ClinVar Miner

List of variants in gene ANO5 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_213599.3(ANO5):c.267T>C (p.Asp89=) rs4312063 0.83210
NM_213599.3(ANO5):c.-136G>C rs12792259 0.83191
NM_213599.3(ANO5):c.879-18T>C rs7104758 0.06440
NM_213599.3(ANO5):c.1898+29G>T rs76084798 0.02917
NM_213599.3(ANO5):c.2521-13A>G rs76850415 0.02660
NM_213599.3(ANO5):c.1120-24A>T rs11026476 0.02147
NM_213599.3(ANO5):c.2259A>G (p.Ser753=) rs61746201 0.01772
NM_213599.3(ANO5):c.1181-21T>A rs114582774 0.01015
NM_213599.3(ANO5):c.1029C>T (p.Asp343=) rs78899595 0.00992
NM_213599.3(ANO5):c.604G>A (p.Glu202Lys) rs115750596 0.00971
NM_213599.3(ANO5):c.616A>G (p.Thr206Ala) rs78266558 0.00922
NM_213599.3(ANO5):c.2387C>T (p.Ser796Leu) rs61910685 0.00804
NM_213599.3(ANO5):c.1181-48T>A rs150412089 0.00767
NM_213599.3(ANO5):c.800C>G (p.Thr267Ser) rs138144479 0.00727
NM_213599.3(ANO5):c.1545A>G (p.Ser515=) rs35843353 0.00699
NM_213599.3(ANO5):c.2354T>G (p.Leu785Arg) rs146136277 0.00524
NM_213599.3(ANO5):c.1631-35G>A rs72982041 0.00334
NM_213599.3(ANO5):c.680G>C (p.Gly227Ala) rs140903276 0.00320
NM_213599.3(ANO5):c.259G>A (p.Val87Ile) rs34994927 0.00293
NM_213599.3(ANO5):c.155A>G (p.Asn52Ser) rs143777403 0.00238
NM_213599.3(ANO5):c.1095A>G (p.Leu365=) rs35804601 0.00183
NM_213599.3(ANO5):c.2698A>C (p.Met900Leu) rs148293985 0.00169
NM_213599.3(ANO5):c.2521-7C>T rs201438159 0.00109
NM_213599.3(ANO5):c.1013+29G>C rs371272245 0.00039
NM_213599.3(ANO5):c.797C>T (p.Pro266Leu) rs745908606 0.00019
NM_213599.3(ANO5):c.2256G>A (p.Thr752=) rs144048656 0.00013
NM_213599.3(ANO5):c.674C>T (p.Pro225Leu) rs757947963 0.00006
NM_213599.3(ANO5):c.653A>G (p.Tyr218Cys) rs548449293 0.00004
NM_213599.3(ANO5):c.1227A>G (p.Glu409=) rs781554633 0.00003
NM_213599.3(ANO5):c.276A>G (p.Lys92=) rs201678262 0.00003
NM_213599.3(ANO5):c.736T>C (p.Tyr246His) rs1219063834 0.00003
NM_213599.3(ANO5):c.794A>G (p.Asn265Ser) rs377553546 0.00002
NM_213599.3(ANO5):c.1203G>T (p.Trp401Cys) rs886042339 0.00001
NM_213599.3(ANO5):c.181-16T>C rs762760550 0.00001
NM_213599.3(ANO5):c.2139C>T (p.Thr713=) rs767479331 0.00001
NM_213599.3(ANO5):c.2175T>C (p.His725=) rs1057522538 0.00001
NM_213599.3(ANO5):c.2516T>C (p.Met839Thr) rs150442899 0.00001
GRCh37/hg19 11p14.3(chr11:22069614-22252650)
NM_213599.3(ANO5):c.1222C>T (p.Leu408=) rs997655691
NM_213599.3(ANO5):c.1494T>G (p.Asp498Glu) rs2133738349
NM_213599.3(ANO5):c.181-18C>T rs1350082012
NM_213599.3(ANO5):c.1962A>G (p.Arg654=) rs1057521970
NM_213599.3(ANO5):c.2236-10del rs72105710
NM_213599.3(ANO5):c.2236-10dup rs72105710
NM_213599.3(ANO5):c.2236-11_2236-10dup rs72105710
NM_213599.3(ANO5):c.2236-12_2236-10del rs72105710
NM_213599.3(ANO5):c.2236-13_2236-10del rs72105710
NM_213599.3(ANO5):c.2415-7T>C rs1554935084
NM_213599.3(ANO5):c.2456A>G (p.Tyr819Cys) rs1554935116
NM_213599.3(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.3(ANO5):c.2688C>G (p.Ala896=) rs377549896
NM_213599.3(ANO5):c.295-16T>A rs746448319
NM_213599.3(ANO5):c.295-8dup rs778435515
NM_213599.3(ANO5):c.298A>G (p.Arg100Gly) rs1554924008
NM_213599.3(ANO5):c.364-8del rs146983312
NM_213599.3(ANO5):c.364-8dup rs146983312
NM_213599.3(ANO5):c.878+17G>A rs749031281
NM_213599.3(ANO5):c.879-7_879-6del rs143977836
NM_213599.3(ANO5):c.950C>A (p.Ala317Glu)
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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.