Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107710035T>CCA2684468547SLC26A4c.2090-19T>C (n.2090-19T>C)
c.746-19T>C
n.377-120T>C
c.2012-19T>C (n.2012-19T>C)
 gnomAD v4
7g.107710036T>ACA4433044SLC26A4c.2090-18T>A (n.2090-18T>A)
c.746-18T>A
n.377-119T>A
c.2012-18T>A (n.2012-18T>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710036T=CA1732751137SLC26A4c.2090-18T= (n.2090-18T=)
c.746-18T=
n.377-119T=
c.2012-18T= (n.2012-18T=)
7g.107710037G>ACA4433045SLC26A4c.2090-17G>A (n.2090-17G>A)
c.746-17G>A
n.377-118G>A
c.2012-17G>A (n.2012-17G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710037G>CCA577030682SLC26A4c.2090-17G>C (n.2090-17G>C)
c.746-17G>C
n.377-118G>C
c.2012-17G>C (n.2012-17G>C)
 dbSNP gnomAD v2 gnomAD v4
7g.107710037G=CA1732751139SLC26A4c.2090-17G= (n.2090-17G=)
c.746-17G=
n.377-118G=
c.2012-17G= (n.2012-17G=)
7g.107710039G>ACA1732751143SLC26A4c.2090-15G>A (n.2090-15G>A)
c.746-15G>A
n.377-116G>A
c.2012-15G>A (n.2012-15G>A)
 ClinVar dbSNP gnomAD v4
7g.107710039G=CA1732751142SLC26A4c.2090-15G= (n.2090-15G=)
c.746-15G=
n.377-116G=
c.2012-15G= (n.2012-15G=)
7g.107710041C=CA1732751145SLC26A4c.2090-13C= (n.2090-13C=)
c.746-13C=
n.377-114C=
c.2012-13C= (n.2012-13C=)
7g.107710041C>TCA164227991SLC26A4c.2090-13C>T (n.2090-13C>T)
c.746-13C>T
n.377-114C>T
c.2012-13C>T (n.2012-13C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107710043T>CCA2697557505SLC26A4c.2090-11T>C (n.2090-11T>C)
c.746-11T>C
n.377-112T>C
c.2012-11T>C (n.2012-11T>C)
 ClinVar
7g.107710045C=CA1732751146SLC26A4c.2090-9C= (n.2090-9C=)
c.746-9C=
n.377-110C=
c.2012-9C= (n.2012-9C=)
7g.107710045C>GCA1732751147SLC26A4c.2090-9C>G (n.2090-9C>G)
c.746-9C>G
n.377-110C>G
c.2012-9C>G (n.2012-9C>G)
 dbSNP
7g.107710045C>TCA2684468548SLC26A4c.2090-9C>T (n.2090-9C>T)
c.746-9C>T
n.377-110C>T
c.2012-9C>T (n.2012-9C>T)
 gnomAD v4
7g.107710046T>CCA831174260SLC26A4c.2090-8T>C (n.2090-8T>C)
c.746-8T>C
n.377-109T>C
c.2012-8T>C (n.2012-8T>C)
 dbSNP gnomAD v3 gnomAD v4
7g.107710046T=CA1732751149SLC26A4c.2090-8T= (n.2090-8T=)
c.746-8T=
n.377-109T=
c.2012-8T= (n.2012-8T=)
7g.107710047T>CCA4433046SLC26A4c.2090-7T>C (n.2090-7T>C)
c.746-7T>C
n.377-108T>C
c.2012-7T>C (n.2012-7T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710047T=CA1732751150SLC26A4c.2090-7T= (n.2090-7T=)
c.746-7T=
n.377-108T=
c.2012-7T= (n.2012-7T=)
7g.107710049T>CCA2684468549SLC26A4c.2090-5T>C (n.2090-5T>C)
c.746-5T>C
n.377-106T>C
c.2012-5T>C (n.2012-5T>C)
 gnomAD v4
7g.107710049T>GCA577030683SLC26A4c.2090-5T>G (n.2090-5T>G)
c.746-5T>G
n.377-106T>G
c.2012-5T>G (n.2012-5T>G)
 dbSNP gnomAD v2 gnomAD v4
7g.107710049T=CA1732751152SLC26A4c.2090-5T= (n.2090-5T=)
c.746-5T=
n.377-106T=
c.2012-5T= (n.2012-5T=)
7g.107710050G>ACA2697557506SLC26A4c.2090-4G>A (n.2090-4G>A)
c.746-4G>A
n.377-105G>A
c.2012-4G>A (n.2012-4G>A)
 ClinVar
7g.107710050G>TCA2697557507SLC26A4c.2090-4G>T (n.2090-4G>T)
c.746-4G>T
n.377-105G>T
c.2012-4G>T (n.2012-4G>T)
 ClinVar
7g.107710052A>CCA368845398SLC26A4c.2090-2A>C (n.2090-2A>C)
c.746-2A>C
n.377-103A>C
c.2012-2A>C (n.2012-2A>C)
7g.107710052A>GCA368845403SLC26A4c.2090-2A>G (n.2090-2A>G)
c.746-2A>G
n.377-103A>G
c.2012-2A>G (n.2012-2A>G)
7g.107710052A>TCA368845400SLC26A4c.2090-2A>T (n.2090-2A>T)
c.746-2A>T
n.377-103A>T
c.2012-2A>T (n.2012-2A>T)
7g.107710053G>ACA368845406SLC26A4c.2090-1G>A (n.2090-1G>A)
c.746-1G>A
n.377-102G>A
c.2012-1G>A (n.2012-1G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710053G>CCA368845407SLC26A4c.2090-1G>C (n.2090-1G>C)
c.746-1G>C
n.377-102G>C
c.2012-1G>C (n.2012-1G>C)
7g.107710053G=CA1732751159SLC26A4c.2090-1G= (n.2090-1G=)
c.746-1G=
n.377-102G=
c.2012-1G= (n.2012-1G=)
7g.107710053G>TCA368845409SLC26A4c.2090-1G>T (n.2090-1G>T)
c.746-1G>T
n.377-102G>T
c.2012-1G>T (n.2012-1G>T)
7g.107710054A=CA1732751165SLC26A4c.2090A= (p.Asp697=)
c.746A=
n.377-101A=
c.2012A= (p.Asp671=)
7g.107710054A>CCA132697SLC26A4c.2090A>C (p.Asp697Ala)
c.746A>C
n.377-101A>C
c.2012A>C (p.Asp671Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710054A>GCA368845412SLC26A4c.2090A>G (p.Asp697Gly)
c.746A>G
n.377-101A>G
c.2012A>G (p.Asp671Gly)
 ClinVar gnomAD v4
7g.107710054A>TCA368845414SLC26A4c.2090A>T (p.Asp697Val)
c.746A>T
n.377-101A>T
c.2012A>T (p.Asp671Val)
7g.107710055T>ACA368845416SLC26A4c.2091T>A (p.Asp697Glu)
c.747T>A
n.377-100T>A
c.2013T>A (p.Asp671Glu)
7g.107710055T>CCA457104549SLC26A4c.2091T>C (p.Asp697=)
c.747T>C
n.377-100T>C
c.2013T>C (p.Asp671=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710055T>GCA368845418SLC26A4c.2091T>G (p.Asp697Glu)
c.747T>G
n.377-100T>G
c.2013T>G (p.Asp671Glu)
 ClinVar
7g.107710055T=CA1732751170SLC26A4c.2091T= (p.Asp697=)
c.747T=
n.377-100T=
c.2013T= (p.Asp671=)
7g.107710056T>ACA368845420SLC26A4c.2092T>A (p.Tyr698Asn)
c.748T>A
n.377-99T>A
c.2014T>A (p.Tyr672Asn)
7g.107710056T>CCA368845422SLC26A4c.2092T>C (p.Tyr698His)
c.748T>C
n.377-99T>C
c.2014T>C (p.Tyr672His)
7g.107710056T>GCA368845424SLC26A4c.2092T>G (p.Tyr698Asp)
c.748T>G
n.377-99T>G
c.2014T>G (p.Tyr672Asp)
7g.107710057A>CCA368845428SLC26A4c.2093A>C (p.Tyr698Ser)
c.749A>C
n.377-98A>C
c.2015A>C (p.Tyr672Ser)
7g.107710057A>GCA368845430SLC26A4c.2093A>G (p.Tyr698Cys)
c.749A>G
n.377-98A>G
c.2015A>G (p.Tyr672Cys)
 COSMIC
7g.107710057A>TCA368845426SLC26A4c.2093A>T (p.Tyr698Phe)
c.749A>T
n.377-98A>T
c.2015A>T (p.Tyr672Phe)
7g.107710058T>ACA368845434SLC26A4c.2094T>A (p.Tyr698Ter)
c.750T>A
n.377-97T>A
c.2016T>A (p.Tyr672Ter)
7g.107710058T>CCA457104552SLC26A4c.2094T>C (p.Tyr698=)
c.750T>C
n.377-97T>C
c.2016T>C (p.Tyr672=)
 ClinVar dbSNP
7g.107710058T>GCA368845432SLC26A4c.2094T>G (p.Tyr698Ter)
c.750T>G
n.377-97T>G
c.2016T>G (p.Tyr672Ter)
 gnomAD v4
7g.107710059G>ACA4433047SLC26A4c.2095G>A (p.Val699Met)
c.751G>A
n.377-96G>A
c.2017G>A (p.Val673Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710059G>CCA368845444SLC26A4c.2095G>C (p.Val699Leu)
c.751G>C
n.377-96G>C
c.2017G>C (p.Val673Leu)
7g.107710059G=CA1732751173SLC26A4c.2095G= (p.Val699=)
c.751G=
n.377-96G=
c.2017G= (p.Val673=)
7g.107710059G>TCA368845446SLC26A4c.2095G>T (p.Val699Leu)
c.751G>T
n.377-96G>T
c.2017G>T (p.Val673Leu)
7g.107710060T>ACA368845448SLC26A4c.2096T>A (p.Val699Glu)
c.752T>A
n.377-95T>A
c.2018T>A (p.Val673Glu)
7g.107710060T>CCA368845450SLC26A4c.2096T>C (p.Val699Ala)
c.752T>C
n.377-95T>C
c.2018T>C (p.Val673Ala)
 gnomAD v4
7g.107710060T>GCA368845451SLC26A4c.2096T>G (p.Val699Gly)
c.752T>G
n.377-95T>G
c.2018T>G (p.Val673Gly)
7g.107710061G>ACA164228021SLC26A4c.2097G>A (p.Val699=)
c.753G>A
n.377-94G>A
c.2019G>A (p.Val673=)
 dbSNP
7g.107710061G>CCA457104554SLC26A4c.2097G>C (p.Val699=)
c.753G>C
n.377-94G>C
c.2019G>C (p.Val673=)
7g.107710061G=CA1732751177SLC26A4c.2097G= (p.Val699=)
c.753G=
n.377-94G=
c.2019G= (p.Val673=)
7g.107710061G>TCA457104555SLC26A4c.2097G>T (p.Val699=)
c.753G>T
n.377-94G>T
c.2019G>T (p.Val673=)
7g.107710062A>CCA368845453SLC26A4c.2098A>C (p.Ile700Leu)
c.754A>C
n.377-93A>C
c.2020A>C (p.Ile674Leu)
7g.107710062A>GCA368845457SLC26A4c.2098A>G (p.Ile700Val)
c.754A>G
n.377-93A>G
c.2020A>G (p.Ile674Val)
 ClinVar gnomAD v4
7g.107710062A>TCA368845455SLC26A4c.2098A>T (p.Ile700Leu)
c.754A>T
n.377-93A>T
c.2020A>T (p.Ile674Leu)
7g.107710063T>ACA368845459SLC26A4c.2099T>A (p.Ile700Lys)
c.755T>A
n.377-92T>A
c.2021T>A (p.Ile674Lys)
7g.107710063T>CCA4433048SLC26A4c.2099T>C (p.Ile700Thr)
c.755T>C
n.377-92T>C
c.2021T>C (p.Ile674Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710063T>GCA368845462SLC26A4c.2099T>G (p.Ile700Arg)
c.755T>G
n.377-92T>G
c.2021T>G (p.Ile674Arg)
7g.107710063T=CA1732751179SLC26A4c.2099T= (p.Ile700=)
c.755T=
n.377-92T=
c.2021T= (p.Ile674=)
7g.107710064A=CA1732751183SLC26A4c.2100A= (p.Ile700=)
c.756A=
n.377-91A=
c.2022A= (p.Ile674=)
7g.107710064A>CCA457104559SLC26A4c.2100A>C (p.Ile700=)
c.756A>C
n.377-91A>C
c.2022A>C (p.Ile674=)
7g.107710064A>GCA16605617SLC26A4c.2100A>G (p.Ile700Met)
c.756A>G
n.377-91A>G
c.2022A>G (p.Ile674Met)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.107710064A>TCA457104560SLC26A4c.2100A>T (p.Ile700=)
c.756A>T
n.377-91A>T
c.2022A>T (p.Ile674=)
7g.107710065G>ACA368845463SLC26A4c.2101G>A (p.Glu701Lys)
c.757G>A
n.377-90G>A
c.2023G>A (p.Glu675Lys)
7g.107710065G>CCA368845467SLC26A4c.2101G>C (p.Glu701Gln)
c.757G>C
n.377-90G>C
c.2023G>C (p.Glu675Gln)
7g.107710065G>TCA368845465SLC26A4c.2101G>T (p.Glu701Ter)
c.757G>T
n.377-90G>T
c.2023G>T (p.Glu675Ter)
7g.107710066A>CCA368845468SLC26A4c.2102A>C (p.Glu701Ala)
c.758A>C
n.377-89A>C
c.2024A>C (p.Glu675Ala)
7g.107710066A>GCA368845471SLC26A4c.2102A>G (p.Glu701Gly)
c.758A>G
n.377-89A>G
c.2024A>G (p.Glu675Gly)
7g.107710066A>TCA368845472SLC26A4c.2102A>T (p.Glu701Val)
c.758A>T
n.377-89A>T
c.2024A>T (p.Glu675Val)
7g.107710067A>CCA368845474SLC26A4c.2103A>C (p.Glu701Asp)
c.759A>C
n.377-88A>C
c.2025A>C (p.Glu675Asp)
7g.107710067A>GCA457104562SLC26A4c.2103A>G (p.Glu701=)
c.759A>G
n.377-88A>G
c.2025A>G (p.Glu675=)
 gnomAD v4
7g.107710067A>TCA368845476SLC26A4c.2103A>T (p.Glu701Asp)
c.759A>T
n.377-88A>T
c.2025A>T (p.Glu675Asp)
7g.107710068A>CCA368845478SLC26A4c.2104A>C (p.Lys702Gln)
c.760A>C
n.377-87A>C
c.2026A>C (p.Lys676Gln)
7g.107710068A>GCA368845480SLC26A4c.2104A>G (p.Lys702Glu)
c.760A>G
n.377-87A>G
c.2026A>G (p.Lys676Glu)
7g.107710068A>TCA368845483SLC26A4c.2104A>T (p.Lys702Ter)
c.760A>T
n.377-87A>T
c.2026A>T (p.Lys676Ter)
7g.107710069A=CA1732751188SLC26A4c.2105A= (p.Lys702=)
c.761A=
n.377-86A=
c.2027A= (p.Lys676=)
7g.107710069A>CCA368845485SLC26A4c.2105A>C (p.Lys702Thr)
c.761A>C
n.377-86A>C
c.2027A>C (p.Lys676Thr)
7g.107710069A>GCA368845487SLC26A4c.2105A>G (p.Lys702Arg)
c.761A>G
n.377-86A>G
c.2027A>G (p.Lys676Arg)
7g.107710069A>TCA368845489SLC26A4c.2105A>T (p.Lys702Met)
c.761A>T
n.377-86A>T
c.2027A>T (p.Lys676Met)
7g.107710069_107710070delinsAGCA1732751187SLC26A4c.2105_2106delinsAG (p.Lys702=)
c.761_762delinsAG
n.377-86_377-85delinsAG
c.2027_2028delinsAG (p.Lys676=)
7g.107710070delCA577030684SLC26A4c.2106del (p.Lys702AsnfsTer19)
c.762del
n.377-85del
c.2028del (p.Lys676AsnfsTer19)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710070G>ACA457104563SLC26A4c.2106G>A (p.Lys702=)
c.762G>A
n.377-85G>A
c.2028G>A (p.Lys676=)
7g.107710070G>CCA4433049SLC26A4c.2106G>C (p.Lys702Asn)
c.762G>C
n.377-85G>C
c.2028G>C (p.Lys676Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710070G=CA1732751197SLC26A4c.2106G= (p.Lys702=)
c.762G=
n.377-85G=
c.2028G= (p.Lys676=)
7g.107710070G>TCA368845492SLC26A4c.2106G>T (p.Lys702Asn)
c.762G>T
n.377-85G>T
c.2028G>T (p.Lys676Asn)
7g.107710070_107710074dupCA658656001SLC26A4c.2106_2110dup (p.Glu704GlyfsTer19)
c.762_766dup
n.377-85_377-81dup
c.2028_2032dup (p.Glu678GlyfsTer19)
 ClinVar dbSNP
7g.107710071C>ACA368845494SLC26A4c.2107C>A (p.Leu703Met)
c.763C>A
n.377-84C>A
c.2029C>A (p.Leu677Met)
7g.107710071C>GCA368845496SLC26A4c.2107C>G (p.Leu703Val)
c.763C>G
n.377-84C>G
c.2029C>G (p.Leu677Val)
 ClinVar dbSNP
7g.107710071C>TCA457104564SLC26A4c.2107C>T (p.Leu703=)
c.763C>T
n.377-84C>T
c.2029C>T (p.Leu677=)
7g.107710072T>ACA368845499SLC26A4c.2108T>A (p.Leu703Gln)
c.764T>A
n.377-83T>A
c.2030T>A (p.Leu677Gln)
7g.107710072T>CCA368845501SLC26A4c.2108T>C (p.Leu703Pro)
c.764T>C
n.377-83T>C
c.2030T>C (p.Leu677Pro)
 ClinVar dbSNP gnomAD v4
7g.107710072T>GCA368845503SLC26A4c.2108T>G (p.Leu703Arg)
c.764T>G
n.377-83T>G
c.2030T>G (p.Leu677Arg)
7g.107710072T=CA1732751202SLC26A4c.2108T= (p.Leu703=)
c.764T=
n.377-83T=
c.2030T= (p.Leu677=)
7g.107710073G>ACA457104567SLC26A4c.2109G>A (p.Leu703=)
c.765G>A
n.377-82G>A
c.2031G>A (p.Leu677=)
 gnomAD v4
7g.107710073G>CCA457104568SLC26A4c.2109G>C (p.Leu703=)
c.765G>C
n.377-82G>C
c.2031G>C (p.Leu677=)
7g.107710073G>TCA457104569SLC26A4c.2109G>T (p.Leu703=)
c.765G>T
n.377-82G>T
c.2031G>T (p.Leu677=)
7g.107710073_107710074delCA2580076182SLC26A4c.2109_2110del (p.Glu704AlafsTer6)
c.765_766del
n.377-82_377-81del
c.2031_2032del (p.Glu678AlafsTer6)
 ClinVar
7g.107710074G>ACA368845507SLC26A4c.2110G>A (p.Glu704Lys)
c.766G>A
n.377-81G>A
c.2032G>A (p.Glu678Lys)
 ClinVar dbSNP gnomAD v4
7g.107710074G>CCA4433050SLC26A4c.2110G>C (p.Glu704Gln)
c.766G>C
n.377-81G>C
c.2032G>C (p.Glu678Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710074G=CA1732751206SLC26A4c.2110G= (p.Glu704=)
c.766G=
n.377-81G=
c.2032G= (p.Glu678=)
7g.107710074G>TCA368845511SLC26A4c.2110G>T (p.Glu704Ter)
c.766G>T
n.377-81G>T
c.2032G>T (p.Glu678Ter)
7g.107710075A>CCA368845515SLC26A4c.2111A>C (p.Glu704Ala)
c.767A>C
n.377-80A>C
c.2033A>C (p.Glu678Ala)
7g.107710075A>GCA368845518SLC26A4c.2111A>G (p.Glu704Gly)
c.767A>G
n.377-80A>G
c.2033A>G (p.Glu678Gly)
7g.107710075A>TCA368845520SLC26A4c.2111A>T (p.Glu704Val)
c.767A>T
n.377-80A>T
c.2033A>T (p.Glu678Val)
7g.107710076G>ACA457104571SLC26A4c.2112G>A (p.Glu704=)
c.768G>A
n.377-79G>A
c.2034G>A (p.Glu678=)
 gnomAD v4
7g.107710076G>CCA368845524SLC26A4c.2112G>C (p.Glu704Asp)
c.768G>C
n.377-79G>C
c.2034G>C (p.Glu678Asp)
7g.107710076G>TCA368845526SLC26A4c.2112G>T (p.Glu704Asp)
c.768G>T
n.377-79G>T
c.2034G>T (p.Glu678Asp)
7g.107710077C>ACA368845531SLC26A4c.2113C>A (p.Gln705Lys)
c.769C>A
n.377-78C>A
c.2035C>A (p.Gln679Lys)
7g.107710077C>GCA368845532SLC26A4c.2113C>G (p.Gln705Glu)
c.769C>G
n.377-78C>G
c.2035C>G (p.Gln679Glu)
7g.107710077C>TCA368845528SLC26A4c.2113C>T (p.Gln705Ter)
c.769C>T
n.377-78C>T
c.2035C>T (p.Gln679Ter)
 ClinVar
7g.107710078A>CCA368845533SLC26A4c.2114A>C (p.Gln705Pro)
c.770A>C
n.377-77A>C
c.2036A>C (p.Gln679Pro)
7g.107710078A>GCA368845534SLC26A4c.2114A>G (p.Gln705Arg)
c.770A>G
n.377-77A>G
c.2036A>G (p.Gln679Arg)
7g.107710078A>TCA368845535SLC26A4c.2114A>T (p.Gln705Leu)
c.770A>T
n.377-77A>T
c.2036A>T (p.Gln679Leu)
7g.107710079A=CA1732751210SLC26A4c.2115A= (p.Gln705=)
c.771A=
n.377-76A=
c.2037A= (p.Gln679=)
7g.107710079A>CCA368845537SLC26A4c.2115A>C (p.Gln705His)
c.771A>C
n.377-76A>C
c.2037A>C (p.Gln679His)
7g.107710079A>GCA457104573SLC26A4c.2115A>G (p.Gln705=)
c.771A>G
n.377-76A>G
c.2037A>G (p.Gln679=)
 ClinVar
7g.107710079A>TCA368845539SLC26A4c.2115A>T (p.Gln705His)
c.771A>T
n.377-76A>T
c.2037A>T (p.Gln679His)
 dbSNP gnomAD v4
7g.107710080T>ACA368845546SLC26A4c.2116T>A (p.Cys706Ser)
c.772T>A
n.377-75T>A
c.2038T>A (p.Cys680Ser)
7g.107710080T>CCA368845544SLC26A4c.2116T>C (p.Cys706Arg)
c.772T>C
n.377-75T>C
c.2038T>C (p.Cys680Arg)
 gnomAD v4
7g.107710080T>GCA368845541SLC26A4c.2116T>G (p.Cys706Gly)
c.772T>G
n.377-75T>G
c.2038T>G (p.Cys680Gly)
7g.107710081G>ACA368845550SLC26A4c.2117G>A (p.Cys706Tyr)
c.773G>A
n.377-74G>A
c.2039G>A (p.Cys680Tyr)
7g.107710081G>CCA368845553SLC26A4c.2117G>C (p.Cys706Ser)
c.773G>C
n.377-74G>C
c.2039G>C (p.Cys680Ser)
7g.107710081G>TCA368845556SLC26A4c.2117G>T (p.Cys706Phe)
c.773G>T
n.377-74G>T
c.2039G>T (p.Cys680Phe)
7g.107710082C>ACA4433051SLC26A4c.2118C>A (p.Cys706Ter)
c.774C>A
n.377-73C>A
c.2040C>A (p.Cys680Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710082C=CA1732751215SLC26A4c.2118C= (p.Cys706=)
c.774C=
n.377-73C=
c.2040C= (p.Cys680=)
7g.107710082C>GCA368845561SLC26A4c.2118C>G (p.Cys706Trp)
c.774C>G
n.377-73C>G
c.2040C>G (p.Cys680Trp)
7g.107710082C>TCA4433052SLC26A4c.2118C>T (p.Cys706=)
c.774C>T
n.377-73C>T
c.2040C>T (p.Cys680=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710083G>ACA164228038SLC26A4c.2119G>A (p.Gly707Arg)
c.775G>A
n.377-72G>A
c.2041G>A (p.Gly681Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.107710083G>CCA368845570SLC26A4c.2119G>C (p.Gly707Arg)
c.775G>C
n.377-72G>C
c.2041G>C (p.Gly681Arg)
 dbSNP gnomAD v2 gnomAD v4
7g.107710083G=CA1732751223SLC26A4c.2119G= (p.Gly707=)
c.775G=
n.377-72G=
c.2041G= (p.Gly681=)
7g.107710083G>TCA368845567SLC26A4c.2119G>T (p.Gly707Trp)
c.775G>T
n.377-72G>T
c.2041G>T (p.Gly681Trp)
 gnomAD v4
7g.107710084G>ACA368845574SLC26A4c.2120G>A (p.Gly707Glu)
c.776G>A
n.377-71G>A
c.2042G>A (p.Gly681Glu)
 gnomAD v4 COSMIC
7g.107710084G>CCA368845578SLC26A4c.2120G>C (p.Gly707Ala)
c.776G>C
n.377-71G>C
c.2042G>C (p.Gly681Ala)
7g.107710084G>TCA368845576SLC26A4c.2120G>T (p.Gly707Val)
c.776G>T
n.377-71G>T
c.2042G>T (p.Gly681Val)
 ClinVar dbSNP gnomAD v4
7g.107710085G>ACA457104578SLC26A4c.2121G>A (p.Gly707=)
c.777G>A
n.377-70G>A
c.2043G>A (p.Gly681=)
7g.107710085G>CCA457104579SLC26A4c.2121G>C (p.Gly707=)
c.777G>C
n.377-70G>C
c.2043G>C (p.Gly681=)
7g.107710085G=CA1732751226SLC26A4c.2121G= (p.Gly707=)
c.777G=
n.377-70G=
c.2043G= (p.Gly681=)
7g.107710085G>TCA457104577SLC26A4c.2121G>T (p.Gly707=)
c.777G>T
n.377-70G>T
c.2043G>T (p.Gly681=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107710086T>ACA368845580SLC26A4c.2122T>A (p.Phe708Ile)
c.778T>A
n.377-69T>A
c.2044T>A (p.Phe682Ile)
7g.107710086T>CCA368845586SLC26A4c.2122T>C (p.Phe708Leu)
c.778T>C
n.377-69T>C
c.2044T>C (p.Phe682Leu)
 gnomAD v4
7g.107710086T>GCA368845583SLC26A4c.2122T>G (p.Phe708Val)
c.778T>G
n.377-69T>G
c.2044T>G (p.Phe682Val)
7g.107710087T>ACA368845589SLC26A4c.2123T>A (p.Phe708Tyr)
c.779T>A
n.377-68T>A
c.2045T>A (p.Phe682Tyr)
7g.107710087T>CCA368845594SLC26A4c.2123T>C (p.Phe708Ser)
c.779T>C
n.377-68T>C
c.2045T>C (p.Phe682Ser)
7g.107710087T>GCA368845592SLC26A4c.2123T>G (p.Phe708Cys)
c.779T>G
n.377-68T>G
c.2045T>G (p.Phe682Cys)
7g.107710088delCA2695208259SLC26A4c.2124del (p.Phe709LeufsTer12)
c.780del
n.377-67del
c.2046del (p.Phe683LeufsTer12)
7g.107710088C>ACA368845597SLC26A4c.2124C>A (p.Phe708Leu)
c.780C>A
n.377-67C>A
c.2046C>A (p.Phe682Leu)
 gnomAD v4 COSMIC
7g.107710088C=CA1732751233SLC26A4c.2124C= (p.Phe708=)
c.780C=
n.377-67C=
c.2046C= (p.Phe682=)
7g.107710088C>GCA368845601SLC26A4c.2124C>G (p.Phe708Leu)
c.780C>G
n.377-67C>G
c.2046C>G (p.Phe682Leu)
7g.107710088C>TCA457104580SLC26A4c.2124C>T (p.Phe708=)
c.780C>T
n.377-67C>T
c.2046C>T (p.Phe682=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710088_107710089delinsCTCA1732751230SLC26A4c.2124_2125delinsCT (p.Phe708=)
c.780_781delinsCT
n.377-67_377-66delinsCT
c.2046_2047delinsCT (p.Phe682=)
7g.107710089T>ACA368845607SLC26A4c.2125T>A (p.Phe709Ile)
c.781T>A
n.377-66T>A
c.2047T>A (p.Phe683Ile)
7g.107710089T>CCA368845622SLC26A4c.2125T>C (p.Phe709Leu)
c.781T>C
n.377-66T>C
c.2047T>C (p.Phe683Leu)
7g.107710089T>GCA368845618SLC26A4c.2125T>G (p.Phe709Val)
c.781T>G
n.377-66T>G
c.2047T>G (p.Phe683Val)
7g.107710091delCA274062SLC26A4c.2127del (p.Phe709LeufsTer12)
c.783del
n.377-64del
c.2049del (p.Phe683LeufsTer12)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710090T>ACA368845626SLC26A4c.2126T>A (p.Phe709Tyr)
c.782T>A
n.377-65T>A
c.2048T>A (p.Phe683Tyr)
7g.107710090T>CCA368845629SLC26A4c.2126T>C (p.Phe709Ser)
c.782T>C
n.377-65T>C
c.2048T>C (p.Phe683Ser)
7g.107710090T>GCA368845631SLC26A4c.2126T>G (p.Phe709Cys)
c.782T>G
n.377-65T>G
c.2048T>G (p.Phe683Cys)
7g.107710091T>ACA368845635SLC26A4c.2127T>A (p.Phe709Leu)
c.783T>A
n.377-64T>A
c.2049T>A (p.Phe683Leu)
7g.107710091T>CCA457104582SLC26A4c.2127T>C (p.Phe709=)
c.783T>C
n.377-64T>C
c.2049T>C (p.Phe683=)
7g.107710091T>GCA368845636SLC26A4c.2127T>G (p.Phe709Leu)
c.783T>G
n.377-64T>G
c.2049T>G (p.Phe683Leu)
7g.107710092G>ACA368845640SLC26A4c.2128G>A (p.Asp710Asn)
c.784G>A
n.377-63G>A
c.2050G>A (p.Asp684Asn)
 gnomAD v4
7g.107710092G>CCA368845641SLC26A4c.2128G>C (p.Asp710His)
c.784G>C
n.377-63G>C
c.2050G>C (p.Asp684His)
 gnomAD v4
7g.107710092G=CA1732751241SLC26A4c.2128G= (p.Asp710=)
c.784G=
n.377-63G=
c.2050G= (p.Asp684=)
7g.107710092G>TCA368845642SLC26A4c.2128G>T (p.Asp710Tyr)
c.784G>T
n.377-63G>T
c.2050G>T (p.Asp684Tyr)
 dbSNP
7g.107710093A>CCA368845643SLC26A4c.2129A>C (p.Asp710Ala)
c.785A>C
n.377-62A>C
c.2051A>C (p.Asp684Ala)
7g.107710093A>GCA368845644SLC26A4c.2129A>G (p.Asp710Gly)
c.785A>G
n.377-62A>G
c.2051A>G (p.Asp684Gly)
7g.107710093A>TCA368845645SLC26A4c.2129A>T (p.Asp710Val)
c.785A>T
n.377-62A>T
c.2051A>T (p.Asp684Val)
7g.107710094C>ACA368845650SLC26A4c.2130C>A (p.Asp710Glu)
c.786C>A
n.377-61C>A
c.2052C>A (p.Asp684Glu)
 dbSNP gnomAD v4
7g.107710094C=CA1732751246SLC26A4c.2130C= (p.Asp710=)
c.786C=
n.377-61C=
c.2052C= (p.Asp684=)
7g.107710094C>GCA368845649SLC26A4c.2130C>G (p.Asp710Glu)
c.786C>G
n.377-61C>G
c.2052C>G (p.Asp684Glu)
7g.107710094C>TCA132701SLC26A4c.2130C>T (p.Asp710=)
c.786C>T
n.377-61C>T
c.2052C>T (p.Asp684=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710095G>ACA132703SLC26A4c.2131G>A (p.Asp711Asn)
c.787G>A
n.377-60G>A
c.2053G>A (p.Asp685Asn)
 ClinVar dbSNP gnomAD v4 COSMIC
7g.107710095G>CCA368845655SLC26A4c.2131G>C (p.Asp711His)
c.787G>C
n.377-60G>C
c.2053G>C (p.Asp685His)
7g.107710095G=CA1732751254SLC26A4c.2131G= (p.Asp711=)
c.787G=
n.377-60G=
c.2053G= (p.Asp685=)
7g.107710095G>TCA4433053SLC26A4c.2131G>T (p.Asp711Tyr)
c.787G>T
n.377-60G>T
c.2053G>T (p.Asp685Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710095_107710098delCA913111823SLC26A4c.2131_2134del (p.Asp711ThrfsTer9)
c.787_790del
n.377-60_377-57del
c.2053_2056del (p.Asp685ThrfsTer9)
7g.107710095_107710098delinsGACACA1732751252SLC26A4c.2131_2134delinsGACA (p.Asp711=)
c.787_790delinsGACA
n.377-60_377-57delinsGACA
c.2053_2056delinsGACA (p.Asp685=)
7g.107710096A=CA1732751259SLC26A4c.2132A= (p.Asp711=)
c.788A=
n.377-59A=
c.2054A= (p.Asp685=)
7g.107710096A>CCA368845659SLC26A4c.2132A>C (p.Asp711Ala)
c.788A>C
n.377-59A>C
c.2054A>C (p.Asp685Ala)
7g.107710096A>GCA368845664SLC26A4c.2132A>G (p.Asp711Gly)
c.788A>G
n.377-59A>G
c.2054A>G (p.Asp685Gly)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107710096A>TCA368845667SLC26A4c.2132A>T (p.Asp711Val)
c.788A>T
n.377-59A>T
c.2054A>T (p.Asp685Val)
7g.107710099_107710101delCA658821811SLC26A4c.2135_2137del (p.Asn712del)
c.791_793del
n.377-56_377-54del
c.2057_2059del (p.Asn686del)
 ClinVar dbSNP
7g.107710097C>ACA368845668SLC26A4c.2133C>A (p.Asp711Glu)
c.789C>A
n.377-58C>A
c.2055C>A (p.Asp685Glu)
7g.107710097C>GCA368845670SLC26A4c.2133C>G (p.Asp711Glu)
c.789C>G
n.377-58C>G
c.2055C>G (p.Asp685Glu)
7g.107710097C>TCA457104587SLC26A4c.2133C>T (p.Asp711=)
c.789C>T
n.377-58C>T
c.2055C>T (p.Asp685=)
 gnomAD v4
7g.107710098A=CA1732751265SLC26A4c.2134A= (p.Asn712=)
c.790A=
n.377-57A=
c.2056A= (p.Asn686=)
7g.107710098A>CCA368845672SLC26A4c.2134A>C (p.Asn712His)
c.790A>C
n.377-57A>C
c.2056A>C (p.Asn686His)
7g.107710098A>GCA368845675SLC26A4c.2134A>G (p.Asn712Asp)
c.790A>G
n.377-57A>G
c.2056A>G (p.Asn686Asp)
 dbSNP
7g.107710098A>TCA368845679SLC26A4c.2134A>T (p.Asn712Tyr)
c.790A>T
n.377-57A>T
c.2056A>T (p.Asn686Tyr)
7g.107710099A=CA1732751269SLC26A4c.2135A= (p.Asn712=)
c.791A=
n.377-56A=
c.2057A= (p.Asn686=)
7g.107710099A>CCA368845684SLC26A4c.2135A>C (p.Asn712Thr)
c.791A>C
n.377-56A>C
c.2057A>C (p.Asn686Thr)
7g.107710099A>GCA4433054SLC26A4c.2135A>G (p.Asn712Ser)
c.791A>G
n.377-56A>G
c.2057A>G (p.Asn686Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710099A>TCA368845682SLC26A4c.2135A>T (p.Asn712Ile)
c.791A>T
n.377-56A>T
c.2057A>T (p.Asn686Ile)
7g.107710100C>ACA368845689SLC26A4c.2136C>A (p.Asn712Lys)
c.792C>A
n.377-55C>A
c.2058C>A (p.Asn686Lys)
7g.107710100C>GCA368845699SLC26A4c.2136C>G (p.Asn712Lys)
c.792C>G
n.377-55C>G
c.2058C>G (p.Asn686Lys)
7g.107710100C>TCA457104588SLC26A4c.2136C>T (p.Asn712=)
c.792C>T
n.377-55C>T
c.2058C>T (p.Asn686=)
 dbSNP
7g.107710101delCA2695208260SLC26A4c.2137del (p.Ile713LeufsTer8)
c.793del
n.377-54del
c.2059del (p.Ile687LeufsTer8)
7g.107710101A=CA1732751273SLC26A4c.2137A= (p.Ile713=)
c.793A=
n.377-54A=
c.2059A= (p.Ile687=)
7g.107710101A>CCA368845700SLC26A4c.2137A>C (p.Ile713Leu)
c.793A>C
n.377-54A>C
c.2059A>C (p.Ile687Leu)
7g.107710101A>GCA4433055SLC26A4c.2137A>G (p.Ile713Val)
c.793A>G
n.377-54A>G
c.2059A>G (p.Ile687Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710101A>TCA368845708SLC26A4c.2137A>T (p.Ile713Phe)
c.793A>T
n.377-54A>T
c.2059A>T (p.Ile687Phe)
7g.107710102T>ACA368845710SLC26A4c.2138T>A (p.Ile713Asn)
c.794T>A
n.377-53T>A
c.2060T>A (p.Ile687Asn)
7g.107710102T>CCA368845713SLC26A4c.2138T>C (p.Ile713Thr)
c.794T>C
n.377-53T>C
c.2060T>C (p.Ile687Thr)
7g.107710102T>GCA4433056SLC26A4c.2138T>G (p.Ile713Ser)
c.794T>G
n.377-53T>G
c.2060T>G (p.Ile687Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710102T=CA1732751279SLC26A4c.2138T= (p.Ile713=)
c.794T=
n.377-53T=
c.2060T= (p.Ile687=)
7g.107710103delCA2499218644SLC26A4c.2139del (p.Arg714GlufsTer7)
c.795del
n.377-52del
c.2061del (p.Arg688GlufsTer7)
 ClinVar dbSNP
7g.107710103T>ACA457104589SLC26A4c.2139T>A (p.Ile713=)
c.795T>A
n.377-52T>A
c.2061T>A (p.Ile687=)
 gnomAD v4
7g.107710103T>CCA457104590SLC26A4c.2139T>C (p.Ile713=)
c.795T>C
n.377-52T>C
c.2061T>C (p.Ile687=)
7g.107710103T>GCA132705SLC26A4c.2139T>G (p.Ile713Met)
c.795T>G
n.377-52T>G
c.2061T>G (p.Ile687Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710103T=CA1732751283SLC26A4c.2139T= (p.Ile713=)
c.795T=
n.377-52T=
c.2061T= (p.Ile687=)
7g.107710104A>CCA457104591SLC26A4c.2140A>C (p.Arg714=)
c.796A>C
n.377-51A>C
c.2062A>C (p.Arg688=)
7g.107710104A>GCA368845721SLC26A4c.2140A>G (p.Arg714Gly)
c.796A>G
n.377-51A>G
c.2062A>G (p.Arg688Gly)
7g.107710104A>TCA368845723SLC26A4c.2140A>T (p.Arg714Ter)
c.796A>T
n.377-51A>T
c.2062A>T (p.Arg688Ter)
7g.107710105G>ACA368845737SLC26A4c.2141G>A (p.Arg714Lys)
c.797G>A
n.377-50G>A
c.2063G>A (p.Arg688Lys)
7g.107710105G>CCA368845741SLC26A4c.2141G>C (p.Arg714Thr)
c.797G>C
n.377-50G>C
c.2063G>C (p.Arg688Thr)
7g.107710105G>TCA368845732SLC26A4c.2141G>T (p.Arg714Ile)
c.797G>T
n.377-50G>T
c.2063G>T (p.Arg688Ile)
7g.107710106A>CCA368845744SLC26A4c.2142A>C (p.Arg714Ser)
c.798A>C
n.377-49A>C
c.2064A>C (p.Arg688Ser)
7g.107710106A>GCA457104592SLC26A4c.2142A>G (p.Arg714=)
c.798A>G
n.377-49A>G
c.2064A>G (p.Arg688=)
7g.107710106A>TCA368845747SLC26A4c.2142A>T (p.Arg714Ser)
c.798A>T
n.377-49A>T
c.2064A>T (p.Arg688Ser)
7g.107710107A>CCA368845749SLC26A4c.2143A>C (p.Lys715Gln)
c.799A>C
n.377-48A>C
c.2065A>C (p.Lys689Gln)
7g.107710107A>GCA368845753SLC26A4c.2143A>G (p.Lys715Glu)
c.799A>G
n.377-48A>G
c.2065A>G (p.Lys689Glu)
7g.107710107A>TCA368845754SLC26A4c.2143A>T (p.Lys715Ter)
c.799A>T
n.377-48A>T
c.2065A>T (p.Lys689Ter)
7g.107710108A=CA1732751288SLC26A4c.2144A= (p.Lys715=)
c.800A=
n.377-47A=
c.2066A= (p.Lys689=)
7g.107710108A>CCA368845759SLC26A4c.2144A>C (p.Lys715Thr)
c.800A>C
n.377-47A>C
c.2066A>C (p.Lys689Thr)
7g.107710108A>GCA368845755SLC26A4c.2144A>G (p.Lys715Arg)
c.800A>G
n.377-47A>G
c.2066A>G (p.Lys689Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710108A>TCA368845757SLC26A4c.2144A>T (p.Lys715Met)
c.800A>T
n.377-47A>T
c.2066A>T (p.Lys689Met)
7g.107710109G>ACA457104593SLC26A4c.2145G>A (p.Lys715=)
c.801G>A
n.377-46G>A
c.2067G>A (p.Lys689=)
 gnomAD v4
7g.107710109G>CCA368845764SLC26A4c.2145G>C (p.Lys715Asn)
c.801G>C
n.377-46G>C
c.2067G>C (p.Lys689Asn)
7g.107710109G=CA1732751294SLC26A4c.2145G= (p.Lys715=)
c.801G=
n.377-46G=
c.2067G= (p.Lys689=)
7g.107710109G>TCA261425SLC26A4c.2145G>T (p.Lys715Asn)
c.801G>T
n.377-46G>T
c.2067G>T (p.Lys689Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710110G>ACA4433057SLC26A4c.2146G>A (p.Asp716Asn)
c.802G>A
n.377-45G>A
c.2068G>A (p.Asp690Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710110G>CCA368845765SLC26A4c.2146G>C (p.Asp716His)
c.802G>C
n.377-45G>C
c.2068G>C (p.Asp690His)
7g.107710110G=CA1732751298SLC26A4c.2146G= (p.Asp716=)
c.802G=
n.377-45G=
c.2068G= (p.Asp690=)
7g.107710110G>TCA368845766SLC26A4c.2146G>T (p.Asp716Tyr)
c.802G>T
n.377-45G>T
c.2068G>T (p.Asp690Tyr)
7g.107710111A=CA1732751301SLC26A4c.2147A= (p.Asp716=)
c.803A=
n.377-44A=
c.2069A= (p.Asp690=)
7g.107710111A>CCA368845773SLC26A4c.2147A>C (p.Asp716Ala)
c.803A>C
n.377-44A>C
c.2069A>C (p.Asp690Ala)
7g.107710111A>GCA368845772SLC26A4c.2147A>G (p.Asp716Gly)
c.803A>G
n.377-44A>G
c.2069A>G (p.Asp690Gly)
 dbSNP gnomAD v4
7g.107710111A>TCA368845769SLC26A4c.2147A>T (p.Asp716Val)
c.803A>T
n.377-44A>T
c.2069A>T (p.Asp690Val)
7g.107710112C>ACA368845775SLC26A4c.2148C>A (p.Asp716Glu)
c.804C>A
n.377-43C>A
c.2070C>A (p.Asp690Glu)
7g.107710112C>GCA368845777SLC26A4c.2148C>G (p.Asp716Glu)
c.804C>G
n.377-43C>G
c.2070C>G (p.Asp690Glu)
7g.107710112C>TCA457104594SLC26A4c.2148C>T (p.Asp716=)
c.804C>T
n.377-43C>T
c.2070C>T (p.Asp690=)
 ClinVar
7g.107710113A>CCA368845782SLC26A4c.2149A>C (p.Thr717Pro)
c.805A>C
n.377-42A>C
c.2071A>C (p.Thr691Pro)
7g.107710113A>GCA368845783SLC26A4c.2149A>G (p.Thr717Ala)
c.805A>G
n.377-42A>G
c.2071A>G (p.Thr691Ala)
7g.107710113A>TCA368845784SLC26A4c.2149A>T (p.Thr717Ser)
c.805A>T
n.377-42A>T
c.2071A>T (p.Thr691Ser)
7g.107710114C>ACA368845786SLC26A4c.2150C>A (p.Thr717Lys)
c.806C>A
n.377-41C>A
c.2072C>A (p.Thr691Lys)
 gnomAD v4
7g.107710114C=CA1732751303SLC26A4c.2150C= (p.Thr717=)
c.806C=
n.377-41C=
c.2072C= (p.Thr691=)
7g.107710114C>GCA4433058SLC26A4c.2150C>G (p.Thr717Arg)
c.806C>G
n.377-41C>G
c.2072C>G (p.Thr691Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710114C>TCA368845787SLC26A4c.2150C>T (p.Thr717Ile)
c.806C>T
n.377-41C>T
c.2072C>T (p.Thr691Ile)
 ClinVar gnomAD v4 COSMIC
7g.107710115A=CA1732751306SLC26A4c.2151A= (p.Thr717=)
c.807A=
n.377-40A=
c.2073A= (p.Thr691=)
7g.107710115A>CCA4433059SLC26A4c.2151A>C (p.Thr717=)
c.807A>C
n.377-40A>C
c.2073A>C (p.Thr691=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710115A>GCA457104595SLC26A4c.2151A>G (p.Thr717=)
c.807A>G
n.377-40A>G
c.2073A>G (p.Thr691=)
7g.107710115A>TCA457104596SLC26A4c.2151A>T (p.Thr717=)
c.807A>T
n.377-40A>T
c.2073A>T (p.Thr691=)
7g.107710116T>ACA368845789SLC26A4c.2152T>A (p.Phe718Ile)
c.808T>A
n.377-39T>A
c.2074T>A (p.Phe692Ile)
7g.107710116T>CCA368845792SLC26A4c.2152T>C (p.Phe718Leu)
c.808T>C
n.377-39T>C
c.2074T>C (p.Phe692Leu)
7g.107710116T>GCA368845796SLC26A4c.2152T>G (p.Phe718Val)
c.808T>G
n.377-39T>G
c.2074T>G (p.Phe692Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.107710116T=CA1732751309SLC26A4c.2152T= (p.Phe718=)
c.808T=
n.377-39T=
c.2074T= (p.Phe692=)
7g.107710117T>ACA368845798SLC26A4c.2153T>A (p.Phe718Tyr)
c.809T>A
n.377-38T>A
c.2075T>A (p.Phe692Tyr)
 dbSNP
7g.107710117T>CCA4433060SLC26A4c.2153T>C (p.Phe718Ser)
c.809T>C
n.377-38T>C
c.2075T>C (p.Phe692Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710117T>GCA368845800SLC26A4c.2153T>G (p.Phe718Cys)
c.809T>G
n.377-38T>G
c.2075T>G (p.Phe692Cys)
7g.107710117T=CA1732751315SLC26A4c.2153T= (p.Phe718=)
c.809T=
n.377-38T=
c.2075T= (p.Phe692=)
7g.107710118C>ACA368845801SLC26A4c.2154C>A (p.Phe718Leu)
c.810C>A
n.377-37C>A
c.2076C>A (p.Phe692Leu)
7g.107710118C=CA1732751318SLC26A4c.2154C= (p.Phe718=)
c.810C=
n.377-37C=
c.2076C= (p.Phe692=)
7g.107710118C>GCA164228083SLC26A4c.2154C>G (p.Phe718Leu)
c.810C>G
n.377-37C>G
c.2076C>G (p.Phe692Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107710118C>TCA457104597SLC26A4c.2154C>T (p.Phe718=)
c.810C>T
n.377-37C>T
c.2076C>T (p.Phe692=)
7g.107710119T>ACA368845802SLC26A4c.2155T>A (p.Phe719Ile)
c.811T>A
n.377-36T>A
c.2077T>A (p.Phe693Ile)
7g.107710119T>CCA368845804SLC26A4c.2155T>C (p.Phe719Leu)
c.811T>C
n.377-36T>C
c.2077T>C (p.Phe693Leu)
7g.107710119T>GCA368845805SLC26A4c.2155T>G (p.Phe719Val)
c.811T>G
n.377-36T>G
c.2077T>G (p.Phe693Val)
7g.107710120T>ACA368845807SLC26A4c.2156T>A (p.Phe719Tyr)
c.812T>A
n.377-35T>A
c.2078T>A (p.Phe693Tyr)
7g.107710120T>CCA368845809SLC26A4c.2156T>C (p.Phe719Ser)
c.812T>C
n.377-35T>C
c.2078T>C (p.Phe693Ser)
7g.107710120T>GCA368845811SLC26A4c.2156T>G (p.Phe719Cys)
c.812T>G
n.377-35T>G
c.2078T>G (p.Phe693Cys)
 COSMIC
7g.107710121T>ACA368845812SLC26A4c.2157T>A (p.Phe719Leu)
c.813T>A
n.377-34T>A
c.2079T>A (p.Phe693Leu)
7g.107710121T>CCA457104599SLC26A4c.2157T>C (p.Phe719=)
c.813T>C
n.377-34T>C
c.2079T>C (p.Phe693=)
7g.107710121T>GCA368845814SLC26A4c.2157T>G (p.Phe719Leu)
c.813T>G
n.377-34T>G
c.2079T>G (p.Phe693Leu)
7g.107710122T>ACA368845816SLC26A4c.2158T>A (p.Leu720Met)
c.814T>A
n.377-33T>A
c.2080T>A (p.Leu694Met)
7g.107710122T>CCA457104600SLC26A4c.2158T>C (p.Leu720=)
c.814T>C
n.377-33T>C
c.2080T>C (p.Leu694=)
7g.107710122T>GCA368845819SLC26A4c.2158T>G (p.Leu720Val)
c.814T>G
n.377-33T>G
c.2080T>G (p.Leu694Val)
7g.107710123T>ACA368845821SLC26A4c.2159T>A (p.Leu720Ter)
c.815T>A
n.377-32T>A
c.2081T>A (p.Leu694Ter)
7g.107710123T>CCA368845823SLC26A4c.2159T>C (p.Leu720Ser)
c.815T>C
n.377-32T>C
c.2081T>C (p.Leu694Ser)
 dbSNP gnomAD v3 gnomAD v4
7g.107710123T>GCA368845824SLC26A4c.2159T>G (p.Leu720Trp)
c.815T>G
n.377-32T>G
c.2081T>G (p.Leu694Trp)
7g.107710123T=CA1732751322SLC26A4c.2159T= (p.Leu720=)
c.815T=
n.377-32T=
c.2081T= (p.Leu694=)
7g.107710124G>ACA457104601SLC26A4c.2160G>A (p.Leu720=)
c.816G>A
n.377-31G>A
c.2082G>A (p.Leu694=)
7g.107710124G>CCA368845826SLC26A4c.2160G>C (p.Leu720Phe)
c.816G>C
n.377-31G>C
c.2082G>C (p.Leu694Phe)
7g.107710124G>TCA368845828SLC26A4c.2160G>T (p.Leu720Phe)
c.816G>T
n.377-31G>T
c.2082G>T (p.Leu694Phe)
7g.107710125A=CA1732751325SLC26A4c.2161A= (p.Thr721=)
c.817A=
n.377-30A=
c.2083A= (p.Thr695=)
7g.107710125A>CCA368845831SLC26A4c.2161A>C (p.Thr721Pro)
c.817A>C
n.377-30A>C
c.2083A>C (p.Thr695Pro)
7g.107710125A>GCA368845833SLC26A4c.2161A>G (p.Thr721Ala)
c.817A>G
n.377-30A>G
c.2083A>G (p.Thr695Ala)
 dbSNP gnomAD v3 gnomAD v4
7g.107710125A>TCA368845839SLC26A4c.2161A>T (p.Thr721Ser)
c.817A>T
n.377-30A>T
c.2083A>T (p.Thr695Ser)
7g.107710126delCA2684468644SLC26A4c.2162del (p.Thr721ArgfsTer13)
c.818del
n.377-29del
c.2084del (p.Thr695ArgfsTer13)
 gnomAD v4
7g.107710126C>ACA368845842SLC26A4c.2162C>A (p.Thr721Lys)
c.818C>A
n.377-29C>A
c.2084C>A (p.Thr695Lys)
 ClinVar dbSNP gnomAD v4
7g.107710126C=CA1732751328SLC26A4c.2162C= (p.Thr721=)
c.818C=
n.377-29C=
c.2084C= (p.Thr695=)
7g.107710126C>GCA368845843SLC26A4c.2162C>G (p.Thr721Arg)
c.818C>G
n.377-29C>G
c.2084C>G (p.Thr695Arg)
 gnomAD v4
7g.107710126C>TCA253308SLC26A4c.2162C>T (p.Thr721Met)
c.818C>T
n.377-29C>T
c.2084C>T (p.Thr695Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710127G>ACA4433061SLC26A4c.2163G>A (p.Thr721=)
c.819G>A
n.377-28G>A
c.2085G>A (p.Thr695=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710127G>CCA4433062SLC26A4c.2163G>C (p.Thr721=)
c.819G>C
n.377-28G>C
c.2085G>C (p.Thr695=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107710127G=CA1732751333SLC26A4c.2163G= (p.Thr721=)
c.819G=
n.377-28G=
c.2085G= (p.Thr695=)
7g.107710127G>TCA457104602SLC26A4c.2163G>T (p.Thr721=)
c.819G>T
n.377-28G>T
c.2085G>T (p.Thr695=)
 dbSNP gnomAD v2 gnomAD v4
7g.107710128G>ACA368845854SLC26A4c.2164G>A (p.Val722Ile)
c.820G>A
n.377-27G>A
c.2086G>A (p.Val696Ile)
 gnomAD v4
7g.107710128G>CCA368845855SLC26A4c.2164G>C (p.Val722Leu)
c.820G>C
n.377-27G>C
c.2086G>C (p.Val696Leu)
7g.107710128G>TCA368845856SLC26A4c.2164G>T (p.Val722Phe)
c.820G>T
n.377-27G>T
c.2086G>T (p.Val696Phe)
7g.107710129T>ACA368845858SLC26A4c.2165T>A (p.Val722Asp)
c.821T>A
n.377-26T>A
c.2087T>A (p.Val696Asp)
7g.107710129T>CCA368845861SLC26A4c.2165T>C (p.Val722Ala)
c.821T>C
n.377-26T>C
c.2087T>C (p.Val696Ala)
 COSMIC
7g.107710129T>GCA4433063SLC26A4c.2165T>G (p.Val722Gly)
c.821T>G
n.377-26T>G
c.2087T>G (p.Val696Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107710129T=CA1732751337SLC26A4c.2165T= (p.Val722=)
c.821T=
n.377-26T=
c.2087T= (p.Val696=)
7g.107710130C>ACA457104603SLC26A4c.2166C>A (p.Val722=)
c.822C>A
n.377-25C>A
c.2088C>A (p.Val696=)
 gnomAD v4
7g.107710130C>GCA457104604SLC26A4c.2166C>G (p.Val722=)
c.822C>G
n.377-25C>G
c.2088C>G (p.Val696=)
 ClinVar dbSNP
7g.107710130C>TCA457104605SLC26A4c.2166C>T (p.Val722=)
c.822C>T
n.377-25C>T
c.2088C>T (p.Val696=)
 gnomAD v4 COSMIC
7g.107710131C>ACA368845866SLC26A4c.2167C>A (p.His723Asn)
c.823C>A
n.377-24C>A
c.2089C>A (p.His697Asn)
 gnomAD v4
7g.107710131C=CA1732751339SLC26A4c.2167C= (p.His723=)
c.823C=
n.377-24C=
c.2089C= (p.His697=)
7g.107710131C>GCA368845871SLC26A4c.2167C>G (p.His723Asp)
c.823C>G
n.377-24C>G
c.2089C>G (p.His697Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107710131C>TCA368845869SLC26A4c.2167C>T (p.His723Tyr)
c.823C>T
n.377-24C>T
c.2089C>T (p.His697Tyr)
7g.107710132A=CA1732751341SLC26A4c.2168A= (p.His723=)
c.824A=
n.377-23A=
c.2090A= (p.His697=)
7g.107710132A>CCA368845873SLC26A4c.2168A>C (p.His723Pro)
c.824A>C
n.377-23A>C
c.2090A>C (p.His697Pro)
 gnomAD v4
7g.107710132A>GCA253307SLC26A4c.2168A>G (p.His723Arg)
c.824A>G
n.377-23A>G
c.2090A>G (p.His697Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.[107710132A>G;107715429C>G]CA2499306164SLC26A4c.[2168A>G;2326C>G] (p.[His723Arg;Arg776Gly])
c.[824A>G;982C>G]
n.[377-23A>G;512C>G]
c.[2090A>G;2248C>G] (p.[His697Arg;Arg750Gly])
7g.107710132A>TCA368845876SLC26A4c.2168A>T (p.His723Leu)
c.824A>T
n.377-23A>T
c.2090A>T (p.His697Leu)
 gnomAD v4
7g.107710133T>ACA368845878SLC26A4c.2169T>A (p.His723Gln)
c.825T>A
n.377-22T>A
c.2091T>A (p.His697Gln)
7g.107710133T>CCA457104606SLC26A4c.2169T>C (p.His723=)
c.825T>C
n.377-22T>C
c.2091T>C (p.His697=)
7g.107710133T>GCA368845880SLC26A4c.2169T>G (p.His723Gln)
c.825T>G
n.377-22T>G
c.2091T>G (p.His697Gln)
7g.107710134G>ACA164228112SLC26A4c.2170G>A (p.Asp724Asn)
c.826G>A
n.377-21G>A
c.2092G>A (p.Asp698Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107710134G>CCA368845883SLC26A4c.2170G>C (p.Asp724His)
c.826G>C
n.377-21G>C
c.2092G>C (p.Asp698His)
7g.107710134G=CA1732751342SLC26A4c.2170G= (p.Asp724=)
c.826G=
n.377-21G=
c.2092G= (p.Asp698=)
7g.107710134G>TCA368845885SLC26A4c.2170G>T (p.Asp724Tyr)
c.826G>T
n.377-21G>T
c.2092G>T (p.Asp698Tyr)
 gnomAD v4

Number of alleles fetched