Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.149980663del | CA2675943643 | SLC26A2 | c.1070del (p.Asn357IlefsTer22) c.372+2312del (n.372+2312del) | gnomAD v4 |
5 | g.149980663A>C | CA361707086 | SLC26A2 | c.1070A>C (p.Asn357Thr) c.372+2312A>C (n.372+2312A>C) | |
5 | g.149980663A>G | CA361707084 | SLC26A2 | c.1070A>G (p.Asn357Ser) c.372+2312A>G (n.372+2312A>G) | |
5 | g.149980663A>T | CA361707085 | SLC26A2 | c.1070A>T (p.Asn357Ile) c.372+2312A>T (n.372+2312A>T) | |
5 | g.149980664T>A | CA361707087 | SLC26A2 | c.1071T>A (p.Asn357Lys) c.372+2313T>A (n.372+2313T>A) | |
5 | g.149980664T>C | CA447402296 | SLC26A2 | c.1071T>C (p.Asn357=) c.372+2313T>C (n.372+2313T>C) | |
5 | g.149980664T>G | CA361707088 | SLC26A2 | c.1071T>G (p.Asn357Lys) c.372+2313T>G (n.372+2313T>G) | |
5 | g.149980665T>A | CA361707089 | SLC26A2 | c.1072T>A (p.Ser358Thr) c.372+2314T>A (n.372+2314T>A) | |
5 | g.149980665T>C | CA361707090 | SLC26A2 | c.1072T>C (p.Ser358Pro) c.372+2314T>C (n.372+2314T>C) | |
5 | g.149980665T>G | CA361707091 | SLC26A2 | c.1072T>G (p.Ser358Ala) c.372+2314T>G (n.372+2314T>G) | |
5 | g.149980666C>A | CA3505382 | SLC26A2 | c.1073C>A (p.Ser358Tyr) c.372+2315C>A (n.372+2315C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149980666C= | CA1590738472 | SLC26A2 | c.1073C= (p.Ser358=) c.372+2315C= (n.372+2315C=) | |
5 | g.149980666C>G | CA361707092 | SLC26A2 | c.1073C>G (p.Ser358Cys) c.372+2315C>G (n.372+2315C>G) | |
5 | g.149980666C>T | CA361707093 | SLC26A2 | c.1073C>T (p.Ser358Phe) c.372+2315C>T (n.372+2315C>T) | ClinVar dbSNP |
5 | g.149980667T>A | CA447402301 | SLC26A2 | c.1074T>A (p.Ser358=) c.372+2316T>A (n.372+2316T>A) | |
5 | g.149980667T>C | CA447402302 | SLC26A2 | c.1074T>C (p.Ser358=) c.372+2316T>C (n.372+2316T>C) | |
5 | g.149980667T>G | CA447402303 | SLC26A2 | c.1074T>G (p.Ser358=) c.372+2316T>G (n.372+2316T>G) | |
5 | g.149980668A= | CA1590738473 | SLC26A2 | c.1075A= (p.Ser359=) c.372+2317A= (n.372+2317A=) | |
5 | g.149980668A>C | CA361707094 | SLC26A2 | c.1075A>C (p.Ser359Arg) c.372+2317A>C (n.372+2317A>C) | |
5 | g.149980668A>G | CA361707095 | SLC26A2 | c.1075A>G (p.Ser359Gly) c.372+2317A>G (n.372+2317A>G) | dbSNP |
5 | g.149980668A>T | CA361707096 | SLC26A2 | c.1075A>T (p.Ser359Cys) c.372+2317A>T (n.372+2317A>T) | |
5 | g.149980669G>A | CA361707099 | SLC26A2 | c.1076G>A (p.Ser359Asn) c.372+2318G>A (n.372+2318G>A) | gnomAD v4 |
5 | g.149980669G>C | CA361707098 | SLC26A2 | c.1076G>C (p.Ser359Thr) c.372+2318G>C (n.372+2318G>C) | |
5 | g.149980669G>T | CA361707097 | SLC26A2 | c.1076G>T (p.Ser359Ile) c.372+2318G>T (n.372+2318G>T) | |
5 | g.149980670T>A | CA361707100 | SLC26A2 | c.1077T>A (p.Ser359Arg) c.372+2319T>A (n.372+2319T>A) | |
5 | g.149980670T>C | CA447402305 | SLC26A2 | c.1077T>C (p.Ser359=) c.372+2319T>C (n.372+2319T>C) | gnomAD v4 |
5 | g.149980670T>G | CA361707101 | SLC26A2 | c.1077T>G (p.Ser359Arg) c.372+2319T>G (n.372+2319T>G) | |
5 | g.149980671A>C | CA361707102 | SLC26A2 | c.1078A>C (p.Ile360Leu) c.372+2320A>C (n.372+2320A>C) | |
5 | g.149980671A>G | CA361707103 | SLC26A2 | c.1078A>G (p.Ile360Val) c.372+2320A>G (n.372+2320A>G) | gnomAD v4 |
5 | g.149980671A>T | CA361707104 | SLC26A2 | c.1078A>T (p.Ile360Phe) c.372+2320A>T (n.372+2320A>T) | |
5 | g.149980672T>A | CA361707105 | SLC26A2 | c.1079T>A (p.Ile360Asn) c.372+2321T>A (n.372+2321T>A) | |
5 | g.149980672T>C | CA361707106 | SLC26A2 | c.1079T>C (p.Ile360Thr) c.372+2321T>C (n.372+2321T>C) | gnomAD v4 |
5 | g.149980672T>G | CA361707107 | SLC26A2 | c.1079T>G (p.Ile360Ser) c.372+2321T>G (n.372+2321T>G) | |
5 | g.149980673T>A | CA447402306 | SLC26A2 | c.1080T>A (p.Ile360=) c.372+2322T>A (n.372+2322T>A) | |
5 | g.149980673T>C | CA447402307 | SLC26A2 | c.1080T>C (p.Ile360=) c.372+2322T>C (n.372+2322T>C) | |
5 | g.149980673T>G | CA361707108 | SLC26A2 | c.1080T>G (p.Ile360Met) c.372+2322T>G (n.372+2322T>G) | |
5 | g.149980674G>A | CA3505383 | SLC26A2 | c.1081G>A (p.Ala361Thr) c.372+2323G>A (n.372+2323G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149980674G>C | CA361707109 | SLC26A2 | c.1081G>C (p.Ala361Pro) c.372+2323G>C (n.372+2323G>C) | |
5 | g.149980674G= | CA1590738474 | SLC26A2 | c.1081G= (p.Ala361=) c.372+2323G= (n.372+2323G=) | |
5 | g.149980674G>T | CA361707110 | SLC26A2 | c.1081G>T (p.Ala361Ser) c.372+2323G>T (n.372+2323G>T) | gnomAD v4 |
5 | g.149980675C>A | CA361707112 | SLC26A2 | c.1082C>A (p.Ala361Asp) c.372+2324C>A (n.372+2324C>A) | |
5 | g.149980675C= | CA1590738475 | SLC26A2 | c.1082C= (p.Ala361=) c.372+2324C= (n.372+2324C=) | |
5 | g.149980675C>G | CA361707113 | SLC26A2 | c.1082C>G (p.Ala361Gly) c.372+2324C>G (n.372+2324C>G) | |
5 | g.149980675C>T | CA361707111 | SLC26A2 | c.1082C>T (p.Ala361Val) c.372+2324C>T (n.372+2324C>T) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.149980676T>A | CA447402312 | SLC26A2 | c.1083T>A (p.Ala361=) c.372+2325T>A (n.372+2325T>A) | |
5 | g.149980676T>C | CA447402315 | SLC26A2 | c.1083T>C (p.Ala361=) c.372+2325T>C (n.372+2325T>C) | |
5 | g.149980676T>G | CA447402313 | SLC26A2 | c.1083T>G (p.Ala361=) c.372+2325T>G (n.372+2325T>G) | |
5 | g.149980677G>A | CA361707114 | SLC26A2 | c.1084G>A (p.Gly362Arg) c.372+2326G>A (n.372+2326G>A) | |
5 | g.149980677G>C | CA361707115 | SLC26A2 | c.1084G>C (p.Gly362Arg) c.372+2326G>C (n.372+2326G>C) | |
5 | g.149980677G>T | CA361707116 | SLC26A2 | c.1084G>T (p.Gly362Ter) c.372+2326G>T (n.372+2326G>T) |