ClinVar Miner

List of variants in gene F11 reported as uncertain significance by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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NM_000128.3(F11):c.1028+9T>C rs376630194
NM_000128.3(F11):c.1200G>A (p.Pro400=) rs150377265
NM_000128.3(F11):c.1431C>T (p.Ser477=) rs149568223
NM_000128.4(F11):c.1001C>T (p.Pro334Leu)
NM_000128.4(F11):c.1011A>G (p.Ala337=)
NM_000128.4(F11):c.1059C>T (p.Asn353=)
NM_000128.4(F11):c.1174A>G (p.Thr392Ala)
NM_000128.4(F11):c.1579A>G (p.Lys527Glu)
NM_000128.4(F11):c.1609A>T (p.Ile537Leu)
NM_000128.4(F11):c.1625A>G (p.Asn542Ser)
NM_000128.4(F11):c.1683C>T (p.Ala561=)
NM_000128.4(F11):c.1709C>G (p.Ala570Gly)
NM_000128.4(F11):c.1767G>T (p.Leu589=)
NM_000128.4(F11):c.291G>A (p.Gly97=)
NM_000128.4(F11):c.486-10T>A rs370991682
NM_000128.4(F11):c.536C>T (p.Thr179Met)
NM_000128.4(F11):c.596-6G>A rs369721182
NM_000128.4(F11):c.696T>C (p.His232=) rs746382259
NM_000128.4(F11):c.852G>C (p.Arg284Ser)

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