ClinVar Miner

List of variants in gene ANK3 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
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.10383A>G (p.Gln3461=) rs61732400 0.03164
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.2382+6C>A rs114581617 0.01475
NM_020987.5(ANK3):c.7140C>T (p.His2380=) rs3802696 0.01444
NM_020987.5(ANK3):c.9682G>C (p.Val3228Leu) rs61732399 0.01121
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.4122C>T (p.Ala1374=) rs12249658 0.01072
NM_020987.5(ANK3):c.7715T>C (p.Ile2572Thr) rs61732398 0.01022
NM_020987.5(ANK3):c.6483C>T (p.Val2161=) rs3134609 0.00772
NM_020987.5(ANK3):c.6473T>C (p.Ile2158Thr) rs77740274 0.00694
NM_020987.5(ANK3):c.10258C>T (p.Leu3420=) rs146174990 0.00608
NM_020987.5(ANK3):c.11505A>G (p.Leu3835=) rs78069744 0.00600
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.6011C>T (p.Ala2004Val) rs76855192 0.00564
NM_020987.5(ANK3):c.6953A>G (p.Lys2318Arg) rs59021407 0.00532
NM_020987.5(ANK3):c.13065+20G>A rs142778119 0.00477
NM_020987.5(ANK3):c.6621C>T (p.Pro2207=) rs61732396 0.00473
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.5763A>G (p.Thr1921=) rs115260634 0.00368
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.2889C>T (p.Tyr963=) rs149682716 0.00309
NM_020987.5(ANK3):c.1668G>A (p.Ala556=) rs16914613 0.00282
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.4380C>T (p.Phe1460=) rs75052415 0.00264
NM_020987.5(ANK3):c.1266C>T (p.His422=) rs2297978 0.00240
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.114+19G>A rs186021084 0.00165
NM_020987.5(ANK3):c.1492-12C>A rs41283530 0.00138
NM_020987.5(ANK3):c.5137G>A (p.Val1713Ile) rs544357242 0.00134
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.6354C>T (p.His2118=) rs116585069 0.00088
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.627G>A (p.Ala209=) rs147054068 0.00064
NM_020987.5(ANK3):c.514-3C>T rs144841334 0.00059
NM_020987.5(ANK3):c.3541-13T>C rs138231124 0.00033
NM_020987.5(ANK3):c.4403G>A (p.Arg1468His) rs74777754 0.00024
NM_020987.5(ANK3):c.115-8T>G rs186892622 0.00016
NM_020987.5(ANK3):c.11159C>T (p.Thr3720Met) rs201547988 0.00014
NM_020987.5(ANK3):c.2622T>A (p.Asp874Glu) rs564078262 0.00001
NM_020987.5(ANK3):c.11646A>G (p.Ser3882=)
NM_020987.5(ANK3):c.12144G>A (p.Ser4048=)
NM_020987.5(ANK3):c.1290C>G (p.Thr430=) rs374761322
NM_020987.5(ANK3):c.13066-12C>T
NM_020987.5(ANK3):c.1690-15dup rs34796699
NM_020987.5(ANK3):c.1690-4del rs34796699
NM_020987.5(ANK3):c.2185-13dup
NM_020987.5(ANK3):c.2614+6del rs370950407
NM_020987.5(ANK3):c.2727G>A (p.Ala909=) rs76540767
NM_020987.5(ANK3):c.2840A>C (p.Gln947Pro) rs201011715
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.415-13dup
NM_020987.5(ANK3):c.4351-10del rs761309113
NM_020987.5(ANK3):c.4351-10dup rs761309113
NM_020987.5(ANK3):c.4351-11_4351-10dup rs761309113
NM_020987.5(ANK3):c.4351-12_4351-10dup rs761309113
NM_020987.5(ANK3):c.468C>G (p.Val156=) rs71495633
NM_020987.5(ANK3):c.468C>T (p.Val156=) rs71495633
NM_020987.5(ANK3):c.898-13C>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.