Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149980661T>ACA361707079SLC26A2c.1068T>A (p.Tyr356Ter)
c.372+2310T>A (n.372+2310T>A)
5g.149980661T>CCA447402294SLC26A2c.1068T>C (p.Tyr356=)
c.372+2310T>C (n.372+2310T>C)
5g.149980661T>GCA361707080SLC26A2c.1068T>G (p.Tyr356Ter)
c.372+2310T>G (n.372+2310T>G)
5g.149980662A>CCA361707081SLC26A2c.1069A>C (p.Asn357His)
c.372+2311A>C (n.372+2311A>C)
5g.149980662A>GCA361707082SLC26A2c.1069A>G (p.Asn357Asp)
c.372+2311A>G (n.372+2311A>G)
gnomAD v4
5g.149980662A>TCA361707083SLC26A2c.1069A>T (p.Asn357Tyr)
c.372+2311A>T (n.372+2311A>T)
5g.149980663delCA2675943643SLC26A2c.1070del (p.Asn357IlefsTer22)
c.372+2312del (n.372+2312del)
gnomAD v4
5g.149980663A>CCA361707086SLC26A2c.1070A>C (p.Asn357Thr)
c.372+2312A>C (n.372+2312A>C)
5g.149980663A>GCA361707084SLC26A2c.1070A>G (p.Asn357Ser)
c.372+2312A>G (n.372+2312A>G)
5g.149980663A>TCA361707085SLC26A2c.1070A>T (p.Asn357Ile)
c.372+2312A>T (n.372+2312A>T)
5g.149980664T>ACA361707087SLC26A2c.1071T>A (p.Asn357Lys)
c.372+2313T>A (n.372+2313T>A)
5g.149980664T>CCA447402296SLC26A2c.1071T>C (p.Asn357=)
c.372+2313T>C (n.372+2313T>C)
5g.149980664T>GCA361707088SLC26A2c.1071T>G (p.Asn357Lys)
c.372+2313T>G (n.372+2313T>G)
5g.149980665T>ACA361707089SLC26A2c.1072T>A (p.Ser358Thr)
c.372+2314T>A (n.372+2314T>A)
5g.149980665T>CCA361707090SLC26A2c.1072T>C (p.Ser358Pro)
c.372+2314T>C (n.372+2314T>C)
5g.149980665T>GCA361707091SLC26A2c.1072T>G (p.Ser358Ala)
c.372+2314T>G (n.372+2314T>G)
5g.149980666C>ACA3505382SLC26A2c.1073C>A (p.Ser358Tyr)
c.372+2315C>A (n.372+2315C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.149980666C=CA1590738472SLC26A2c.1073C= (p.Ser358=)
c.372+2315C= (n.372+2315C=)
5g.149980666C>GCA361707092SLC26A2c.1073C>G (p.Ser358Cys)
c.372+2315C>G (n.372+2315C>G)
5g.149980666C>TCA361707093SLC26A2c.1073C>T (p.Ser358Phe)
c.372+2315C>T (n.372+2315C>T)
ClinVar dbSNP
5g.149980667T>ACA447402301SLC26A2c.1074T>A (p.Ser358=)
c.372+2316T>A (n.372+2316T>A)
5g.149980667T>CCA447402302SLC26A2c.1074T>C (p.Ser358=)
c.372+2316T>C (n.372+2316T>C)
5g.149980667T>GCA447402303SLC26A2c.1074T>G (p.Ser358=)
c.372+2316T>G (n.372+2316T>G)
5g.149980668A=CA1590738473SLC26A2c.1075A= (p.Ser359=)
c.372+2317A= (n.372+2317A=)
5g.149980668A>CCA361707094SLC26A2c.1075A>C (p.Ser359Arg)
c.372+2317A>C (n.372+2317A>C)
5g.149980668A>GCA361707095SLC26A2c.1075A>G (p.Ser359Gly)
c.372+2317A>G (n.372+2317A>G)
dbSNP
5g.149980668A>TCA361707096SLC26A2c.1075A>T (p.Ser359Cys)
c.372+2317A>T (n.372+2317A>T)
5g.149980669G>ACA361707099SLC26A2c.1076G>A (p.Ser359Asn)
c.372+2318G>A (n.372+2318G>A)
gnomAD v4
5g.149980669G>CCA361707098SLC26A2c.1076G>C (p.Ser359Thr)
c.372+2318G>C (n.372+2318G>C)
5g.149980669G>TCA361707097SLC26A2c.1076G>T (p.Ser359Ile)
c.372+2318G>T (n.372+2318G>T)
5g.149980670T>ACA361707100SLC26A2c.1077T>A (p.Ser359Arg)
c.372+2319T>A (n.372+2319T>A)
5g.149980670T>CCA447402305SLC26A2c.1077T>C (p.Ser359=)
c.372+2319T>C (n.372+2319T>C)
gnomAD v4
5g.149980670T>GCA361707101SLC26A2c.1077T>G (p.Ser359Arg)
c.372+2319T>G (n.372+2319T>G)
5g.149980671A>CCA361707102SLC26A2c.1078A>C (p.Ile360Leu)
c.372+2320A>C (n.372+2320A>C)
5g.149980671A>GCA361707103SLC26A2c.1078A>G (p.Ile360Val)
c.372+2320A>G (n.372+2320A>G)
gnomAD v4
5g.149980671A>TCA361707104SLC26A2c.1078A>T (p.Ile360Phe)
c.372+2320A>T (n.372+2320A>T)
5g.149980672T>ACA361707105SLC26A2c.1079T>A (p.Ile360Asn)
c.372+2321T>A (n.372+2321T>A)
5g.149980672T>CCA361707106SLC26A2c.1079T>C (p.Ile360Thr)
c.372+2321T>C (n.372+2321T>C)
gnomAD v4
5g.149980672T>GCA361707107SLC26A2c.1079T>G (p.Ile360Ser)
c.372+2321T>G (n.372+2321T>G)
5g.149980673T>ACA447402306SLC26A2c.1080T>A (p.Ile360=)
c.372+2322T>A (n.372+2322T>A)
5g.149980673T>CCA447402307SLC26A2c.1080T>C (p.Ile360=)
c.372+2322T>C (n.372+2322T>C)
5g.149980673T>GCA361707108SLC26A2c.1080T>G (p.Ile360Met)
c.372+2322T>G (n.372+2322T>G)
5g.149980674G>ACA3505383SLC26A2c.1081G>A (p.Ala361Thr)
c.372+2323G>A (n.372+2323G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149980674G>CCA361707109SLC26A2c.1081G>C (p.Ala361Pro)
c.372+2323G>C (n.372+2323G>C)
5g.149980674G=CA1590738474SLC26A2c.1081G= (p.Ala361=)
c.372+2323G= (n.372+2323G=)
5g.149980674G>TCA361707110SLC26A2c.1081G>T (p.Ala361Ser)
c.372+2323G>T (n.372+2323G>T)
gnomAD v4
5g.149980675C>ACA361707112SLC26A2c.1082C>A (p.Ala361Asp)
c.372+2324C>A (n.372+2324C>A)
5g.149980675C=CA1590738475SLC26A2c.1082C= (p.Ala361=)
c.372+2324C= (n.372+2324C=)
5g.149980675C>GCA361707113SLC26A2c.1082C>G (p.Ala361Gly)
c.372+2324C>G (n.372+2324C>G)
5g.149980675C>TCA361707111SLC26A2c.1082C>T (p.Ala361Val)
c.372+2324C>T (n.372+2324C>T)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched