ClinVar Miner

List of variants in gene ANK3 reported as likely benign for not specified

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_020987.5(ANK3):c.8895T>C (p.Ala2965=) rs10740006 0.18901
NM_020987.5(ANK3):c.9368A>G (p.Lys3123Arg) rs10821668 0.18742
NM_020987.5(ANK3):c.1218T>C (p.Ile406=) rs2297979 0.17447
NM_020987.5(ANK3):c.4201-3T>C rs2393595 0.12356
NM_020987.5(ANK3):c.6066C>T (p.Ala2022=) rs17208576 0.07406
NM_020987.5(ANK3):c.8655C>A (p.His2885Gln) rs11599164 0.07405
NM_020987.5(ANK3):c.9349A>G (p.Ile3117Val) rs28932171 0.07385
NM_020987.5(ANK3):c.9137C>G (p.Thr3046Ser) rs74153183 0.06794
NM_020987.5(ANK3):c.8013C>T (p.Ser2671=) rs41274674 0.04537
NM_020987.5(ANK3):c.2565T>C (p.Asn855=) rs10994234 0.03800
NM_020987.5(ANK3):c.909A>C (p.Thr303=) rs73269474 0.03053
NM_020987.5(ANK3):c.12769A>G (p.Ile4257Val) rs12261793 0.03012
NM_020987.5(ANK3):c.2124T>C (p.Asp708=) rs34552044 0.02906
NM_020987.5(ANK3):c.402T>C (p.Asn134=) rs1031688 0.02324
NM_020987.5(ANK3):c.11685C>T (p.Ser3895=) rs7923682 0.02183
NM_020987.5(ANK3):c.1491+6C>T rs76733192 0.02170
NM_020987.5(ANK3):c.8988G>C (p.Gln2996His) rs41274672 0.01542
NM_020987.5(ANK3):c.7140C>T (p.His2380=) rs3802696 0.01444
NM_020987.5(ANK3):c.382A>G (p.Thr128Ala) rs114937210 0.01080
NM_020987.5(ANK3):c.7715T>C (p.Ile2572Thr) rs61732398 0.01022
NM_020987.5(ANK3):c.2544T>C (p.Asp848=) rs60764245 0.00564
NM_020987.5(ANK3):c.7225T>C (p.Ser2409Pro) rs148904927 0.00459
NM_020987.5(ANK3):c.8508T>C (p.His2836=) rs11815168 0.00416
NM_020987.5(ANK3):c.3984G>A (p.Leu1328=) rs149052618 0.00393
NM_020987.5(ANK3):c.6955G>A (p.Asp2319Asn) rs140463162 0.00330
NM_020987.5(ANK3):c.10055A>G (p.Glu3352Gly) rs61845768 0.00329
NM_020987.5(ANK3):c.2103C>T (p.Leu701=) rs142415903 0.00280
NM_020987.5(ANK3):c.756G>A (p.Thr252=) rs117266082 0.00280
NM_020987.5(ANK3):c.2316G>A (p.Gln772=) rs143430852 0.00240
NM_020987.5(ANK3):c.2523T>C (p.Asn841=) rs144773457 0.00222
NM_020987.5(ANK3):c.2200C>T (p.Leu734=) rs144696256 0.00120
NM_020987.5(ANK3):c.3897G>A (p.Thr1299=) rs150367434 0.00106
NM_020987.5(ANK3):c.10761G>A (p.Thr3587=) rs138986388 0.00087
NM_020987.5(ANK3):c.7305T>C (p.Tyr2435=) rs115257011 0.00079
NM_020987.5(ANK3):c.399C>T (p.Val133=) rs77316697 0.00076
NM_020987.5(ANK3):c.864C>T (p.Leu288=) rs145971956 0.00029
NM_020987.5(ANK3):c.2001C>T (p.Ser667=) rs146438080 0.00022
NM_020987.5(ANK3):c.8919T>C (p.Ser2973=) rs553695085 0.00010
NM_020987.5(ANK3):c.10020C>T (p.Asp3340=) rs750349884 0.00007
NM_020987.5(ANK3):c.2721C>T (p.Leu907=) rs142825560 0.00006
NM_020987.5(ANK3):c.1644C>T (p.Ala548=) rs537093045 0.00005
NM_020987.5(ANK3):c.7986C>T (p.Ala2662=) rs147625375 0.00003
NM_020987.5(ANK3):c.429A>G (p.Pro143=) rs776144867 0.00002
NM_020987.5(ANK3):c.8883C>T (p.Pro2961=) rs765123203 0.00002
NM_020987.5(ANK3):c.297T>C (p.Asn99=) rs149618682 0.00001
NM_020987.5(ANK3):c.10302C>G (p.Leu3434=) rs1554863211
NM_020987.5(ANK3):c.11442C>G (p.Pro3814=) rs140398841
NM_020987.5(ANK3):c.1290C>G (p.Thr430=) rs374761322
NM_020987.5(ANK3):c.2614+6del rs370950407
NM_020987.5(ANK3):c.3045G>T (p.Thr1015=) rs3750800
NM_020987.5(ANK3):c.3105C>G (p.Pro1035=) rs55680239
NM_020987.5(ANK3):c.3174-5dup rs556151383
NM_020987.5(ANK3):c.4575A>G (p.Ser1525=)
NM_020987.5(ANK3):c.468C>G (p.Val156=) rs71495633
NM_020987.5(ANK3):c.9456T>C (p.Thr3152=) rs41274670

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