Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6291877G>ACA549423230WFS1c.632-40G>A (n.632-40G>A)
c.609-40G>A
c.383-40G>A (n.383-40G>A)
c.431-40G>A (n.431-40G>A)
c.229-40G>A
n.817-40G>A
c.641-40G>A (n.641-40G>A)
 dbSNP gnomAD v2
4g.6291877G=CA1435768926WFS1c.632-40G= (n.632-40G=)
c.609-40G=
c.383-40G= (n.383-40G=)
c.431-40G= (n.431-40G=)
c.229-40G=
n.817-40G=
c.641-40G= (n.641-40G=)
4g.6291877G>TCA648576148WFS1c.632-40G>T (n.632-40G>T)
c.609-40G>T
c.383-40G>T (n.383-40G>T)
c.431-40G>T (n.431-40G>T)
c.229-40G>T
n.817-40G>T
c.641-40G>T (n.641-40G>T)
 COSMIC
4g.6291878T>ACA2669826213WFS1c.632-39T>A (n.632-39T>A)
c.609-39T>A
c.383-39T>A (n.383-39T>A)
c.431-39T>A (n.431-39T>A)
c.229-39T>A
n.817-39T>A
c.641-39T>A (n.641-39T>A)
 gnomAD v4
4g.6291879C>ACA2838980WFS1c.632-38C>A (n.632-38C>A)
c.609-38C>A
c.383-38C>A (n.383-38C>A)
c.431-38C>A (n.431-38C>A)
c.229-38C>A
n.817-38C>A
c.641-38C>A (n.641-38C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291879C=CA1435768927WFS1c.632-38C= (n.632-38C=)
c.609-38C=
c.383-38C= (n.383-38C=)
c.431-38C= (n.431-38C=)
c.229-38C=
n.817-38C=
c.641-38C= (n.641-38C=)
4g.6291879C>GCA549423233WFS1c.632-38C>G (n.632-38C>G)
c.609-38C>G
c.383-38C>G (n.383-38C>G)
c.431-38C>G (n.431-38C>G)
c.229-38C>G
n.817-38C>G
c.641-38C>G (n.641-38C>G)
 dbSNP gnomAD v2 gnomAD v4
4g.6291880A>GCA2669826214WFS1c.632-37A>G (n.632-37A>G)
c.609-37A>G
c.383-37A>G (n.383-37A>G)
c.431-37A>G (n.431-37A>G)
c.229-37A>G
n.817-37A>G
c.641-37A>G (n.641-37A>G)
 gnomAD v4
4g.6291882C>ACA2669826215WFS1c.632-35C>A (n.632-35C>A)
c.609-35C>A
c.383-35C>A (n.383-35C>A)
c.431-35C>A (n.431-35C>A)
c.229-35C>A
n.817-35C>A
c.641-35C>A (n.641-35C>A)
 gnomAD v4
4g.6291882C=CA1435768928WFS1c.632-35C= (n.632-35C=)
c.609-35C=
c.383-35C= (n.383-35C=)
c.431-35C= (n.431-35C=)
c.229-35C=
n.817-35C=
c.641-35C= (n.641-35C=)
4g.6291882C>GCA2669826216WFS1c.632-35C>G (n.632-35C>G)
c.609-35C>G
c.383-35C>G (n.383-35C>G)
c.431-35C>G (n.431-35C>G)
c.229-35C>G
n.817-35C>G
c.641-35C>G (n.641-35C>G)
 gnomAD v4
4g.6291882C>TCA549423234WFS1c.632-35C>T (n.632-35C>T)
c.609-35C>T
c.383-35C>T (n.383-35C>T)
c.431-35C>T (n.431-35C>T)
c.229-35C>T
n.817-35C>T
c.641-35C>T (n.641-35C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6291883T>CCA2705215301WFS1c.632-34T>C (n.632-34T>C)
c.609-34T>C
c.383-34T>C (n.383-34T>C)
c.431-34T>C (n.431-34T>C)
c.229-34T>C
n.817-34T>C
c.641-34T>C (n.641-34T>C)
 dbSNP
4g.6291886T>GCA2669826217WFS1c.632-31T>G (n.632-31T>G)
c.609-31T>G
c.383-31T>G (n.383-31T>G)
c.431-31T>G (n.431-31T>G)
c.229-31T>G
n.817-31T>G
c.641-31T>G (n.641-31T>G)
 gnomAD v4
4g.6291886_6291890delinsTCTGACA1435768929WFS1c.632-31_632-27delinsTCTGA (n.632-31_632-27delinsTCTGA)
c.609-31_609-27delinsTCTGA
c.383-31_383-27delinsTCTGA (n.383-31_383-27delinsTCTGA)
c.431-31_431-27delinsTCTGA (n.431-31_431-27delinsTCTGA)
c.229-31_229-27delinsTCTGA
n.817-31_817-27delinsTCTGA
c.641-31_641-27delinsTCTGA (n.641-31_641-27delinsTCTGA)
4g.6291887C>ACA2578035776WFS1c.632-30C>A (n.632-30C>A)
c.609-30C>A
c.383-30C>A (n.383-30C>A)
c.431-30C>A (n.431-30C>A)
c.229-30C>A
n.817-30C>A
c.641-30C>A (n.641-30C>A)
 gnomAD v4
4g.6291887C>GCA2669826218WFS1c.632-30C>G (n.632-30C>G)
c.609-30C>G
c.383-30C>G (n.383-30C>G)
c.431-30C>G (n.431-30C>G)
c.229-30C>G
n.817-30C>G
c.641-30C>G (n.641-30C>G)
 gnomAD v4
4g.6291890_6291893delCA2838981WFS1c.632-27_632-24del (n.632-27_632-24del)
c.609-27_609-24del
c.383-27_383-24del (n.383-27_383-24del)
c.431-27_431-24del (n.431-27_431-24del)
c.229-27_229-24del
n.817-27_817-24del
c.641-27_641-24del (n.641-27_641-24del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291887_6291888insGACA2669826219WFS1c.632-30_632-29insGA (n.632-30_632-29insGA)
c.609-30_609-29insGA
c.383-30_383-29insGA (n.383-30_383-29insGA)
c.431-30_431-29insGA (n.431-30_431-29insGA)
c.229-30_229-29insGA
n.817-30_817-29insGA
c.641-30_641-29insGA (n.641-30_641-29insGA)
 gnomAD v4
4g.6291888T>CCA2669826220WFS1c.632-29T>C (n.632-29T>C)
c.609-29T>C
c.383-29T>C (n.383-29T>C)
c.431-29T>C (n.431-29T>C)
c.229-29T>C
n.817-29T>C
c.641-29T>C (n.641-29T>C)
 gnomAD v4
4g.6291889G>TCA2669826221WFS1c.632-28G>T (n.632-28G>T)
c.609-28G>T
c.383-28G>T (n.383-28G>T)
c.431-28G>T (n.431-28G>T)
c.229-28G>T
n.817-28G>T
c.641-28G>T (n.641-28G>T)
 gnomAD v4
4g.6291891C>ACA2669826222WFS1c.632-26C>A (n.632-26C>A)
c.609-26C>A
c.383-26C>A (n.383-26C>A)
c.431-26C>A (n.431-26C>A)
c.229-26C>A
n.817-26C>A
c.641-26C>A (n.641-26C>A)
 gnomAD v4
4g.6291891C>GCA2578035777WFS1c.632-26C>G (n.632-26C>G)
c.609-26C>G
c.383-26C>G (n.383-26C>G)
c.431-26C>G (n.431-26C>G)
c.229-26C>G
n.817-26C>G
c.641-26C>G (n.641-26C>G)
 gnomAD v4
4g.6291891_6291893delinsCTGCA1435768930WFS1c.632-26_632-24delinsCTG (n.632-26_632-24delinsCTG)
c.609-26_609-24delinsCTG
c.383-26_383-24delinsCTG (n.383-26_383-24delinsCTG)
c.431-26_431-24delinsCTG (n.431-26_431-24delinsCTG)
c.229-26_229-24delinsCTG
n.817-26_817-24delinsCTG
c.641-26_641-24delinsCTG (n.641-26_641-24delinsCTG)
4g.6291892T>CCA1435768932WFS1c.632-25T>C (n.632-25T>C)
c.609-25T>C
c.383-25T>C (n.383-25T>C)
c.431-25T>C (n.431-25T>C)
c.229-25T>C
n.817-25T>C
c.641-25T>C (n.641-25T>C)
 dbSNP
4g.6291892T=CA1435768931WFS1c.632-25T= (n.632-25T=)
c.609-25T=
c.383-25T= (n.383-25T=)
c.431-25T= (n.431-25T=)
c.229-25T=
n.817-25T=
c.641-25T= (n.641-25T=)
4g.6291893_6291894delCA91794665WFS1c.632-24_632-23del (n.632-24_632-23del)
c.609-24_609-23del
c.383-24_383-23del (n.383-24_383-23del)
c.431-24_431-23del (n.431-24_431-23del)
c.229-24_229-23del
n.817-24_817-23del
c.641-24_641-23del (n.641-24_641-23del)
 dbSNP
4g.6291893G>ACA549423238WFS1c.632-24G>A (n.632-24G>A)
c.609-24G>A
c.383-24G>A (n.383-24G>A)
c.431-24G>A (n.431-24G>A)
c.229-24G>A
n.817-24G>A
c.641-24G>A (n.641-24G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6291893G>CCA2669826223WFS1c.632-24G>C (n.632-24G>C)
c.609-24G>C
c.383-24G>C (n.383-24G>C)
c.431-24G>C (n.431-24G>C)
c.229-24G>C
n.817-24G>C
c.641-24G>C (n.641-24G>C)
 gnomAD v4
4g.6291893G=CA1435768933WFS1c.632-24G= (n.632-24G=)
c.609-24G=
c.383-24G= (n.383-24G=)
c.431-24G= (n.431-24G=)
c.229-24G=
n.817-24G=
c.641-24G= (n.641-24G=)
4g.6291893G>TCA2669826224WFS1c.632-24G>T (n.632-24G>T)
c.609-24G>T
c.383-24G>T (n.383-24G>T)
c.431-24G>T (n.431-24G>T)
c.229-24G>T
n.817-24G>T
c.641-24G>T (n.641-24G>T)
 gnomAD v4
4g.6291896A>TCA2669826225WFS1c.632-21A>T (n.632-21A>T)
c.609-21A>T
c.383-21A>T (n.383-21A>T)
c.431-21A>T (n.431-21A>T)
c.229-21A>T
n.817-21A>T
c.641-21A>T (n.641-21A>T)
 gnomAD v4
4g.6291897A=CA1435768934WFS1c.632-20A= (n.632-20A=)
c.609-20A=
c.383-20A= (n.383-20A=)
c.431-20A= (n.431-20A=)
c.229-20A=
n.817-20A=
c.641-20A= (n.641-20A=)
4g.6291897A>GCA549423239WFS1c.632-20A>G (n.632-20A>G)
c.609-20A>G
c.383-20A>G (n.383-20A>G)
c.431-20A>G (n.431-20A>G)
c.229-20A>G
n.817-20A>G
c.641-20A>G (n.641-20A>G)
 dbSNP gnomAD v2
4g.6291898T>ACA2669826226WFS1c.632-19T>A (n.632-19T>A)
c.609-19T>A
c.383-19T>A (n.383-19T>A)
c.431-19T>A (n.431-19T>A)
c.229-19T>A
n.817-19T>A
c.641-19T>A (n.641-19T>A)
 gnomAD v4
4g.6291899C>ACA2669826228WFS1c.632-18C>A (n.632-18C>A)
c.609-18C>A
c.383-18C>A (n.383-18C>A)
c.431-18C>A (n.431-18C>A)
c.229-18C>A
n.817-18C>A
c.641-18C>A (n.641-18C>A)
 gnomAD v4
4g.6291899C>GCA2669826227WFS1c.632-18C>G (n.632-18C>G)
c.609-18C>G
c.383-18C>G (n.383-18C>G)
c.431-18C>G (n.431-18C>G)
c.229-18C>G
n.817-18C>G
c.641-18C>G (n.641-18C>G)
 gnomAD v4
4g.6291900C=CA1435768935WFS1c.632-17C= (n.632-17C=)
c.609-17C=
c.383-17C= (n.383-17C=)
c.431-17C= (n.431-17C=)
c.229-17C=
n.817-17C=
c.641-17C= (n.641-17C=)
4g.6291900C>TCA1058889000WFS1c.632-17C>T (n.632-17C>T)
c.609-17C>T
c.383-17C>T (n.383-17C>T)
c.431-17C>T (n.431-17C>T)
c.229-17C>T
n.817-17C>T
c.641-17C>T (n.641-17C>T)
 dbSNP gnomAD v3 gnomAD v4
4g.6291901A=CA1435768936WFS1c.632-16A= (n.632-16A=)
c.609-16A=
c.383-16A= (n.383-16A=)
c.431-16A= (n.431-16A=)
c.229-16A=
n.817-16A=
c.641-16A= (n.641-16A=)
4g.6291901A>CCA1435768937WFS1c.632-16A>C (n.632-16A>C)
c.609-16A>C
c.383-16A>C (n.383-16A>C)
c.431-16A>C (n.431-16A>C)
c.229-16A>C
n.817-16A>C
c.641-16A>C (n.641-16A>C)
 dbSNP
4g.6291902C>ACA2669826229WFS1c.632-15C>A (n.632-15C>A)
c.609-15C>A
c.383-15C>A (n.383-15C>A)
c.431-15C>A (n.431-15C>A)
c.229-15C>A
n.817-15C>A
c.641-15C>A (n.641-15C>A)
 gnomAD v4
4g.6291902C>TCA2760284189WFS1c.632-15C>T (n.632-15C>T)
c.609-15C>T
c.383-15C>T (n.383-15C>T)
c.431-15C>T (n.431-15C>T)
c.229-15C>T
n.817-15C>T
c.641-15C>T (n.641-15C>T)
4g.6291903C>ACA2669826230WFS1c.632-14C>A (n.632-14C>A)
c.609-14C>A
c.383-14C>A (n.383-14C>A)
c.431-14C>A (n.431-14C>A)
c.229-14C>A
n.817-14C>A
c.641-14C>A (n.641-14C>A)
 gnomAD v4
4g.6291903C=CA1435768939WFS1c.632-14C= (n.632-14C=)
c.609-14C=
c.383-14C= (n.383-14C=)
c.431-14C= (n.431-14C=)
c.229-14C=
n.817-14C=
c.641-14C= (n.641-14C=)
4g.6291903C>TCA91794666WFS1c.632-14C>T (n.632-14C>T)
c.609-14C>T
c.383-14C>T (n.383-14C>T)
c.431-14C>T (n.431-14C>T)
c.229-14C>T
n.817-14C>T
c.641-14C>T (n.641-14C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6291903_6291905delinsCCTCA1435768938WFS1c.632-14_632-12delinsCCT (n.632-14_632-12delinsCCT)
c.609-14_609-12delinsCCT
c.383-14_383-12delinsCCT (n.383-14_383-12delinsCCT)
c.431-14_431-12delinsCCT (n.431-14_431-12delinsCCT)
c.229-14_229-12delinsCCT
n.817-14_817-12delinsCCT
c.641-14_641-12delinsCCT (n.641-14_641-12delinsCCT)
4g.6291904C>ACA2669826231WFS1c.632-13C>A (n.632-13C>A)
c.609-13C>A
c.383-13C>A (n.383-13C>A)
c.431-13C>A (n.431-13C>A)
c.229-13C>A
n.817-13C>A
c.641-13C>A (n.641-13C>A)
 gnomAD v4
4g.6291904_6291905delCA91794667WFS1c.632-13_632-12del (n.632-13_632-12del)
c.609-13_609-12del
c.383-13_383-12del (n.383-13_383-12del)
c.431-13_431-12del (n.431-13_431-12del)
c.229-13_229-12del
n.817-13_817-12del
c.641-13_641-12del (n.641-13_641-12del)
 dbSNP
4g.6291907T>ACA2760284190WFS1c.632-10T>A (n.632-10T>A)
c.609-10T>A
c.383-10T>A (n.383-10T>A)
c.431-10T>A (n.431-10T>A)
c.229-10T>A
n.817-10T>A
c.641-10T>A (n.641-10T>A)
4g.6291907T>GCA2580071768WFS1c.632-10T>G (n.632-10T>G)
c.609-10T>G
c.383-10T>G (n.383-10T>G)
c.431-10T>G (n.431-10T>G)
c.229-10T>G
n.817-10T>G
c.641-10T>G (n.641-10T>G)
 ClinVar
4g.6291908C>ACA2669826232WFS1c.632-9C>A (n.632-9C>A)
c.609-9C>A
c.383-9C>A (n.383-9C>A)
c.431-9C>A (n.431-9C>A)
c.229-9C>A
n.817-9C>A
c.641-9C>A (n.641-9C>A)
 gnomAD v4
4g.6291908C=CA1435768940WFS1c.632-9C= (n.632-9C=)
c.609-9C=
c.383-9C= (n.383-9C=)
c.431-9C= (n.431-9C=)
c.229-9C=
n.817-9C=
c.641-9C= (n.641-9C=)
4g.6291908C>TCA91794668WFS1c.632-9C>T (n.632-9C>T)
c.609-9C>T
c.383-9C>T (n.383-9C>T)
c.431-9C>T (n.431-9C>T)
c.229-9C>T
n.817-9C>T
c.641-9C>T (n.641-9C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6291909C>ACA2580071769WFS1c.632-8C>A (n.632-8C>A)
c.609-8C>A
c.383-8C>A (n.383-8C>A)
c.431-8C>A (n.431-8C>A)
c.229-8C>A
n.817-8C>A
c.641-8C>A (n.641-8C>A)
 ClinVar
4g.6291909C>GCA2578035778WFS1c.632-8C>G (n.632-8C>G)
c.609-8C>G
c.383-8C>G (n.383-8C>G)
c.431-8C>G (n.431-8C>G)
c.229-8C>G
n.817-8C>G
c.641-8C>G (n.641-8C>G)
4g.6291909C>TCA2573138319WFS1c.632-8C>T (n.632-8C>T)
c.609-8C>T
c.383-8C>T (n.383-8C>T)
c.431-8C>T (n.431-8C>T)
c.229-8C>T
n.817-8C>T
c.641-8C>T (n.641-8C>T)
 ClinVar dbSNP gnomAD v4
4g.6291910C=CA1435768941WFS1c.632-7C= (n.632-7C=)
c.609-7C=
c.383-7C= (n.383-7C=)
c.431-7C= (n.431-7C=)
c.229-7C=
n.817-7C=
c.641-7C= (n.641-7C=)
4g.6291910C>GCA549423242WFS1c.632-7C>G (n.632-7C>G)
c.609-7C>G
c.383-7C>G (n.383-7C>G)
c.431-7C>G (n.431-7C>G)
c.229-7C>G
n.817-7C>G
c.641-7C>G (n.641-7C>G)
 dbSNP gnomAD v2 gnomAD v4
4g.6291910C>TCA2669826233WFS1c.632-7C>T (n.632-7C>T)
c.609-7C>T
c.383-7C>T (n.383-7C>T)
c.431-7C>T (n.431-7C>T)
c.229-7C>T
n.817-7C>T
c.641-7C>T (n.641-7C>T)
 gnomAD v4
4g.6291911C>ACA2669826234WFS1c.632-6C>A (n.632-6C>A)
c.609-6C>A
c.383-6C>A (n.383-6C>A)
c.431-6C>A (n.431-6C>A)
c.229-6C>A
n.817-6C>A
c.641-6C>A (n.641-6C>A)
 gnomAD v4
4g.6291912T>CCA915944124WFS1c.632-5T>C (n.632-5T>C)
c.609-5T>C
c.383-5T>C (n.383-5T>C)
c.431-5T>C (n.431-5T>C)
c.229-5T>C
n.817-5T>C
c.641-5T>C (n.641-5T>C)
 ClinVar dbSNP gnomAD v4
4g.6291912T=CA1435768942WFS1c.632-5T= (n.632-5T=)
c.609-5T=
c.383-5T= (n.383-5T=)
c.431-5T= (n.431-5T=)
c.229-5T=
n.817-5T=
c.641-5T= (n.641-5T=)
4g.6291913G>ACA2669826235WFS1c.632-4G>A (n.632-4G>A)
c.609-4G>A
c.383-4G>A (n.383-4G>A)
c.431-4G>A (n.431-4G>A)
c.229-4G>A
n.817-4G>A
c.641-4G>A (n.641-4G>A)
 gnomAD v4
4g.6291914C>ACA2669826236WFS1c.632-3C>A (n.632-3C>A)
c.609-3C>A
c.383-3C>A (n.383-3C>A)
c.431-3C>A (n.431-3C>A)
c.229-3C>A
n.817-3C>A
c.641-3C>A (n.641-3C>A)
 gnomAD v4
4g.6291914C>TCA2669826237WFS1c.632-3C>T (n.632-3C>T)
c.609-3C>T
c.383-3C>T (n.383-3C>T)
c.431-3C>T (n.431-3C>T)
c.229-3C>T
n.817-3C>T
c.641-3C>T (n.641-3C>T)
 gnomAD v4
4g.6291915A>CCA356172192WFS1c.632-2A>C (n.632-2A>C)
c.609-2A>C
c.383-2A>C (n.383-2A>C)
c.431-2A>C (n.431-2A>C)
c.229-2A>C
n.817-2A>C
c.641-2A>C (n.641-2A>C)
4g.6291915A>GCA356172193WFS1c.632-2A>G (n.632-2A>G)
c.609-2A>G
c.383-2A>G (n.383-2A>G)
c.431-2A>G (n.431-2A>G)
c.229-2A>G
n.817-2A>G
c.641-2A>G (n.641-2A>G)
4g.6291915A>TCA356172194WFS1c.632-2A>T (n.632-2A>T)
c.609-2A>T
c.383-2A>T (n.383-2A>T)
c.431-2A>T (n.431-2A>T)
c.229-2A>T
n.817-2A>T
c.641-2A>T (n.641-2A>T)
4g.6291916G>ACA356172195WFS1c.632-1G>A (n.632-1G>A)
c.609-1G>A
c.383-1G>A (n.383-1G>A)
c.431-1G>A (n.431-1G>A)
c.229-1G>A
n.817-1G>A
c.641-1G>A (n.641-1G>A)
4g.6291916G>CCA356172196WFS1c.632-1G>C (n.632-1G>C)
c.609-1G>C
c.383-1G>C (n.383-1G>C)
c.431-1G>C (n.431-1G>C)
c.229-1G>C
n.817-1G>C
c.641-1G>C (n.641-1G>C)
4g.6291916G>TCA356172197WFS1c.632-1G>T (n.632-1G>T)
c.609-1G>T
c.383-1G>T (n.383-1G>T)
c.431-1G>T (n.431-1G>T)
c.229-1G>T
n.817-1G>T
c.641-1G>T (n.641-1G>T)
 gnomAD v4
4g.6291917A>CCA356172198WFS1c.632A>C (p.Asp211Ala)
c.609A>C
c.383A>C (p.Asp128Ala)
c.431A>C (p.Asp144Ala)
c.229A>C
n.817A>C
c.641A>C (p.Asp214Ala)
4g.6291917A>GCA356172199WFS1c.632A>G (p.Asp211Gly)
c.609A>G
c.383A>G (p.Asp128Gly)
c.431A>G (p.Asp144Gly)
c.229A>G
n.817A>G
c.641A>G (p.Asp214Gly)
 ClinVar dbSNP gnomAD v4
4g.6291917A>TCA356172200WFS1c.632A>T (p.Asp211Val)
c.609A>T
c.383A>T (p.Asp128Val)
c.431A>T (p.Asp144Val)
c.229A>T
n.817A>T
c.641A>T (p.Asp214Val)
4g.6291918T>ACA356172201WFS1c.633T>A (p.Asp211Glu)
c.610T>A
c.384T>A (p.Asp128Glu)
c.432T>A (p.Asp144Glu)
c.230T>A
n.818T>A
c.642T>A (p.Asp214Glu)
4g.6291918T>CCA438211036WFS1c.633T>C (p.Asp211=)
c.610T>C
c.384T>C (p.Asp128=)
c.432T>C (p.Asp144=)
c.230T>C
n.818T>C
c.642T>C (p.Asp214=)
4g.6291918T>GCA356172202WFS1c.633T>G (p.Asp211Glu)
c.610T>G
c.384T>G (p.Asp128Glu)
c.432T>G (p.Asp144Glu)
c.230T>G
n.818T>G
c.642T>G (p.Asp214Glu)
4g.6291918_6291919delinsTGCA1435768943WFS1c.633_634delinsTG (p.Asp211=)
c.610_611delinsTG
c.384_385delinsTG (p.Asp128=)
c.432_433delinsTG (p.Asp144=)
c.230_231delinsTG
n.818_819delinsTG
c.642_643delinsTG (p.Asp214=)
4g.6291919G>ACA356172205WFS1c.634G>A (p.Gly212Arg)
c.611G>A
c.385G>A (p.Gly129Arg)
c.433G>A (p.Gly145Arg)
c.231G>A
n.819G>A
c.643G>A (p.Gly215Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6291919G>CCA356172204WFS1c.634G>C (p.Gly212Arg)
c.611G>C
c.385G>C (p.Gly129Arg)
c.433G>C (p.Gly145Arg)
c.231G>C
n.819G>C
c.643G>C (p.Gly215Arg)
4g.6291919G=CA1435768945WFS1c.634G= (p.Gly212=)
c.611G=
c.385G= (p.Gly129=)
c.433G= (p.Gly145=)
c.231G=
n.819G=
c.643G= (p.Gly215=)
4g.6291919G>TCA356172203WFS1c.634G>T (p.Gly212Ter)
c.611G>T
c.385G>T (p.Gly129Ter)
c.433G>T (p.Gly145Ter)
c.231G>T
n.819G>T
c.643G>T (p.Gly215Ter)
4g.6291920delCA1435768944WFS1c.635del (p.Gly212GlufsTer?)
c.612del
c.386del (p.Gly129GlufsTer?)
c.434del (p.Gly145GlufsTer?)
c.232del
n.820del
c.644del (p.Gly215GlufsTer?)
 dbSNP
4g.6291920G>ACA356172206WFS1c.635G>A (p.Gly212Glu)
c.612G>A
c.386G>A (p.Gly129Glu)
c.434G>A (p.Gly145Glu)
c.232G>A
n.820G>A
c.644G>A (p.Gly215Glu)
 gnomAD v4
4g.6291920G>CCA356172207WFS1c.635G>C (p.Gly212Ala)
c.612G>C
c.386G>C (p.Gly129Ala)
c.434G>C (p.Gly145Ala)
c.232G>C
n.820G>C
c.644G>C (p.Gly215Ala)
4g.6291920G>TCA356172208WFS1c.635G>T (p.Gly212Val)
c.612G>T
c.386G>T (p.Gly129Val)
c.434G>T (p.Gly145Val)
c.232G>T
n.820G>T
c.644G>T (p.Gly215Val)
 gnomAD v4
4g.6291921A>CCA438211038WFS1c.636A>C (p.Gly212=)
c.613A>C
c.387A>C (p.Gly129=)
c.435A>C (p.Gly145=)
c.233A>C
n.821A>C
c.645A>C (p.Gly215=)
4g.6291921A>GCA438211039WFS1c.636A>G (p.Gly212=)
c.613A>G
c.387A>G (p.Gly129=)
c.435A>G (p.Gly145=)
c.233A>G
n.821A>G
c.645A>G (p.Gly215=)
 gnomAD v4
4g.6291921A>TCA438211040WFS1c.636A>T (p.Gly212=)
c.613A>T
c.387A>T (p.Gly129=)
c.435A>T (p.Gly145=)
c.233A>T
n.821A>T
c.645A>T (p.Gly215=)
4g.6291922G>ACA356172209WFS1c.637G>A (p.Gly213Arg)
c.614G>A
c.388G>A (p.Gly130Arg)
c.436G>A (p.Gly146Arg)
c.234G>A
n.822G>A
c.646G>A (p.Gly216Arg)
 gnomAD v4
4g.6291922G>CCA356172210WFS1c.637G>C (p.Gly213Arg)
c.614G>C
c.388G>C (p.Gly130Arg)
c.436G>C (p.Gly146Arg)
c.234G>C
n.822G>C
c.646G>C (p.Gly216Arg)
4g.6291922G>TCA356172211WFS1c.637G>T (p.Gly213Trp)
c.614G>T
c.388G>T (p.Gly130Trp)
c.436G>T (p.Gly146Trp)
c.234G>T
n.822G>T
c.646G>T (p.Gly216Trp)
 gnomAD v4
4g.6291923G>ACA2838982WFS1c.638G>A (p.Gly213Glu)
c.615G>A
c.389G>A (p.Gly130Glu)
c.437G>A (p.Gly146Glu)
c.235G>A
n.823G>A
c.647G>A (p.Gly216Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6291923G>CCA356172212WFS1c.638G>C (p.Gly213Ala)
c.615G>C
c.389G>C (p.Gly130Ala)
c.437G>C (p.Gly146Ala)
c.235G>C
n.823G>C
c.647G>C (p.Gly216Ala)
4g.6291923G=CA1435768946WFS1c.638G= (p.Gly213=)
c.615G=
c.389G= (p.Gly130=)
c.437G= (p.Gly146=)
c.235G=
n.823G=
c.647G= (p.Gly216=)
4g.6291923G>TCA356172213WFS1c.638G>T (p.Gly213Val)
c.615G>T
c.389G>T (p.Gly130Val)
c.437G>T (p.Gly146Val)
c.235G>T
n.823G>T
c.647G>T (p.Gly216Val)
4g.6291924_6291927delCA2586973597WFS1c.639_642del (p.Ala214SerfsTer?)
c.616_619del
c.390_393del (p.Ala131SerfsTer?)
c.438_441del (p.Ala147SerfsTer?)
c.236_239del
n.824_827del
c.648_651del (p.Ala217SerfsTer?)
4g.6291924G>ACA438211041WFS1c.639G>A (p.Gly213=)
c.616G>A
c.390G>A (p.Gly130=)
c.438G>A (p.Gly146=)
c.236G>A
n.824G>A
c.648G>A (p.Gly216=)
4g.6291924G>CCA438211042WFS1c.639G>C (p.Gly213=)
c.616G>C
c.390G>C (p.Gly130=)
c.438G>C (p.Gly146=)
c.236G>C
n.824G>C
c.648G>C (p.Gly216=)
4g.6291924G>TCA438211043WFS1c.639G>T (p.Gly213=)
c.616G>T
c.390G>T (p.Gly130=)
c.438G>T (p.Gly146=)
c.236G>T
n.824G>T
c.648G>T (p.Gly216=)
4g.6291925G>ACA356172214WFS1c.640G>A (p.Ala214Thr)
c.617G>A
c.391G>A (p.Ala131Thr)
c.439G>A (p.Ala147Thr)
c.237G>A
n.825G>A
c.649G>A (p.Ala217Thr)
4g.6291925G>CCA356172215WFS1c.640G>C (p.Ala214Pro)
c.617G>C
c.391G>C (p.Ala131Pro)
c.439G>C (p.Ala147Pro)
c.237G>C
n.825G>C
c.649G>C (p.Ala217Pro)
4g.6291925G>TCA356172216WFS1c.640G>T (p.Ala214Ser)
c.617G>T
c.391G>T (p.Ala131Ser)
c.439G>T (p.Ala147Ser)
c.237G>T
n.825G>T
c.649G>T (p.Ala217Ser)
4g.6291926C>ACA356172217WFS1c.641C>A (p.Ala214Glu)
c.618C>A
c.392C>A (p.Ala131Glu)
c.440C>A (p.Ala147Glu)
c.238C>A
n.826C>A
c.650C>A (p.Ala217Glu)
4g.6291926C=CA1435768947WFS1c.641C= (p.Ala214=)
c.618C=
c.392C= (p.Ala131=)
c.440C= (p.Ala147=)
c.238C=
n.826C=
c.650C= (p.Ala217=)
4g.6291926C>GCA356172218WFS1c.641C>G (p.Ala214Gly)
c.618C>G
c.392C>G (p.Ala131Gly)
c.440C>G (p.Ala147Gly)
c.238C>G
n.826C>G
c.650C>G (p.Ala217Gly)
 ClinVar dbSNP
4g.6291926C>TCA2838983WFS1c.641C>T (p.Ala214Val)
c.618C>T
c.392C>T (p.Ala131Val)
c.440C>T (p.Ala147Val)
c.238C>T
n.826C>T
c.650C>T (p.Ala217Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291927G>ACA2838984WFS1c.642G>A (p.Ala214=)
c.619G>A
c.393G>A (p.Ala131=)
c.441G>A (p.Ala147=)
c.239G>A
n.827G>A
c.651G>A (p.Ala217=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291927G>CCA438211044WFS1c.642G>C (p.Ala214=)
c.619G>C
c.393G>C (p.Ala131=)
c.441G>C (p.Ala147=)
c.239G>C
n.827G>C
c.651G>C (p.Ala217=)
4g.6291927G=CA1435768948WFS1c.642G= (p.Ala214=)
c.619G=
c.393G= (p.Ala131=)
c.441G= (p.Ala147=)
c.239G=
n.827G=
c.651G= (p.Ala217=)
4g.6291927G>TCA438211045WFS1c.642G>T (p.Ala214=)
c.619G>T
c.393G>T (p.Ala131=)
c.441G>T (p.Ala147=)
c.239G>T
n.827G>T
c.651G>T (p.Ala217=)
4g.6291928C>ACA356172220WFS1c.643C>A (p.Gln215Lys)
c.620C>A
c.394C>A (p.Gln132Lys)
c.442C>A (p.Gln148Lys)
c.240C>A
n.828C>A
c.652C>A (p.Gln218Lys)
4g.6291928C=CA1435768949WFS1c.643C= (p.Gln215=)
c.620C=
c.394C= (p.Gln132=)
c.442C= (p.Gln148=)
c.240C=
n.828C=
c.652C= (p.Gln218=)
4g.6291928C>GCA356172219WFS1c.643C>G (p.Gln215Glu)
c.620C>G
c.394C>G (p.Gln132Glu)
c.442C>G (p.Gln148Glu)
c.240C>G
n.828C>G
c.652C>G (p.Gln218Glu)
4g.6291928C>TCA2838985WFS1c.643C>T (p.Gln215Ter)
c.620C>T
c.394C>T (p.Gln132Ter)
c.442C>T (p.Gln148Ter)
c.240C>T
n.828C>T
c.652C>T (p.Gln218Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6291931_6291934delCA2578035779WFS1c.646_649del (p.Pro216AlafsTer?)
c.623_626del
c.397_400del (p.Pro133AlafsTer?)
c.445_448del (p.Pro149AlafsTer?)
c.243_246del
n.831_834del
c.655_658del (p.Pro219AlafsTer?)
 gnomAD v4
4g.6291929A>CCA356172221WFS1c.644A>C (p.Gln215Pro)
c.621A>C
c.395A>C (p.Gln132Pro)
c.443A>C (p.Gln148Pro)
c.241A>C
n.829A>C
c.653A>C (p.Gln218Pro)
4g.6291929A>GCA356172222WFS1c.644A>G (p.Gln215Arg)
c.621A>G
c.395A>G (p.Gln132Arg)
c.443A>G (p.Gln148Arg)
c.241A>G
n.829A>G
c.653A>G (p.Gln218Arg)
4g.6291929A>TCA356172223WFS1c.644A>T (p.Gln215Leu)
c.621A>T
c.395A>T (p.Gln132Leu)
c.443A>T (p.Gln148Leu)
c.241A>T
n.829A>T
c.653A>T (p.Gln218Leu)
4g.6291930G>ACA438211046WFS1c.645G>A (p.Gln215=)
c.622G>A
c.396G>A (p.Gln132=)
c.444G>A (p.Gln148=)
c.242G>A
n.830G>A
c.654G>A (p.Gln218=)
 gnomAD v4
4g.6291930G>CCA356172224WFS1c.645G>C (p.Gln215His)
c.622G>C
c.396G>C (p.Gln132His)
c.444G>C (p.Gln148His)
c.242G>C
n.830G>C
c.654G>C (p.Gln218His)
4g.6291930G>TCA356172225WFS1c.645G>T (p.Gln215His)
c.622G>T
c.396G>T (p.Gln132His)
c.444G>T (p.Gln148His)
c.242G>T
n.830G>T
c.654G>T (p.Gln218His)
 gnomAD v4
4g.6291931C>ACA356172226WFS1c.646C>A (p.Pro216Thr)
c.623C>A
c.397C>A (p.Pro133Thr)
c.445C>A (p.Pro149Thr)
c.243C>A
n.831C>A
c.655C>A (p.Pro219Thr)
 gnomAD v4
4g.6291931C>GCA356172227WFS1c.646C>G (p.Pro216Ala)
c.623C>G
c.397C>G (p.Pro133Ala)
c.445C>G (p.Pro149Ala)
c.243C>G
n.831C>G
c.655C>G (p.Pro219Ala)
4g.6291931C>TCA356172228WFS1c.646C>T (p.Pro216Ser)
c.623C>T
c.397C>T (p.Pro133Ser)
c.445C>T (p.Pro149Ser)
c.243C>T
n.831C>T
c.655C>T (p.Pro219Ser)
 dbSNP gnomAD v4
4g.6291932C>ACA356172229WFS1c.647C>A (p.Pro216Gln)
c.624C>A
c.398C>A (p.Pro133Gln)
c.446C>A (p.Pro149Gln)
c.244C>A
n.832C>A
c.656C>A (p.Pro219Gln)
4g.6291932C=CA1435768950WFS1c.647C= (p.Pro216=)
c.624C=
c.398C= (p.Pro133=)
c.446C= (p.Pro149=)
c.244C=
n.832C=
c.656C= (p.Pro219=)
4g.6291932C>GCA2838986WFS1c.647C>G (p.Pro216Arg)
c.624C>G
c.398C>G (p.Pro133Arg)
c.446C>G (p.Pro149Arg)
c.244C>G
n.832C>G
c.656C>G (p.Pro219Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291932C>TCA356172230WFS1c.647C>T (p.Pro216Leu)
c.624C>T
c.398C>T (p.Pro133Leu)
c.446C>T (p.Pro149Leu)
c.244C>T
n.832C>T
c.656C>T (p.Pro219Leu)
 dbSNP gnomAD v3 gnomAD v4
4g.6291933A>CCA438211047WFS1c.648A>C (p.Pro216=)
c.625A>C
c.399A>C (p.Pro133=)
c.447A>C (p.Pro149=)
c.245A>C
n.833A>C
c.657A>C (p.Pro219=)
4g.6291933A>GCA438211048WFS1c.648A>G (p.Pro216=)
c.625A>G
c.399A>G (p.Pro133=)
c.447A>G (p.Pro149=)
c.245A>G
n.833A>G
c.657A>G (p.Pro219=)
4g.6291933A>TCA438211049WFS1c.648A>T (p.Pro216=)
c.625A>T
c.399A>T (p.Pro133=)
c.447A>T (p.Pro149=)
c.245A>T
n.833A>T
c.657A>T (p.Pro219=)
4g.6291934G>ACA356172231WFS1c.649G>A (p.Gly217Ser)
c.626G>A
c.400G>A (p.Gly134Ser)
c.448G>A (p.Gly150Ser)
c.246G>A
n.834G>A
c.658G>A (p.Gly220Ser)
4g.6291934G>CCA356172233WFS1c.649G>C (p.Gly217Arg)
c.626G>C
c.400G>C (p.Gly134Arg)
c.448G>C (p.Gly150Arg)
c.246G>C
n.834G>C
c.658G>C (p.Gly220Arg)
4g.6291934G>TCA356172232WFS1c.649G>T (p.Gly217Cys)
c.626G>T
c.400G>T (p.Gly134Cys)
c.448G>T (p.Gly150Cys)
c.246G>T
n.834G>T
c.658G>T (p.Gly220Cys)
 gnomAD v4
4g.6291935G>ACA356172234WFS1c.650G>A (p.Gly217Asp)
c.627G>A
c.401G>A (p.Gly134Asp)
c.449G>A (p.Gly150Asp)
c.247G>A
n.835G>A
c.659G>A (p.Gly220Asp)
4g.6291935G>CCA356172235WFS1c.650G>C (p.Gly217Ala)
c.627G>C
c.401G>C (p.Gly134Ala)
c.449G>C (p.Gly150Ala)
c.247G>C
n.835G>C
c.659G>C (p.Gly220Ala)
4g.6291935G=CA1435768951WFS1c.650G= (p.Gly217=)
c.627G=
c.401G= (p.Gly134=)
c.449G= (p.Gly150=)
c.247G=
n.835G=
c.659G= (p.Gly220=)
4g.6291935G>TCA356172236WFS1c.650G>T (p.Gly217Val)
c.627G>T
c.401G>T (p.Gly134Val)
c.449G>T (p.Gly150Val)
c.247G>T
n.835G>T
c.659G>T (p.Gly220Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6291936C>ACA438211053WFS1c.651C>A (p.Gly217=)
c.628C>A
c.402C>A (p.Gly134=)
c.450C>A (p.Gly150=)
c.248C>A
n.836C>A
c.660C>A (p.Gly220=)
 dbSNP gnomAD v2 gnomAD v4
4g.6291936C=CA1435768952WFS1c.651C= (p.Gly217=)
c.628C=
c.402C= (p.Gly134=)
c.450C= (p.Gly150=)
c.248C=
n.836C=
c.660C= (p.Gly220=)
4g.6291936C>GCA438211052WFS1c.651C>G (p.Gly217=)
c.628C>G
c.402C>G (p.Gly134=)
c.450C>G (p.Gly150=)
c.248C>G
n.836C>G
c.660C>G (p.Gly220=)
4g.6291936C>TCA438211051WFS1c.651C>T (p.Gly217=)
c.628C>T
c.402C>T (p.Gly134=)
c.450C>T (p.Gly150=)
c.248C>T
n.836C>T
c.660C>T (p.Gly220=)
4g.6291939delCA2586973598WFS1c.654del (p.Val219CysfsTer?)
c.631del
c.405del (p.Val136CysfsTer?)
c.453del (p.Val152CysfsTer?)
c.251del
n.839del
c.663del (p.Val222CysfsTer?)
4g.6291937C>ACA356172237WFS1c.652C>A (p.Pro218Thr)
c.629C>A
c.403C>A (p.Pro135Thr)
c.451C>A (p.Pro151Thr)
c.249C>A
n.837C>A
c.661C>A (p.Pro221Thr)
4g.6291937C=CA1435768953WFS1c.652C= (p.Pro218=)
c.629C=
c.403C= (p.Pro135=)
c.451C= (p.Pro151=)
c.249C=
n.837C=
c.661C= (p.Pro221=)
4g.6291937C>GCA356172238WFS1c.652C>G (p.Pro218Ala)
c.629C>G
c.403C>G (p.Pro135Ala)
c.451C>G (p.Pro151Ala)
c.249C>G
n.837C>G
c.661C>G (p.Pro221Ala)
 gnomAD v4
4g.6291937C>TCA356172239WFS1c.652C>T (p.Pro218Ser)
c.629C>T
c.403C>T (p.Pro135Ser)
c.451C>T (p.Pro151Ser)
c.249C>T
n.837C>T
c.661C>T (p.Pro221Ser)
 dbSNP gnomAD v2 gnomAD v4
4g.6291938C>ACA356172240WFS1c.653C>A (p.Pro218His)
c.630C>A
c.404C>A (p.Pro135His)
c.452C>A (p.Pro151His)
c.250C>A
n.838C>A
c.662C>A (p.Pro221His)
 dbSNP gnomAD v2 gnomAD v4
4g.6291938C=CA1435768954WFS1c.653C= (p.Pro218=)
c.630C=
c.404C= (p.Pro135=)
c.452C= (p.Pro151=)
c.250C=
n.838C=
c.662C= (p.Pro221=)
4g.6291938C>GCA356172241WFS1c.653C>G (p.Pro218Arg)
c.630C>G
c.404C>G (p.Pro135Arg)
c.452C>G (p.Pro151Arg)
c.250C>G
n.838C>G
c.662C>G (p.Pro221Arg)
4g.6291938C>TCA356172242WFS1c.653C>T (p.Pro218Leu)
c.630C>T
c.404C>T (p.Pro135Leu)
c.452C>T (p.Pro151Leu)
c.250C>T
n.838C>T
c.662C>T (p.Pro221Leu)
 dbSNP gnomAD v2 COSMIC
4g.6291939C>ACA438211054WFS1c.654C>A (p.Pro218=)
c.631C>A
c.405C>A (p.Pro135=)
c.453C>A (p.Pro151=)
c.251C>A
n.839C>A
c.663C>A (p.Pro221=)
 gnomAD v4
4g.6291939C=CA1435768955WFS1c.654C= (p.Pro218=)
c.631C=
c.405C= (p.Pro135=)
c.453C= (p.Pro151=)
c.251C=
n.839C=
c.663C= (p.Pro221=)
4g.6291939C>GCA438211055WFS1c.654C>G (p.Pro218=)
c.631C>G
c.405C>G (p.Pro135=)
c.453C>G (p.Pro151=)
c.251C>G
n.839C>G
c.663C>G (p.Pro221=)
 ClinVar dbSNP
4g.6291939C>TCA183810WFS1c.654C>T (p.Pro218=)
c.631C>T
c.405C>T (p.Pro135=)
c.453C>T (p.Pro151=)
c.251C>T
n.839C>T
c.663C>T (p.Pro221=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291940G>ACA2838987WFS1c.655G>A (p.Val219Met)
c.632G>A
c.406G>A (p.Val136Met)
c.454G>A (p.Val152Met)
c.252G>A
n.840G>A
c.664G>A (p.Val222Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291940G>CCA356172244WFS1c.655G>C (p.Val219Leu)
c.632G>C
c.406G>C (p.Val136Leu)
c.454G>C (p.Val152Leu)
c.252G>C
n.840G>C
c.664G>C (p.Val222Leu)
 dbSNP gnomAD v3 gnomAD v4
4g.6291940G=CA1435768956WFS1c.655G= (p.Val219=)
c.632G=
c.406G= (p.Val136=)
c.454G= (p.Val152=)
c.252G=
n.840G=
c.664G= (p.Val222=)
4g.6291940G>TCA356172243WFS1c.655G>T (p.Val219Leu)
c.632G>T
c.406G>T (p.Val136Leu)
c.454G>T (p.Val152Leu)
c.252G>T
n.840G>T
c.664G>T (p.Val222Leu)
4g.6291941T>ACA356172245WFS1c.656T>A (p.Val219Glu)
c.633T>A
c.407T>A (p.Val136Glu)
c.455T>A (p.Val152Glu)
c.253T>A
n.841T>A
c.665T>A (p.Val222Glu)
4g.6291941T>CCA2838988WFS1c.656T>C (p.Val219Ala)
c.633T>C
c.407T>C (p.Val136Ala)
c.455T>C (p.Val152Ala)
c.253T>C
n.841T>C
c.665T>C (p.Val222Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291941T>GCA356172246WFS1c.656T>G (p.Val219Gly)
c.633T>G
c.407T>G (p.Val136Gly)
c.455T>G (p.Val152Gly)
c.253T>G
n.841T>G
c.665T>G (p.Val222Gly)
4g.6291941T=CA1435768957WFS1c.656T= (p.Val219=)
c.633T=
c.407T= (p.Val136=)
c.455T= (p.Val152=)
c.253T=
n.841T=
c.665T= (p.Val222=)
4g.6291942G>ACA438211056WFS1c.657G>A (p.Val219=)
c.634G>A
c.408G>A (p.Val136=)
c.456G>A (p.Val152=)
c.254G>A
n.842G>A
c.666G>A (p.Val222=)
 dbSNP
4g.6291942G>CCA438211058WFS1c.657G>C (p.Val219=)
c.634G>C
c.408G>C (p.Val136=)
c.456G>C (p.Val152=)
c.254G>C
n.842G>C
c.666G>C (p.Val222=)
4g.6291942G=CA1435768958WFS1c.657G= (p.Val219=)
c.634G=
c.408G= (p.Val136=)
c.456G= (p.Val152=)
c.254G=
n.842G=
c.666G= (p.Val222=)
4g.6291942G>TCA438211057WFS1c.657G>T (p.Val219=)
c.634G>T
c.408G>T (p.Val136=)
c.456G>T (p.Val152=)
c.254G>T
n.842G>T
c.666G>T (p.Val222=)
 gnomAD v4
4g.6291943C>ACA356172247WFS1c.658C>A (p.Pro220Thr)
c.635C>A
c.409C>A (p.Pro137Thr)
c.457C>A (p.Pro153Thr)
c.255C>A
n.843C>A
c.667C>A (p.Pro223Thr)
4g.6291943C>GCA356172248WFS1c.658C>G (p.Pro220Ala)
c.635C>G
c.409C>G (p.Pro137Ala)
c.457C>G (p.Pro153Ala)
c.255C>G
n.843C>G
c.667C>G (p.Pro223Ala)
4g.6291943C>TCA356172249WFS1c.658C>T (p.Pro220Ser)
c.635C>T
c.409C>T (p.Pro137Ser)
c.457C>T (p.Pro153Ser)
c.255C>T
n.843C>T
c.667C>T (p.Pro223Ser)
 gnomAD v4
4g.6291944C>ACA356172250WFS1c.659C>A (p.Pro220His)
c.636C>A
c.410C>A (p.Pro137His)
c.458C>A (p.Pro153His)
c.256C>A
n.844C>A
c.668C>A (p.Pro223His)
4g.6291944C>GCA356172251WFS1c.659C>G (p.Pro220Arg)
c.636C>G
c.410C>G (p.Pro137Arg)
c.458C>G (p.Pro153Arg)
c.256C>G
n.844C>G
c.668C>G (p.Pro223Arg)
4g.6291944C>TCA356172252WFS1c.659C>T (p.Pro220Leu)
c.636C>T
c.410C>T (p.Pro137Leu)
c.458C>T (p.Pro153Leu)
c.256C>T
n.844C>T
c.668C>T (p.Pro223Leu)
 gnomAD v4
4g.6291945C>ACA438211059WFS1c.660C>A (p.Pro220=)
c.637C>A
c.411C>A (p.Pro137=)
c.459C>A (p.Pro153=)
c.257C>A
n.845C>A
c.669C>A (p.Pro223=)
 gnomAD v4
4g.6291945C=CA1435768959WFS1c.660C= (p.Pro220=)
c.637C=
c.411C= (p.Pro137=)
c.459C= (p.Pro153=)
c.257C=
n.845C=
c.669C= (p.Pro223=)
4g.6291945C>GCA438211060WFS1c.660C>G (p.Pro220=)
c.637C>G
c.411C>G (p.Pro137=)
c.459C>G (p.Pro153=)
c.257C>G
n.845C>G
c.669C>G (p.Pro223=)
4g.6291945C>TCA2838989WFS1c.660C>T (p.Pro220=)
c.637C>T
c.411C>T (p.Pro137=)
c.459C>T (p.Pro153=)
c.257C>T
n.845C>T
c.669C>T (p.Pro223=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6291946A>CCA356172253WFS1c.661A>C (p.Lys221Gln)
c.638A>C
c.412A>C (p.Lys138Gln)
c.460A>C (p.Lys154Gln)
c.258A>C
n.846A>C
c.670A>C (p.Lys224Gln)
4g.6291946A>GCA356172254WFS1c.661A>G (p.Lys221Glu)
c.638A>G
c.412A>G (p.Lys138Glu)
c.460A>G (p.Lys154Glu)
c.258A>G
n.846A>G
c.670A>G (p.Lys224Glu)
4g.6291946A>TCA356172255WFS1c.661A>T (p.Lys221Ter)
c.638A>T
c.412A>T (p.Lys138Ter)
c.460A>T (p.Lys154Ter)
c.258A>T
n.846A>T
c.670A>T (p.Lys224Ter)
 gnomAD v4
4g.6291947A=CA1435768960WFS1c.662A= (p.Lys221=)
c.639A=
c.413A= (p.Lys138=)
c.461A= (p.Lys154=)
c.259A=
n.847A=
c.671A= (p.Lys224=)
4g.6291947A>CCA356172257WFS1c.662A>C (p.Lys221Thr)
c.639A>C
c.413A>C (p.Lys138Thr)
c.461A>C (p.Lys154Thr)
c.259A>C
n.847A>C
c.671A>C (p.Lys224Thr)
 ClinVar gnomAD v4
4g.6291947A>GCA2838990WFS1c.662A>G (p.Lys221Arg)
c.639A>G
c.413A>G (p.Lys138Arg)
c.461A>G (p.Lys154Arg)
c.259A>G
n.847A>G
c.671A>G (p.Lys224Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291947A>TCA356172256WFS1c.662A>T (p.Lys221Met)
c.639A>T
c.413A>T (p.Lys138Met)
c.461A>T (p.Lys154Met)
c.259A>T
n.847A>T
c.671A>T (p.Lys224Met)
4g.6291948G>ACA438211061WFS1c.663G>A (p.Lys221=)
c.640G>A
c.414G>A (p.Lys138=)
c.462G>A (p.Lys154=)
c.260G>A
n.848G>A
c.672G>A (p.Lys224=)
4g.6291948G>CCA356172258WFS1c.663G>C (p.Lys221Asn)
c.640G>C
c.414G>C (p.Lys138Asn)
c.462G>C (p.Lys154Asn)
c.260G>C
n.848G>C
c.672G>C (p.Lys224Asn)
 ClinVar dbSNP gnomAD v4
4g.6291948G>TCA356172259WFS1c.663G>T (p.Lys221Asn)
c.640G>T
c.414G>T (p.Lys138Asn)
c.462G>T (p.Lys154Asn)
c.260G>T
n.848G>T
c.672G>T (p.Lys224Asn)
4g.6291949T>ACA356172260WFS1c.664T>A (p.Ser222Thr)
c.641T>A
c.415T>A (p.Ser139Thr)
c.463T>A (p.Ser155Thr)
c.261T>A
n.849T>A
c.673T>A (p.Ser225Thr)
4g.6291949T>CCA356172261WFS1c.664T>C (p.Ser222Pro)
c.641T>C
c.415T>C (p.Ser139Pro)
c.463T>C (p.Ser155Pro)
c.261T>C
n.849T>C
c.673T>C (p.Ser225Pro)
4g.6291949T>GCA356172262WFS1c.664T>G (p.Ser222Ala)
c.641T>G
c.415T>G (p.Ser139Ala)
c.463T>G (p.Ser155Ala)
c.261T>G
n.849T>G
c.673T>G (p.Ser225Ala)
4g.6291950C>ACA356172263WFS1c.665C>A (p.Ser222Tyr)
c.642C>A
c.416C>A (p.Ser139Tyr)
c.464C>A (p.Ser155Tyr)
c.262C>A
n.850C>A
c.674C>A (p.Ser225Tyr)
 ClinVar dbSNP gnomAD v4
4g.6291950C=CA1435768961WFS1c.665C= (p.Ser222=)
c.642C=
c.416C= (p.Ser139=)
c.464C= (p.Ser155=)
c.262C=
n.850C=
c.674C= (p.Ser225=)
4g.6291950C>GCA356172264WFS1c.665C>G (p.Ser222Cys)
c.642C>G
c.416C>G (p.Ser139Cys)
c.464C>G (p.Ser155Cys)
c.262C>G
n.850C>G
c.674C>G (p.Ser225Cys)
4g.6291950C>TCA356172265WFS1c.665C>T (p.Ser222Phe)
c.642C>T
c.416C>T (p.Ser139Phe)
c.464C>T (p.Ser155Phe)
c.262C>T
n.850C>T
c.674C>T (p.Ser225Phe)
 COSMIC
4g.6291950_6291951delinsTTCA645523665WFS1c.665_666delinsTT (p.Ser222Phe)
c.642_643delinsTT
c.416_417delinsTT (p.Ser139Phe)
c.464_465delinsTT (p.Ser155Phe)
c.262_263delinsTT
n.850_851delinsTT
c.674_675delinsTT (p.Ser225Phe)
 COSMIC
4g.6291951C>ACA438211062WFS1c.666C>A (p.Ser222=)
c.643C>A
c.417C>A (p.Ser139=)
c.465C>A (p.Ser155=)
c.263C>A
n.851C>A
c.675C>A (p.Ser225=)
 gnomAD v4
4g.6291951C=CA1435768962WFS1c.666C= (p.Ser222=)
c.643C=
c.417C= (p.Ser139=)
c.465C= (p.Ser155=)
c.263C=
n.851C=
c.675C= (p.Ser225=)
4g.6291951C>GCA438211063WFS1c.666C>G (p.Ser222=)
c.643C>G
c.417C>G (p.Ser139=)
c.465C>G (p.Ser155=)
c.263C>G
n.851C>G
c.675C>G (p.Ser225=)
4g.6291951C>TCA91794669WFS1c.666C>T (p.Ser222=)
c.643C>T
c.417C>T (p.Ser139=)
c.465C>T (p.Ser155=)
c.263C>T
n.851C>T
c.675C>T (p.Ser225=)
 dbSNP gnomAD v2 gnomAD v4
4g.6291952C>ACA16609251WFS1c.667C>A (p.Leu223Met)
c.644C>A
c.418C>A (p.Leu140Met)
c.466C>A (p.Leu156Met)
c.264C>A
n.852C>A
c.676C>A (p.Leu226Met)
 ClinVar dbSNP gnomAD v4
4g.6291952C=CA1435768963WFS1c.667C= (p.Leu223=)
c.644C=
c.418C= (p.Leu140=)
c.466C= (p.Leu156=)
c.264C=
n.852C=
c.676C= (p.Leu226=)
4g.6291952C>GCA356172266WFS1c.667C>G (p.Leu223Val)
c.644C>G
c.418C>G (p.Leu140Val)
c.466C>G (p.Leu156Val)
c.264C>G
n.852C>G
c.676C>G (p.Leu226Val)
4g.6291952C>TCA438211064WFS1c.667C>T (p.Leu223=)
c.644C>T
c.418C>T (p.Leu140=)
c.466C>T (p.Leu156=)
c.264C>T
n.852C>T
c.676C>T (p.Leu226=)
 ClinVar
4g.6291953T>ACA356172269WFS1c.668T>A (p.Leu223Gln)
c.645T>A
c.419T>A (p.Leu140Gln)
c.467T>A (p.Leu156Gln)
c.265T>A
n.853T>A
c.677T>A (p.Leu226Gln)
4g.6291953T>CCA356172268WFS1c.668T>C (p.Leu223Pro)
c.645T>C
c.419T>C (p.Leu140Pro)
c.467T>C (p.Leu156Pro)
c.265T>C
n.853T>C
c.677T>C (p.Leu226Pro)
 gnomAD v4
4g.6291953T>GCA356172267WFS1c.668T>G (p.Leu223Arg)
c.645T>G
c.419T>G (p.Leu140Arg)
c.467T>G (p.Leu156Arg)
c.265T>G
n.853T>G
c.677T>G (p.Leu226Arg)
4g.6291954G>ACA438211065WFS1c.669G>A (p.Leu223=)
c.646G>A
c.420G>A (p.Leu140=)
c.468G>A (p.Leu156=)
c.266G>A
n.854G>A
c.678G>A (p.Leu226=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6291954G>CCA438211066WFS1c.669G>C (p.Leu223=)
c.646G>C
c.420G>C (p.Leu140=)
c.468G>C (p.Leu156=)
c.266G>C
n.854G>C
c.678G>C (p.Leu226=)
4g.6291954G=CA1435768964WFS1c.669G= (p.Leu223=)
c.646G=
c.420G= (p.Leu140=)
c.468G= (p.Leu156=)
c.266G=
n.854G=
c.678G= (p.Leu226=)
4g.6291954G>TCA438211067WFS1c.669G>T (p.Leu223=)
c.646G>T
c.420G>T (p.Leu140=)
c.468G>T (p.Leu156=)
c.266G>T
n.854G>T
c.678G>T (p.Leu226=)
 gnomAD v4
4g.6291955C>ACA356172270WFS1c.670C>A (p.Gln224Lys)
c.647C>A
c.421C>A (p.Gln141Lys)
c.469C>A (p.Gln157Lys)
c.267C>A
n.855C>A
c.679C>A (p.Gln227Lys)
 dbSNP gnomAD v4
4g.6291955C=CA1435768965WFS1c.670C= (p.Gln224=)
c.647C=
c.421C= (p.Gln141=)
c.469C= (p.Gln157=)
c.267C=
n.855C=
c.679C= (p.Gln227=)
4g.6291955C>GCA356172272WFS1c.670C>G (p.Gln224Glu)
c.647C>G
c.421C>G (p.Gln141Glu)
c.469C>G (p.Gln157Glu)
c.267C>G
n.855C>G
c.679C>G (p.Gln227Glu)
4g.6291955C>TCA356172271WFS1c.670C>T (p.Gln224Ter)
c.647C>T
c.421C>T (p.Gln141Ter)
c.469C>T (p.Gln157Ter)
c.267C>T
n.855C>T
c.679C>T (p.Gln227Ter)
 gnomAD v4
4g.6291956A=CA1435768966WFS1c.671A= (p.Gln224=)
c.648A=
c.422A= (p.Gln141=)
c.470A= (p.Gln157=)
c.268A=
n.856A=
c.680A= (p.Gln227=)
4g.6291956A>CCA356172273WFS1c.671A>C (p.Gln224Pro)
c.648A>C
c.422A>C (p.Gln141Pro)
c.470A>C (p.Gln157Pro)
c.268A>C
n.856A>C
c.680A>C (p.Gln227Pro)
4g.6291956A>GCA356172275WFS1c.671A>G (p.Gln224Arg)
c.648A>G
c.422A>G (p.Gln141Arg)
c.470A>G (p.Gln157Arg)
c.268A>G
n.856A>G
c.680A>G (p.Gln227Arg)
 dbSNP gnomAD v2
4g.6291956A>TCA356172274WFS1c.671A>T (p.Gln224Leu)
c.648A>T
c.422A>T (p.Gln141Leu)
c.470A>T (p.Gln157Leu)
c.268A>T
n.856A>T
c.680A>T (p.Gln227Leu)
4g.6291957G>ACA438211069WFS1c.672G>A (p.Gln224=)
c.649G>A
c.423G>A (p.Gln141=)
c.471G>A (p.Gln157=)
c.269G>A
n.857G>A
c.681G>A (p.Gln227=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6291957G>CCA356172276WFS1c.672G>C (p.Gln224His)
c.649G>C
c.423G>C (p.Gln141His)
c.471G>C (p.Gln157His)
c.269G>C
n.857G>C
c.681G>C (p.Gln227His)
4g.6291957G=CA1435768967WFS1c.672G= (p.Gln224=)
c.649G=
c.423G= (p.Gln141=)
c.471G= (p.Gln157=)
c.269G=
n.857G=
c.681G= (p.Gln227=)
4g.6291957G>TCA356172277WFS1c.672G>T (p.Gln224His)
c.649G>T
c.423G>T (p.Gln141His)
c.471G>T (p.Gln157His)
c.269G>T
n.857G>T
c.681G>T (p.Gln227His)
 gnomAD v4
4g.6291958A=CA1435768968WFS1c.673A= (p.Lys225=)
c.650A=
c.424A= (p.Lys142=)
c.472A= (p.Lys158=)
c.270A=
n.858A=
c.682A= (p.Lys228=)
4g.6291958A>CCA356172278WFS1c.673A>C (p.Lys225Gln)
c.650A>C
c.424A>C (p.Lys142Gln)
c.472A>C (p.Lys158Gln)
c.270A>C
n.858A>C
c.682A>C (p.Lys228Gln)
 dbSNP
4g.6291958A>GCA356172279WFS1c.673A>G (p.Lys225Glu)
c.650A>G
c.424A>G (p.Lys142Glu)
c.472A>G (p.Lys158Glu)
c.270A>G
n.858A>G
c.682A>G (p.Lys228Glu)
 ClinVar dbSNP
4g.6291958A>TCA356172280WFS1c.673A>T (p.Lys225Ter)
c.650A>T
c.424A>T (p.Lys142Ter)
c.472A>T (p.Lys158Ter)
c.270A>T
n.858A>T
c.682A>T (p.Lys228Ter)
4g.6291959A>CCA356172281WFS1c.674A>C (p.Lys225Thr)
c.651A>C
c.425A>C (p.Lys142Thr)
c.473A>C (p.Lys158Thr)
c.271A>C
n.859A>C
c.683A>C (p.Lys228Thr)
4g.6291959A>GCA356172282WFS1c.674A>G (p.Lys225Arg)
c.651A>G
c.425A>G (p.Lys142Arg)
c.473A>G (p.Lys158Arg)
c.271A>G
n.859A>G
c.683A>G (p.Lys228Arg)
4g.6291959A>TCA356172283WFS1c.674A>T (p.Lys225Met)
c.651A>T
c.425A>T (p.Lys142Met)
c.473A>T (p.Lys158Met)
c.271A>T
n.859A>T
c.683A>T (p.Lys228Met)
4g.6291960G>ACA2838991WFS1c.675G>A (p.Lys225=)
c.652G>A
c.426G>A (p.Lys142=)
c.474G>A (p.Lys158=)
c.272G>A
n.860G>A
c.684G>A (p.Lys228=)
 dbSNP ExAC gnomAD v2
4g.6291960G>CCA356172284WFS1c.675G>C (p.Lys225Asn)
c.652G>C
c.426G>C (p.Lys142Asn)
c.474G>C (p.Lys158Asn)
c.272G>C
n.860G>C
c.684G>C (p.Lys228Asn)
4g.6291960G=CA1435768969WFS1c.675G= (p.Lys225=)
c.652G=
c.426G= (p.Lys142=)
c.474G= (p.Lys158=)
c.272G=
n.860G=
c.684G= (p.Lys228=)
4g.6291960G>TCA356172285WFS1c.675G>T (p.Lys225Asn)
c.652G>T
c.426G>T (p.Lys142Asn)
c.474G>T (p.Lys158Asn)
c.272G>T
n.860G>T
c.684G>T (p.Lys228Asn)
 gnomAD v4
4g.6291961C>ACA356172286WFS1c.676C>A (p.Gln226Lys)
c.653C>A
c.427C>A (p.Gln143Lys)
c.475C>A (p.Gln159Lys)
c.273C>A
n.861C>A
c.685C>A (p.Gln229Lys)
 gnomAD v4
4g.6291961C=CA1435768970WFS1c.676C= (p.Gln226=)
c.653C=
c.427C= (p.Gln143=)
c.475C= (p.Gln159=)
c.273C=
n.861C=
c.685C= (p.Gln229=)
4g.6291961C>GCA356172287WFS1c.676C>G (p.Gln226Glu)
c.653C>G
c.427C>G (p.Gln143Glu)
c.475C>G (p.Gln159Glu)
c.273C>G
n.861C>G
c.685C>G (p.Gln229Glu)
4g.6291961C>TCA253192WFS1c.676C>T (p.Gln226Ter)
c.653C>T
c.427C>T (p.Gln143Ter)
c.475C>T (p.Gln159Ter)
c.273C>T
n.861C>T
c.685C>T (p.Gln229Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6291962A>CCA356172288WFS1c.677A>C (p.Gln226Pro)
c.654A>C
c.428A>C (p.Gln143Pro)
c.476A>C (p.Gln159Pro)
c.274A>C
n.862A>C
c.686A>C (p.Gln229Pro)
4g.6291962A>GCA356172290WFS1c.677A>G (p.Gln226Arg)
c.654A>G
c.428A>G (p.Gln143Arg)
c.476A>G (p.Gln159Arg)
c.274A>G
n.862A>G
c.686A>G (p.Gln229Arg)
4g.6291962A>TCA356172289WFS1c.677A>T (p.Gln226Leu)
c.654A>T
c.428A>T (p.Gln143Leu)
c.476A>T (p.Gln159Leu)
c.274A>T
n.862A>T
c.686A>T (p.Gln229Leu)
4g.6291963G>ACA438211071WFS1c.678G>A (p.Gln226=)
c.655G>A
c.429G>A (p.Gln143=)
c.477G>A (p.Gln159=)
c.275G>A
n.863G>A
c.687G>A (p.Gln229=)
4g.6291963G>CCA356172291WFS1c.678G>C (p.Gln226His)
c.655G>C
c.429G>C (p.Gln143His)
c.477G>C (p.Gln159His)
c.275G>C
n.863G>C
c.687G>C (p.Gln229His)
4g.6291963G>TCA356172292WFS1c.678G>T (p.Gln226His)
c.655G>T
c.429G>T (p.Gln143His)
c.477G>T (p.Gln159His)
c.275G>T
n.863G>T
c.687G>T (p.Gln229His)
4g.6291964A>CCA438211072WFS1c.679A>C (p.Arg227=)
c.656A>C
c.430A>C (p.Arg144=)
c.478A>C (p.Arg160=)
c.276A>C
n.864A>C
c.688A>C (p.Arg230=)
4g.6291964A>GCA356172293WFS1c.679A>G (p.Arg227Gly)
c.656A>G
c.430A>G (p.Arg144Gly)
c.478A>G (p.Arg160Gly)
c.276A>G
n.864A>G
c.688A>G (p.Arg230Gly)
 gnomAD v4
4g.6291964A>TCA356172294WFS1c.679A>T (p.Arg227Trp)
c.656A>T
c.430A>T (p.Arg144Trp)
c.478A>T (p.Arg160Trp)
c.276A>T
n.864A>T
c.688A>T (p.Arg230Trp)
4g.6291965G>ACA356172295WFS1c.680G>A (p.Arg227Lys)
c.657G>A
c.431G>A (p.Arg144Lys)
c.479G>A (p.Arg160Lys)
c.277G>A
n.865G>A
c.689G>A (p.Arg230Lys)
4g.6291965G>CCA356172296WFS1c.680G>C (p.Arg227Thr)
c.657G>C
c.431G>C (p.Arg144Thr)
c.479G>C (p.Arg160Thr)
c.277G>C
n.865G>C
c.689G>C (p.Arg230Thr)
4g.6291965G>TCA356172297WFS1c.680G>T (p.Arg227Met)
c.657G>T
c.431G>T (p.Arg144Met)
c.479G>T (p.Arg160Met)
c.277G>T
n.865G>T
c.689G>T (p.Arg230Met)
4g.6291966G>ACA438211073WFS1c.681G>A (p.Arg227=)
c.658G>A
c.432G>A (p.Arg144=)
c.480G>A (p.Arg160=)
c.278G>A
n.866G>A
c.690G>A (p.Arg230=)
4g.6291966G>CCA356172298WFS1c.681G>C (p.Arg227Ser)
c.658G>C
c.432G>C (p.Arg144Ser)
c.480G>C (p.Arg160Ser)
c.278G>C
n.866G>C
c.690G>C (p.Arg230Ser)
4g.6291966G>TCA356172299WFS1c.681G>T (p.Arg227Ser)
c.658G>T
c.432G>T (p.Arg144Ser)
c.480G>T (p.Arg160Ser)
c.278G>T
n.866G>T
c.690G>T (p.Arg230Ser)
 gnomAD v4
4g.6291967C>ACA356172300WFS1c.682C>A (p.Arg228Ser)
c.659C>A
c.433C>A (p.Arg145Ser)
c.481C>A (p.Arg161Ser)
c.279C>A
n.867C>A
c.691C>A (p.Arg231Ser)
 gnomAD v4
4g.6291967C=CA1435768971WFS1c.682C= (p.Arg228=)
c.659C=
c.433C= (p.Arg145=)
c.481C= (p.Arg161=)
c.279C=
n.867C=
c.691C= (p.Arg231=)
4g.6291967C>GCA356172301WFS1c.682C>G (p.Arg228Gly)
c.659C>G
c.433C>G (p.Arg145Gly)
c.481C>G (p.Arg161Gly)
c.279C>G
n.867C>G
c.691C>G (p.Arg231Gly)
4g.6291967C>TCA2838992WFS1c.682C>T (p.Arg228Cys)
c.659C>T
c.433C>T (p.Arg145Cys)
c.481C>T (p.Arg161Cys)
c.279C>T
n.867C>T
c.691C>T (p.Arg231Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6291968G>ACA246711WFS1c.683G>A (p.Arg228His)
c.660G>A
c.434G>A (p.Arg145His)
c.482G>A (p.Arg161His)
c.280G>A
n.868G>A
c.692G>A (p.Arg231His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291968G>CCA356172302WFS1c.683G>C (p.Arg228Pro)
c.660G>C
c.434G>C (p.Arg145Pro)
c.482G>C (p.Arg161Pro)
c.280G>C
n.868G>C
c.692G>C (p.Arg231Pro)
4g.6291968G=CA1435768972WFS1c.683G= (p.Arg228=)
c.660G=
c.434G= (p.Arg145=)
c.482G= (p.Arg161=)
c.280G=
n.868G=
c.692G= (p.Arg231=)
4g.6291968G>TCA356172303WFS1c.683G>T (p.Arg228Leu)
c.660G>T
c.434G>T (p.Arg145Leu)
c.482G>T (p.Arg161Leu)
c.280G>T
n.868G>T
c.692G>T (p.Arg231Leu)
 dbSNP gnomAD v2 gnomAD v4
4g.6291968_6291969delinsAACA913185074WFS1c.683_684delinsAA (p.Arg228Gln)
c.660_661delinsAA
c.434_435delinsAA (p.Arg145Gln)
c.482_483delinsAA (p.Arg161Gln)
c.280_281delinsAA
n.868_869delinsAA
c.692_693delinsAA (p.Arg231Gln)
4g.6291968_6291969delinsAGCA2573138322WFS1c.683_684delinsAG (p.Arg228Gln)
c.660_661delinsAG
c.434_435delinsAG (p.Arg145Gln)
c.482_483delinsAG (p.Arg161Gln)
c.280_281delinsAG
n.868_869delinsAG
c.692_693delinsAG (p.Arg231Gln)
 ClinVar dbSNP
4g.6291968_6291969delinsTGCA2695199362WFS1c.683_684delinsTG (p.Arg228Leu)
c.660_661delinsTG
c.434_435delinsTG (p.Arg145Leu)
c.482_483delinsTG (p.Arg161Leu)
c.280_281delinsTG
n.868_869delinsTG
c.692_693delinsTG (p.Arg231Leu)
 ClinVar
4g.6291969C>ACA438211074WFS1c.684C>A (p.Arg228=)
c.661C>A
c.435C>A (p.Arg145=)
c.483C>A (p.Arg161=)
c.281C>A
n.869C>A
c.693C>A (p.Arg231=)
 dbSNP gnomAD v4
4g.6291969C=CA1435768973WFS1c.684C= (p.Arg228=)
c.661C=
c.435C= (p.Arg145=)
c.483C= (p.Arg161=)
c.281C=
n.869C=
c.693C= (p.Arg231=)
4g.6291969C>GCA136359WFS1c.684C>G (p.Arg228=)
c.661C>G
c.435C>G (p.Arg145=)
c.483C>G (p.Arg161=)
c.281C>G
n.869C>G
c.693C>G (p.Arg231=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291969C>TCA438211075WFS1c.684C>T (p.Arg228=)
c.661C>T
c.435C>T (p.Arg145=)
c.483C>T (p.Arg161=)
c.281C>T
n.869C>T
c.693C>T (p.Arg231=)
 dbSNP gnomAD v4
4g.6291970A=CA1435768974WFS1c.685A= (p.Met229=)
c.662A=
c.436A= (p.Met146=)
c.484A= (p.Met162=)
c.282A=
n.870A=
c.694A= (p.Met232=)
4g.6291970A>CCA356172304WFS1c.685A>C (p.Met229Leu)
c.662A>C
c.436A>C (p.Met146Leu)
c.484A>C (p.Met162Leu)
c.282A>C
n.870A>C
c.694A>C (p.Met232Leu)
4g.6291970A>GCA356172305WFS1c.685A>G (p.Met229Val)
c.662A>G
c.436A>G (p.Met146Val)
c.484A>G (p.Met162Val)
c.282A>G
n.870A>G
c.694A>G (p.Met232Val)
 dbSNP gnomAD v2 gnomAD v4
4g.6291970A>TCA356172306WFS1c.685A>T (p.Met229Leu)
c.662A>T
c.436A>T (p.Met146Leu)
c.484A>T (p.Met162Leu)
c.282A>T
n.870A>T
c.694A>T (p.Met232Leu)
4g.6291971T>ACA356172307WFS1c.686T>A (p.Met229Lys)
c.663T>A
c.437T>A (p.Met146Lys)
c.485T>A (p.Met162Lys)
c.283T>A
n.871T>A
c.695T>A (p.Met232Lys)
4g.6291971T>CCA2838993WFS1c.686T>C (p.Met229Thr)
c.663T>C
c.437T>C (p.Met146Thr)
c.485T>C (p.Met162Thr)
c.283T>C
n.871T>C
c.695T>C (p.Met232Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291971T>GCA356172308WFS1c.686T>G (p.Met229Arg)
c.663T>G
c.437T>G (p.Met146Arg)
c.485T>G (p.Met162Arg)
c.283T>G
n.871T>G
c.695T>G (p.Met232Arg)
4g.6291971T=CA1435768975WFS1c.686T= (p.Met229=)
c.663T=
c.437T= (p.Met146=)
c.485T= (p.Met162=)
c.283T=
n.871T=
c.695T= (p.Met232=)
4g.6291972G>ACA356172309WFS1c.687G>A (p.Met229Ile)
c.664G>A
c.438G>A (p.Met146Ile)
c.486G>A (p.Met162Ile)
c.284G>A
n.872G>A
c.696G>A (p.Met232Ile)
 dbSNP gnomAD v3 gnomAD v4
4g.6291972G>CCA356172310WFS1c.687G>C (p.Met229Ile)
c.664G>C
c.438G>C (p.Met146Ile)
c.486G>C (p.Met162Ile)
c.284G>C
n.872G>C
c.696G>C (p.Met232Ile)
 dbSNP
4g.6291972G=CA1435768976WFS1c.687G= (p.Met229=)
c.664G=
c.438G= (p.Met146=)
c.486G= (p.Met162=)
c.284G=
n.872G=
c.696G= (p.Met232=)
4g.6291972G>TCA356172311WFS1c.687G>T (p.Met229Ile)
c.664G>T
c.438G>T (p.Met146Ile)
c.486G>T (p.Met162Ile)
c.284G>T
n.872G>T
c.696G>T (p.Met232Ile)
 dbSNP gnomAD v4
4g.6291973C>ACA356172312WFS1c.688C>A (p.Leu230Met)
c.665C>A
c.439C>A (p.Leu147Met)
c.487C>A (p.Leu163Met)
c.285C>A
n.873C>A
c.697C>A (p.Leu233Met)
 gnomAD v4
4g.6291973C>GCA356172313WFS1c.688C>G (p.Leu230Val)
c.665C>G
c.439C>G (p.Leu147Val)
c.487C>G (p.Leu163Val)
c.285C>G
n.873C>G
c.697C>G (p.Leu233Val)
4g.6291973C>TCA438211076WFS1c.688C>T (p.Leu230=)
c.665C>T
c.439C>T (p.Leu147=)
c.487C>T (p.Leu163=)
c.285C>T
n.873C>T
c.697C>T (p.Leu233=)
 gnomAD v4
4g.6291974T>ACA356172314WFS1c.689T>A (p.Leu230Gln)
c.666T>A
c.440T>A (p.Leu147Gln)
c.488T>A (p.Leu163Gln)
c.286T>A
n.874T>A
c.698T>A (p.Leu233Gln)
4g.6291974T>CCA356172315WFS1c.689T>C (p.Leu230Pro)
c.666T>C
c.440T>C (p.Leu147Pro)
c.488T>C (p.Leu163Pro)
c.286T>C
n.874T>C
c.698T>C (p.Leu233Pro)
 gnomAD v4
4g.6291974T>GCA356172316WFS1c.689T>G (p.Leu230Arg)
c.666T>G
c.440T>G (p.Leu147Arg)
c.488T>G (p.Leu163Arg)
c.286T>G
n.874T>G
c.698T>G (p.Leu233Arg)
4g.6291975G>ACA438211077WFS1c.690G>A (p.Leu230=)
c.667G>A
c.441G>A (p.Leu147=)
c.489G>A (p.Leu163=)
c.287G>A
n.875G>A
c.699G>A (p.Leu233=)
4g.6291975G>CCA438211078WFS1c.690G>C (p.Leu230=)
c.667G>C
c.441G>C (p.Leu147=)
c.489G>C (p.Leu163=)
c.287G>C
n.875G>C
c.699G>C (p.Leu233=)
 dbSNP gnomAD v2 gnomAD v4
4g.6291975G=CA1435768977WFS1c.690G= (p.Leu230=)
c.667G=
c.441G= (p.Leu147=)
c.489G= (p.Leu163=)
c.287G=
n.875G=
c.699G= (p.Leu233=)
4g.6291975G>TCA438211079WFS1c.690G>T (p.Leu230=)
c.667G>T
c.441G>T (p.Leu147=)
c.489G>T (p.Leu163=)
c.287G>T
n.875G>T
c.699G>T (p.Leu233=)
 gnomAD v4
4g.6291976G>ACA2838994WFS1c.691G>A (p.Glu231Lys)
c.668G>A
c.442G>A (p.Glu148Lys)
c.490G>A (p.Glu164Lys)
c.288G>A
n.876G>A
c.700G>A (p.Glu234Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6291976G>CCA356172317WFS1c.691G>C (p.Glu231Gln)
c.668G>C
c.442G>C (p.Glu148Gln)
c.490G>C (p.Glu164Gln)
c.288G>C
n.876G>C
c.700G>C (p.Glu234Gln)
4g.6291976G=CA1435768978WFS1c.691G= (p.Glu231=)
c.668G=
c.442G= (p.Glu148=)
c.490G= (p.Glu164=)
c.288G=
n.876G=
c.700G= (p.Glu234=)
4g.6291976G>TCA356172318WFS1c.691G>T (p.Glu231Ter)
c.668G>T
c.442G>T (p.Glu148Ter)
c.490G>T (p.Glu164Ter)
c.288G>T
n.876G>T
c.700G>T (p.Glu234Ter)
4g.6291977A=CA1435768979WFS1c.692A= (p.Glu231=)
c.669A=
c.443A= (p.Glu148=)
c.491A= (p.Glu164=)
c.289A=
n.877A=
c.701A= (p.Glu234=)
4g.6291977A>CCA356172319WFS1c.692A>C (p.Glu231Ala)
c.669A>C
c.443A>C (p.Glu148Ala)
c.491A>C (p.Glu164Ala)
c.289A>C
n.877A>C
c.701A>C (p.Glu234Ala)
4g.6291977A>GCA2838995WFS1c.692A>G (p.Glu231Gly)
c.669A>G
c.443A>G (p.Glu148Gly)
c.491A>G (p.Glu164Gly)
c.289A>G
n.877A>G
c.701A>G (p.Glu234Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6291977A>TCA356172320WFS1c.692A>T (p.Glu231Val)
c.669A>T
c.443A>T (p.Glu148Val)
c.491A>T (p.Glu164Val)
c.289A>T
n.877A>T
c.701A>T (p.Glu234Val)

Number of alleles fetched