ClinVar Miner

List of variants in gene ANKRD11 reported as benign by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_013275.6(ANKRD11):c.1020G>A (p.Thr340=) rs142539117
NM_013275.6(ANKRD11):c.1296G>C (p.Thr432=) rs74033734
NM_013275.6(ANKRD11):c.1844C>G (p.Ala615Gly) rs115797011
NM_013275.6(ANKRD11):c.2039C>G (p.Thr680Ser) rs145694621
NM_013275.6(ANKRD11):c.2519G>A (p.Arg840Gln) rs149776253
NM_013275.6(ANKRD11):c.3045C>G (p.Pro1015=) rs150652124
NM_013275.6(ANKRD11):c.306G>C (p.Leu102=) rs150497848
NM_013275.6(ANKRD11):c.3162A>G (p.Lys1054=) rs61729371
NM_013275.6(ANKRD11):c.3573C>G (p.Ala1191=) rs62000377
NM_013275.6(ANKRD11):c.3660G>A (p.Arg1220=) rs150015583
NM_013275.6(ANKRD11):c.372G>A (p.Thr124=) rs34016116
NM_013275.6(ANKRD11):c.3822C>T (p.Ala1274=) rs61741725
NM_013275.6(ANKRD11):c.4344T>C (p.Tyr1448=) rs61744778
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=) rs202126162
NM_013275.6(ANKRD11):c.5338G>A (p.Ala1780Thr) rs75362060
NM_013275.6(ANKRD11):c.5413G>A (p.Val1805Ile) rs151288302
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser) rs145906515
NM_013275.6(ANKRD11):c.5738C>A (p.Thr1913Asn) rs142373563
NM_013275.6(ANKRD11):c.6067G>C (p.Ala2023Pro) rs60520302
NM_013275.6(ANKRD11):c.6084C>T (p.Pro2028=) rs189297725
NM_013275.6(ANKRD11):c.6597C>G (p.Leu2199=) rs762643863
NM_013275.6(ANKRD11):c.6725C>T (p.Ala2242Val) rs372632879
NM_013275.6(ANKRD11):c.6730G>A (p.Val2244Ile) rs200852197
NM_013275.6(ANKRD11):c.6746G>A (p.Arg2249His) rs201043388
NM_013275.6(ANKRD11):c.6787C>T (p.Pro2263Ser) rs76793093
NM_013275.6(ANKRD11):c.6826C>T (p.Pro2276Ser) rs201957371
NM_013275.6(ANKRD11):c.6977C>G (p.Ala2326Gly) rs576742682

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