ClinVar Miner

List of variants in gene FOXI1 reported as uncertain significance for autosomal recessive nonsyndromic hearing loss 4

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_012188.5(FOXI1):c.726C>T (p.Ser242=) rs35678180 0.00520
NM_012188.5(FOXI1):c.677C>T (p.Thr226Ile) rs115399307 0.00376
NM_012188.5(FOXI1):c.318C>G (p.Asp106Glu) rs114293092 0.00289
NM_012188.5(FOXI1):c.30C>T (p.Ser10=) rs137901435 0.00166
NM_012188.5(FOXI1):c.822C>T (p.Gly274=) rs149203108 0.00105
NM_012188.5(FOXI1):c.1018C>G (p.Pro340Ala) rs141924917 0.00082
NM_012188.5(FOXI1):c.442C>G (p.Gln148Glu) rs553561553 0.00077
NM_012188.5(FOXI1):c.*576T>A rs550861326 0.00054
NM_012188.5(FOXI1):c.825C>T (p.Ala275=) rs147596900 0.00054
NM_012188.5(FOXI1):c.*986G>C rs111876035 0.00053
NM_012188.5(FOXI1):c.727C>A (p.Pro243Thr) rs377539902 0.00050
NM_012188.5(FOXI1):c.997G>A (p.Gly333Ser) rs145046338 0.00034
NM_012188.5(FOXI1):c.1088G>T (p.Ser363Ile) rs150705492 0.00031
NM_012188.5(FOXI1):c.308G>C (p.Gly103Ala) rs370450076 0.00026
NM_012188.5(FOXI1):c.1090G>A (p.Val364Ile) rs201090454 0.00022
NM_012188.5(FOXI1):c.1013C>T (p.Ala338Val) rs367809742 0.00020
NM_012188.5(FOXI1):c.*679C>T rs966422889 0.00010
NM_012188.5(FOXI1):c.861C>G (p.Ala287=) rs145785746 0.00008
NM_012188.5(FOXI1):c.773G>A (p.Gly258Glu) rs121909340 0.00005
NM_012188.5(FOXI1):c.*418T>C rs886060402 0.00004
NM_012188.5(FOXI1):c.545A>G (p.Lys182Arg) rs772882906 0.00003
NM_012188.5(FOXI1):c.*74G>A rs1235816008 0.00002
NM_012188.5(FOXI1):c.937G>C (p.Gly313Arg) rs755810719 0.00002
NM_012188.5(FOXI1):c.*248G>A rs1758583401 0.00001
NM_012188.5(FOXI1):c.*397A>T rs886060401 0.00001
NM_012188.5(FOXI1):c.*486C>T rs886060403 0.00001
NM_012188.5(FOXI1):c.-18G>A rs764490860 0.00001
NM_012188.5(FOXI1):c.161A>G (p.Glu54Gly) rs1417785705 0.00001
NM_012188.5(FOXI1):c.63C>T (p.Ile21=) rs768858662 0.00001
NM_012188.5(FOXI1):c.763G>A (p.Ala255Thr) rs951259617 0.00001
NM_012188.5(FOXI1):c.*1094T>C rs1758609305
NM_012188.5(FOXI1):c.*176G>T rs151161274
NM_012188.5(FOXI1):c.*285A>G rs1758584609
NM_012188.5(FOXI1):c.*707C>T rs886060404
NM_012188.5(FOXI1):c.*815C>T rs550211890
NM_012188.5(FOXI1):c.*840G>T rs1758600627
NM_012188.5(FOXI1):c.1004G>A (p.Gly335Asp) rs764345848
NM_012188.5(FOXI1):c.269G>A (p.Gly90Glu) rs749433068
NM_012188.5(FOXI1):c.307G>T (p.Gly103Trp) rs1053809070
NM_012188.5(FOXI1):c.528G>A (p.Ser176=) rs373094576
NM_012188.5(FOXI1):c.568G>C (p.Asp190His) rs886060398
NM_012188.5(FOXI1):c.80A>C (p.Glu27Ala)
NM_012188.5(FOXI1):c.938G>A (p.Gly313Glu) rs886060399
NM_012188.5(FOXI1):c.972G>C (p.Pro324=) rs56128152

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