ClinVar Miner

List of variants in gene ANKRD11 reported by Athena Diagnostics Inc

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Gene type:
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Total variants: 41
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HGVS dbSNP
NM_013275.6(ANKRD11):c.1020G>A (p.Thr340=)
NM_013275.6(ANKRD11):c.1296G>C (p.Thr432=) rs74033734
NM_013275.6(ANKRD11):c.136G>A (p.Asp46Asn)
NM_013275.6(ANKRD11):c.149A>T (p.Glu50Val) rs1567614253
NM_013275.6(ANKRD11):c.1844C>G (p.Ala615Gly)
NM_013275.6(ANKRD11):c.1994A>G (p.Lys665Arg)
NM_013275.6(ANKRD11):c.2039C>G (p.Thr680Ser)
NM_013275.6(ANKRD11):c.2519G>A (p.Arg840Gln)
NM_013275.6(ANKRD11):c.3045C>G (p.Pro1015=)
NM_013275.6(ANKRD11):c.306G>C (p.Leu102=)
NM_013275.6(ANKRD11):c.3162A>G (p.Lys1054=) rs61729371
NM_013275.6(ANKRD11):c.3343A>G (p.Ile1115Val)
NM_013275.6(ANKRD11):c.3573C>G (p.Ala1191=) rs62000377
NM_013275.6(ANKRD11):c.3660G>A (p.Arg1220=)
NM_013275.6(ANKRD11):c.372G>A (p.Thr124=)
NM_013275.6(ANKRD11):c.375C>T (p.Ala125=)
NM_013275.6(ANKRD11):c.3822C>T (p.Ala1274=) rs61741725
NM_013275.6(ANKRD11):c.4344T>C (p.Tyr1448=)
NM_013275.6(ANKRD11):c.4872G>A (p.Ala1624=) rs143426579
NM_013275.6(ANKRD11):c.4932G>A (p.Gly1644=) rs72821356
NM_013275.6(ANKRD11):c.5088C>G (p.Asp1696Glu) rs146205997
NM_013275.6(ANKRD11):c.5198C>T (p.Ala1733Val) rs148243995
NM_013275.6(ANKRD11):c.5250C>T (p.Thr1750=)
NM_013275.6(ANKRD11):c.5338G>A (p.Ala1780Thr) rs75362060
NM_013275.6(ANKRD11):c.5629C>T (p.Pro1877Ser)
NM_013275.6(ANKRD11):c.5738C>A (p.Thr1913Asn)
NM_013275.6(ANKRD11):c.6046C>T (p.Pro2016Ser) rs1449729767
NM_013275.6(ANKRD11):c.6067G>C (p.Ala2023Pro) rs60520302
NM_013275.6(ANKRD11):c.6084C>T (p.Pro2028=)
NM_013275.6(ANKRD11):c.6140C>G (p.Ala2047Gly)
NM_013275.6(ANKRD11):c.6377G>A (p.Gly2126Asp)
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)
NM_013275.6(ANKRD11):c.6621C>T (p.Pro2207=)
NM_013275.6(ANKRD11):c.6704C>T (p.Pro2235Leu) rs1394383095
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly)
NM_013275.6(ANKRD11):c.6725C>T (p.Ala2242Val)
NM_013275.6(ANKRD11):c.6746G>A (p.Arg2249His)
NM_013275.6(ANKRD11):c.6787C>T (p.Pro2263Ser) rs76793093
NM_013275.6(ANKRD11):c.6792C>T (p.Pro2264=)
NM_013275.6(ANKRD11):c.6810C>T (p.Ala2270=) rs1210625952
NM_013275.6(ANKRD11):c.6919C>T (p.Pro2307Ser) rs575642464

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