ClinVar Miner

List of variants in gene RBFOX3 reported as uncertain significance for EIG1

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_001082575.2(RBFOX3):c.118C>T (p.Pro40Ser)
NM_001082575.2(RBFOX3):c.166G>A (p.Glu56Lys) rs748110754
NM_001082575.2(RBFOX3):c.185C>T (p.Ala62Val)
NM_001082575.2(RBFOX3):c.19C>T (p.Pro7Ser) rs376060745
NM_001082575.2(RBFOX3):c.20C>T (p.Pro7Leu)
NM_001082575.2(RBFOX3):c.21C>A (p.Pro7=) rs751793355
NM_001082575.2(RBFOX3):c.222G>A (p.Pro74=)
NM_001082575.2(RBFOX3):c.232G>A (p.Glu78Lys) rs1032718998
NM_001082575.2(RBFOX3):c.245C>T (p.Thr82Met)
NM_001082575.2(RBFOX3):c.257C>T (p.Pro86Leu) rs377660420
NM_001082575.2(RBFOX3):c.273C>A (p.Asp91Glu) rs1599450000
NM_001082575.2(RBFOX3):c.347G>A (p.Arg116Gln) rs199891032
NM_001082575.2(RBFOX3):c.414G>C (p.Lys138Asn) rs1568134061
NM_001082575.2(RBFOX3):c.436G>C (p.Glu146Gln) rs1340183543
NM_001082575.2(RBFOX3):c.458G>A (p.Arg153Gln)
NM_001082575.2(RBFOX3):c.522G>A (p.Thr174=) rs776142495
NM_001082575.2(RBFOX3):c.54C>G (p.Ile18Met)
NM_001082575.2(RBFOX3):c.556C>A (p.Pro186Thr) rs372072435
NM_001082575.2(RBFOX3):c.568+6G>C rs953699995
NM_001082575.2(RBFOX3):c.62A>C (p.Glu21Ala) rs1167103679
NM_001082575.2(RBFOX3):c.646A>G (p.Thr216Ala)
NM_001082575.2(RBFOX3):c.673G>A (p.Ala225Thr) rs1479403018
NM_001082575.2(RBFOX3):c.679C>A (p.Leu227Ile) rs565220696
NM_001082575.2(RBFOX3):c.688C>T (p.Arg230Trp)
NM_001082575.2(RBFOX3):c.68C>T (p.Ala23Val) rs878854171
NM_001082575.2(RBFOX3):c.700G>A (p.Val234Met) rs921899416
NM_001082575.2(RBFOX3):c.709A>G (p.Thr237Ala)
NM_001082575.2(RBFOX3):c.714T>G (p.Phe238Leu) rs1599396290
NM_001082575.2(RBFOX3):c.718G>A (p.Ala240Thr)
NM_001082575.2(RBFOX3):c.71C>T (p.Pro24Leu)
NM_001082575.2(RBFOX3):c.80C>T (p.Pro27Leu)
NM_001082575.2(RBFOX3):c.858-9C>G
NM_001082575.2(RBFOX3):c.910G>A (p.Ala304Thr) rs1003593947
NM_001082575.2(RBFOX3):c.914C>T (p.Ala305Val) rs1294363374
NM_001082575.2(RBFOX3):c.936+6G>A rs757903881

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