ClinVar Miner

List of variants in gene F11 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
NM_000128.3(F11):c.1028+9T>C rs376630194
NM_000128.3(F11):c.1200G>A (p.Pro400=) rs150377265
NM_000128.3(F11):c.1305-5C>T rs375998777
NM_000128.3(F11):c.1431C>T (p.Ser477=) rs149568223
NM_000128.4(F11):c.1008A>G (p.Gln336=) rs376999986
NM_000128.4(F11):c.1028+9T>G
NM_000128.4(F11):c.1056A>G (p.Ser352=)
NM_000128.4(F11):c.1059C>T (p.Asn353=)
NM_000128.4(F11):c.1083C>T (p.His361=)
NM_000128.4(F11):c.111G>A (p.Thr37=) rs762996950
NM_000128.4(F11):c.114C>T (p.Val38=)
NM_000128.4(F11):c.1158C>G (p.Pro386=)
NM_000128.4(F11):c.1179G>A (p.Ala393=)
NM_000128.4(F11):c.117C>T (p.Phe39=)
NM_000128.4(F11):c.1224C>T (p.Thr408=)
NM_000128.4(F11):c.1254C>G (p.Gly418=)
NM_000128.4(F11):c.1255T>A (p.Ser419Thr)
NM_000128.4(F11):c.126C>T (p.Ser42=) rs754973084
NM_000128.4(F11):c.1287C>A (p.Ala429=)
NM_000128.4(F11):c.1287C>T (p.Ala429=) rs138122638
NM_000128.4(F11):c.1305-10T>G
NM_000128.4(F11):c.1324T>C (p.Leu442=)
NM_000128.4(F11):c.132G>A (p.Lys44=)
NM_000128.4(F11):c.1518T>C (p.Asp506=)
NM_000128.4(F11):c.1519A>C (p.Arg507=)
NM_000128.4(F11):c.1521A>G (p.Arg507=)
NM_000128.4(F11):c.1525G>A (p.Val509Ile)
NM_000128.4(F11):c.1560G>A (p.Gly520=)
NM_000128.4(F11):c.159C>T (p.His53=)
NM_000128.4(F11):c.1626C>T (p.Asn542=)
NM_000128.4(F11):c.162A>G (p.Pro54=)
NM_000128.4(F11):c.1716+7G>A
NM_000128.4(F11):c.1717-7G>A rs778179698
NM_000128.4(F11):c.1717-8C>T
NM_000128.4(F11):c.1725G>A (p.Ser575=)
NM_000128.4(F11):c.1767G>T (p.Leu589=)
NM_000128.4(F11):c.1779G>A (p.Thr593=)
NM_000128.4(F11):c.1782C>T (p.Ser594=)
NM_000128.4(F11):c.1788C>T (p.Gly596=)
NM_000128.4(F11):c.1830C>T (p.Asn610=)
NM_000128.4(F11):c.1836C>T (p.Val612=)
NM_000128.4(F11):c.1842C>T (p.Tyr614=)
NM_000128.4(F11):c.1843G>A (p.Val615Met) rs202061241
NM_000128.4(F11):c.186G>C (p.Thr62=)
NM_000128.4(F11):c.189G>T (p.Ala63=)
NM_000128.4(F11):c.218+7G>A
NM_000128.4(F11):c.219-10A>T
NM_000128.4(F11):c.325+10G>A
NM_000128.4(F11):c.330C>T (p.Cys110=)
NM_000128.4(F11):c.450G>A (p.Thr150=)
NM_000128.4(F11):c.485+7G>A
NM_000128.4(F11):c.486-10T>A rs370991682
NM_000128.4(F11):c.507C>T (p.His169=) rs367559663
NM_000128.4(F11):c.537G>A (p.Thr179=)
NM_000128.4(F11):c.543C>T (p.Leu181=)
NM_000128.4(F11):c.56-6T>C
NM_000128.4(F11):c.595+10G>A
NM_000128.4(F11):c.596-10C>T
NM_000128.4(F11):c.596-5C>T
NM_000128.4(F11):c.596-6G>A rs369721182
NM_000128.4(F11):c.596-9G>A
NM_000128.4(F11):c.606G>A (p.Arg202=)
NM_000128.4(F11):c.642C>T (p.Asn214=)
NM_000128.4(F11):c.654C>A (p.Val218=)
NM_000128.4(F11):c.687C>T (p.Ile229=)
NM_000128.4(F11):c.696T>C (p.His232=) rs746382259
NM_000128.4(F11):c.755+10T>G
NM_000128.4(F11):c.756-5G>A
NM_000128.4(F11):c.797G>A (p.Ser266Asn) rs145168351
NM_000128.4(F11):c.840A>G (p.Leu280=)
NM_000128.4(F11):c.861C>T (p.Ile287=) rs5964
NM_000128.4(F11):c.866-8C>T
NM_000128.4(F11):c.866-9G>A rs200218867
NM_000128.4(F11):c.942C>T (p.His314=)
NM_000128.4(F11):c.948C>G (p.Ala316=)
NM_000128.4(F11):c.96A>C (p.Gly32=) rs368183250

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