ClinVar Miner

List of variants in gene F11 reported as benign for not provided

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.1136-309A>G rs4253421 0.90420
NM_000128.4(F11):c.56-282T>C rs2036914 0.57625
NM_000128.4(F11):c.*479A>T rs1062547 0.40400
NM_000128.4(F11):c.1577-297T>C rs73031655 0.40085
NM_000128.4(F11):c.756-165A>G rs2241817 0.40045
NM_000128.4(F11):c.*296G>C rs4253430 0.39990
NM_000128.4(F11):c.1481-188C>T rs2289252 0.35375
NM_000128.4(F11):c.1716+248G>A rs4253427 0.33169
NM_000128.4(F11):c.-1-196T>G rs4253399 0.30186
NM_000128.4(F11):c.-1-229T>C rs4253398 0.21890
NM_000128.3(F11):c.-316C>G rs3733403 0.18163
NM_000128.4(F11):c.*265A>G rs4253429 0.16938
NM_000128.4(F11):c.1136-244C>G rs4253422 0.16877
NM_000128.4(F11):c.1136-213A>G rs4253423 0.16698
NM_000128.4(F11):c.*852G>A rs4253431 0.16273
NM_000128.4(F11):c.1191T>C (p.Gly397=) rs5970 0.16228
NM_000128.4(F11):c.801A>G (p.Thr267=) rs5974 0.16187
NM_000128.4(F11):c.1577-148A>T rs138207591 0.14666
NM_000128.4(F11):c.*322G>A rs4253865 0.07317
NM_000128.4(F11):c.1481-215C>T rs2289251 0.06962
NM_000128.4(F11):c.1812G>T (p.Arg604=) rs5971 0.06917
NM_000128.4(F11):c.1717-48A>G rs5966 0.06916
NM_000128.4(F11):c.485+181T>C rs4253410 0.06528
NM_000128.4(F11):c.429C>T (p.Asp143=) rs5973 0.06445
NM_000128.4(F11):c.1839G>A (p.Glu613=) rs5976 0.04596
NM_000128.4(F11):c.326-120C>T rs4253837 0.03478
NM_000128.4(F11):c.755+216A>G rs554713191 0.03321
NM_000128.4(F11):c.1707C>T (p.Asp569=) rs5975 0.02893
NM_000128.4(F11):c.56-85T>C rs4253833 0.02454
NM_000128.4(F11):c.486-181C>T rs4253840 0.02171
NM_000128.4(F11):c.756-323C>G rs4253845 0.02158
NM_000128.4(F11):c.1716+168G>A rs184532749 0.02104
NM_000128.4(F11):c.-54G>A rs4253814 0.01170
NM_000128.4(F11):c.1016G>T (p.Cys339Phe) rs5967 0.00586
NM_000128.4(F11):c.731A>G (p.Gln244Arg) rs5969 0.00564
NM_000128.4(F11):c.*1A>G rs143899287 0.00378
NM_000128.4(F11):c.1304+12G>A rs116667976 0.00295
NM_000128.4(F11):c.453C>T (p.Tyr151=) rs34807019 0.00248
NM_000128.4(F11):c.1305-9G>T rs4253426 0.00153
NM_000128.4(F11):c.663C>T (p.Pro221=) rs142846329 0.00120
NM_000128.4(F11):c.1599G>A (p.Gln533=) rs4253861 0.00115
NM_000128.4(F11):c.1020C>T (p.Asn340=) rs149052026 0.00100
NM_000128.4(F11):c.539A>G (p.Lys180Arg) rs190283743 0.00036
NM_000128.4(F11):c.-1-138A>C rs3822057
NM_000128.4(F11):c.-1-148_-1-147insTA rs3841991
NM_000128.4(F11):c.1135+295_1135+296del rs33985758
NM_000128.4(F11):c.1135+296del rs33985758
NM_000128.4(F11):c.1481-34G>T rs2289253
NM_000128.4(F11):c.1576+51C>A rs2289254
NM_000128.4(F11):c.1577-11del
NM_000128.4(F11):c.1577-11dup
NM_000128.4(F11):c.1577-92AT[10] rs377566180
NM_000128.4(F11):c.1577-92AT[11] rs377566180
NM_000128.4(F11):c.1577-92AT[8] rs377566180
NM_000128.4(F11):c.1577-93_1577-92dup rs143389832
NM_000128.4(F11):c.1716+250G>A rs4253428
NM_000128.4(F11):c.218+20C>T
NM_000128.4(F11):c.219-11dup
NM_000128.4(F11):c.219-4dup
NM_000128.4(F11):c.485+122T>A rs1593
NM_000128.4(F11):c.486-280dup rs112655971
NM_000128.4(F11):c.755+213_755+214del rs33965536
NM_000128.4(F11):c.755+214del rs33965536

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