ClinVar Miner

Variants in gene ANK3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 51
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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.10953A>C (p.Lys3651Asn) rs115903343 0.01085
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.2615-6882A>G rs41283526 0.00832
NM_020987.5(ANK3):c.1047C>T (p.Cys349=) rs117138204 0.00580
NM_020987.5(ANK3):c.2544T>C (p.Asp848=) rs60764245 0.00564
NM_020987.5(ANK3):c.6953A>G (p.Lys2318Arg) rs59021407 0.00532
NM_020987.5(ANK3):c.13106G>A (p.Arg4369Gln) rs141939315 0.00503
NM_020987.5(ANK3):c.13065+20G>A rs142778119 0.00477
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.2322G>C (p.Gly774=) rs138823660 0.00344
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.2889C>T (p.Tyr963=) rs149682716 0.00309
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.2674T>C (p.Leu892=) rs61732401 0.00273
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.1492-12C>A rs41283530 0.00138
NM_020987.5(ANK3):c.8534G>A (p.Gly2845Glu) rs139022925 0.00126
NM_020987.5(ANK3):c.2200C>T (p.Leu734=) rs144696256 0.00120
NM_020987.5(ANK3):c.4029G>A (p.Glu1343=) rs116757606 0.00114
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.12596-355G>T
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.468C>G (p.Val156=) rs71495633

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