ClinVar Miner

List of variants in gene ANKRD11 reported as uncertain significance for autism spectrum disorder

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_013275.6(ANKRD11):c.2518C>T (p.Arg840Trp) rs761259443
NM_013275.6(ANKRD11):c.295G>A (p.Gly99Ser) rs1567593338
NM_013275.6(ANKRD11):c.3005G>A (p.Arg1002Gln) rs757870881
NM_013275.6(ANKRD11):c.3577G>A (p.Ala1193Thr) rs111737495
NM_013275.6(ANKRD11):c.3736C>T (p.His1246Tyr) rs1170311302
NM_013275.6(ANKRD11):c.3889_3891dup (p.Asn1297dup) rs778998883
NM_013275.6(ANKRD11):c.4271C>A (p.Ser1424Tyr) rs1567569737
NM_013275.6(ANKRD11):c.4401G>T (p.Glu1467Asp) rs1567569115
NM_013275.6(ANKRD11):c.4456C>T (p.Arg1486Trp) rs189656772
NM_013275.6(ANKRD11):c.449C>T (p.Thr150Met) rs777070083
NM_013275.6(ANKRD11):c.4616A>G (p.Glu1539Gly) rs751369171
NM_013275.6(ANKRD11):c.4928C>A (p.Pro1643Gln) rs147690079
NM_013275.6(ANKRD11):c.5296G>A (p.Val1766Met) rs751326964
NM_013275.6(ANKRD11):c.5716G>A (p.Ala1906Thr) rs1428749185
NM_013275.6(ANKRD11):c.5726C>T (p.Pro1909Leu) rs780224924
NM_013275.6(ANKRD11):c.5875G>A (p.Ala1959Thr) rs372148958
NM_013275.6(ANKRD11):c.5962C>T (p.Pro1988Ser) rs534220503
NM_013275.6(ANKRD11):c.6060_6061delinsGC (p.Ser2021Pro) rs1567559902
NM_013275.6(ANKRD11):c.6063_6071del (p.Pro2022_Pro2024del) rs771037147
NM_013275.6(ANKRD11):c.6232G>C (p.Asp2078His) rs1038750030
NM_013275.6(ANKRD11):c.6254G>T (p.Cys2085Phe) rs755786402
NM_013275.6(ANKRD11):c.6415C>T (p.Pro2139Ser) rs1567557350
NM_013275.6(ANKRD11):c.6448G>A (p.Asp2150Asn) rs1567557144
NM_013275.6(ANKRD11):c.6985G>C (p.Val2329Leu) rs760933701
NM_013275.6(ANKRD11):c.7087C>G (p.Pro2363Ala) rs769501453
NM_013275.6(ANKRD11):c.7167T>G (p.Phe2389Leu) rs927582667
NM_013275.6(ANKRD11):c.7198_7200dup (p.Leu2400dup) rs1371024836
NM_013275.6(ANKRD11):c.7671G>A (p.Met2557Ile) rs1567544079
NM_013275.6(ANKRD11):c.7799G>A (p.Arg2600His) rs1354874973
NM_013275.6(ANKRD11):c.7847T>C (p.Leu2616Pro) rs1567533174

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