ClinVar Miner

List of variants in gene ANKRD11 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.301G>A (p.Gly101Arg) rs1373571533 0.00002
NM_013275.6(ANKRD11):c.3340T>A (p.Tyr1114Asn) rs1461435321 0.00001
NM_013275.6(ANKRD11):c.6127G>A (p.Ala2043Thr) rs1322632964 0.00001
NM_013275.6(ANKRD11):c.7531G>A (p.Val2511Ile) rs777571791 0.00001
NM_013275.6(ANKRD11):c.-2C>T
NM_013275.6(ANKRD11):c.1060_1089del (p.Glu354_Asp363del)
NM_013275.6(ANKRD11):c.1136G>C (p.Ser379Thr)
NM_013275.6(ANKRD11):c.1187C>T (p.Thr396Met) rs145699896
NM_013275.6(ANKRD11):c.118C>T (p.Pro40Ser) rs1597551527
NM_013275.6(ANKRD11):c.1354A>G (p.Asn452Asp)
NM_013275.6(ANKRD11):c.2014A>G (p.Ile672Val)
NM_013275.6(ANKRD11):c.2071C>T (p.Arg691Cys)
NM_013275.6(ANKRD11):c.226+3572C>T
NM_013275.6(ANKRD11):c.226+3587C>G
NM_013275.6(ANKRD11):c.2626C>T (p.Leu876Phe)
NM_013275.6(ANKRD11):c.2966C>G (p.Ser989Cys)
NM_013275.6(ANKRD11):c.3623A>G (p.Lys1208Arg)
NM_013275.6(ANKRD11):c.3715C>A (p.Pro1239Thr) rs1488664550
NM_013275.6(ANKRD11):c.3869A>C (p.His1290Pro)
NM_013275.6(ANKRD11):c.4446_4469dup (p.Gly1483_Asp1490dup) rs2151749659
NM_013275.6(ANKRD11):c.456C>G (p.Asn152Lys) rs2151796891
NM_013275.6(ANKRD11):c.4651G>A (p.Gly1551Arg)
NM_013275.6(ANKRD11):c.4892G>T (p.Arg1631Leu)
NM_013275.6(ANKRD11):c.4934T>G (p.Leu1645Arg) rs773754621
NM_013275.6(ANKRD11):c.4972A>G (p.Thr1658Ala)
NM_013275.6(ANKRD11):c.4976C>T (p.Pro1659Leu) rs754486992
NM_013275.6(ANKRD11):c.5120C>G (p.Thr1707Arg) rs776489753
NM_013275.6(ANKRD11):c.5147A>T (p.Glu1716Val)
NM_013275.6(ANKRD11):c.5206G>T (p.Val1736Leu)
NM_013275.6(ANKRD11):c.5422A>G (p.Lys1808Glu)
NM_013275.6(ANKRD11):c.5549A>T (p.Tyr1850Phe)
NM_013275.6(ANKRD11):c.559C>T (p.Leu187Phe)
NM_013275.6(ANKRD11):c.5606C>G (p.Pro1869Arg)
NM_013275.6(ANKRD11):c.5925G>A (p.Val1975=) rs761151327
NM_013275.6(ANKRD11):c.5990C>G (p.Ala1997Gly)
NM_013275.6(ANKRD11):c.6329C>T (p.Ser2110Phe)
NM_013275.6(ANKRD11):c.6772G>A (p.Ala2258Thr)
NM_013275.6(ANKRD11):c.7589G>C (p.Cys2530Ser) rs1597411259
NM_013275.6(ANKRD11):c.7607G>A (p.Arg2536Gln) rs2033511172
NM_013275.6(ANKRD11):c.7735C>T (p.Arg2579Cys) rs1567537413
NM_013275.6(ANKRD11):c.7753C>T (p.Arg2585Cys) rs1567537304
NM_013275.6(ANKRD11):c.7855G>T (p.Val2619Leu) rs2032837592
NM_013275.6(ANKRD11):c.788G>A (p.Ser263Asn)
NM_013275.6(ANKRD11):c.986A>G (p.His329Arg) rs2151766571

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