ClinVar Miner

List of variants in gene F11 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.*296G>C rs4253430 0.39509
NM_000128.4(F11):c.1481-188C>T rs2289252 0.35266
NM_000128.4(F11):c.1191T>C (p.Gly397=) rs5970 0.16228
NM_000128.4(F11):c.801A>G (p.Thr267=) rs5974 0.16101
NM_000128.4(F11):c.1812G>T (p.Arg604=) rs5971 0.06917
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.1707C>T (p.Asp569=) rs5975 0.02893
NM_000128.4(F11):c.-54G>A rs4253814 0.01170
NM_000128.4(F11):c.1016G>T (p.Cys339Phe) rs5967 0.00559
NM_000128.4(F11):c.731A>G (p.Gln244Arg) rs5969 0.00538
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.218+20C>T rs11940999 0.00178
NM_000128.4(F11):c.1305-9G>T rs4253426 0.00153
NM_000128.4(F11):c.1599G>A (p.Gln533=) rs4253861 0.00115
NM_000128.4(F11):c.663C>T (p.Pro221=) rs142846329 0.00110
NM_000128.4(F11):c.1020C>T (p.Asn340=) rs149052026 0.00093
NM_000128.4(F11):c.539A>G (p.Lys180Arg) rs190283743 0.00036
NM_000128.4(F11):c.1577-11del rs776438459
NM_000128.4(F11):c.1577-11dup rs776438459
NM_000128.4(F11):c.219-11dup rs1483932983
NM_000128.4(F11):c.219-4dup rs573796016

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