ClinVar Miner

List of variants in gene F11 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.*551A>T rs186377697 0.00654
NM_000128.4(F11):c.*404A>G rs139159299 0.00471
NM_000128.4(F11):c.1305-9G>T rs4253426 0.00153
NM_000128.4(F11):c.861C>T (p.Ile287=) rs5964 0.00107
NM_000128.4(F11):c.1020C>T (p.Asn340=) rs149052026 0.00100
NM_000128.4(F11):c.*822A>G rs558079340 0.00067
NM_000128.4(F11):c.*928G>A rs556465646 0.00043
NM_000128.4(F11):c.*728T>C rs566734345 0.00033
NM_000128.4(F11):c.*584A>T rs766777099 0.00024
NM_000128.4(F11):c.1029-11T>C rs373348576 0.00021
NM_000128.4(F11):c.1028+9T>C rs376630194 0.00020
NM_000128.4(F11):c.*952G>A rs886059303 0.00016
NM_000128.4(F11):c.1431C>T (p.Ser477=) rs149568223 0.00016
NM_000128.4(F11):c.596-6G>A rs369721182 0.00015
NM_000128.4(F11):c.*902G>A rs555668089 0.00010
NM_000128.4(F11):c.*346A>G rs1033944547 0.00009
NM_000128.4(F11):c.1305-14T>C rs199761451 0.00009
NM_000128.4(F11):c.1200G>A (p.Pro400=) rs150377265 0.00007
NM_000128.3(F11):c.-183T>C rs886059297 0.00006
NM_000128.4(F11):c.-57G>A rs1043431996 0.00006
NM_000128.4(F11):c.1480+4C>T rs370328133 0.00006
NM_000128.4(F11):c.1836C>T (p.Val612=) rs775708833 0.00006
NM_000128.4(F11):c.219-11T>A rs886059298 0.00006
NM_000128.4(F11):c.642C>T (p.Asn214=) rs372572261 0.00006
NM_000128.4(F11):c.*576G>A rs886059301 0.00005
NM_000128.4(F11):c.345T>C (p.Tyr115=) rs766137229 0.00004
NM_000128.4(F11):c.400C>T (p.Gln134Ter) rs756908183 0.00004
NM_000128.4(F11):c.56-6T>C rs374122923 0.00004
NM_000128.4(F11):c.478G>T (p.Glu160Ter) rs376961859 0.00003
NM_000128.4(F11):c.*1033A>G rs886059305 0.00002
NM_000128.4(F11):c.-70G>A rs755606015 0.00002
NM_000128.4(F11):c.1219A>G (p.Thr407Ala) rs369822221 0.00002
NM_000128.4(F11):c.1842C>T (p.Tyr614=) rs143588436 0.00002
NM_000128.4(F11):c.325G>A (p.Ala109Thr) rs768474112 0.00002
NM_000128.4(F11):c.696T>C (p.His232=) rs746382259 0.00002
NM_000128.3(F11):c.-326C>G rs753031984 0.00001
NM_000128.4(F11):c.*448A>G rs368132203 0.00001
NM_000128.4(F11):c.*763T>A rs576164426 0.00001
NM_000128.4(F11):c.*817A>G rs1441037997 0.00001
NM_000128.4(F11):c.*846T>C rs988525367 0.00001
NM_000128.4(F11):c.1416T>C (p.Tyr472=) rs1053472547 0.00001
NM_000128.4(F11):c.499C>T (p.Leu167=) rs374761594 0.00001
NM_000128.3(F11):c.-164G>A rs1739485056
NM_000128.3(F11):c.-233C>T rs1263431242
NM_000128.3(F11):c.-300C>T rs886059296
NM_000128.4(F11):c.*1039G>A rs1741449262
NM_000128.4(F11):c.*174C>T rs1741399736
NM_000128.4(F11):c.*262A>G rs886059300
NM_000128.4(F11):c.*445C>T rs1741414677
NM_000128.4(F11):c.*609C>A rs938214207
NM_000128.4(F11):c.*636A>G rs886059302
NM_000128.4(F11):c.*933C>G rs982607401
NM_000128.4(F11):c.*974ATT[1] rs886059304
NM_000128.4(F11):c.1325del (p.Leu442fs) rs757530565
NM_000128.4(F11):c.1481-1G>T rs1057516506
NM_000128.4(F11):c.1777A>G (p.Thr593Ala) rs1741382224

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