAX2):c.546G>A (p.Pro182=)
NM_001319074.4(RAX2):c.66C>T (p.Ala22=)
NM_001319074.4(RAX2):c.69C>T (p.Pro23=) rs1568401195
NM_001319074.4(RAX2):c.90C>T (p.Asn30=)

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