ClinVar Miner

List of variants in gene RBFOX3 reported as uncertain significance for EIG

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_001082575.2(RBFOX3):c.166G>A (p.Glu56Lys)
NM_001082575.2(RBFOX3):c.19C>T (p.Pro7Ser) rs376060745
NM_001082575.2(RBFOX3):c.232G>A (p.Glu78Lys)
NM_001082575.2(RBFOX3):c.257C>T (p.Pro86Leu) rs377660420
NM_001082575.2(RBFOX3):c.271G>A (p.Asp91Asn) rs375940495
NM_001082575.2(RBFOX3):c.347G>A (p.Arg116Gln) rs199891032
NM_001082575.2(RBFOX3):c.414G>C (p.Lys138Asn)
NM_001082575.2(RBFOX3):c.548C>T (p.Thr183Met) rs542684395
NM_001082575.2(RBFOX3):c.556C>A (p.Pro186Thr) rs372072435
NM_001082575.2(RBFOX3):c.568+6G>C
NM_001082575.2(RBFOX3):c.62A>C (p.Glu21Ala) rs1167103679
NM_001082575.2(RBFOX3):c.68C>T (p.Ala23Val) rs878854171
NM_001082575.2(RBFOX3):c.914C>T (p.Ala305Val) rs1294363374

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