Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.99851537G>ACA5644184ABCC2c.4544G>A (p.Cys1515Tyr)
c.614G>A
c.3848G>A (p.Cys1283Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.99851537G>CCA378130687ABCC2c.4544G>C (p.Cys1515Ser)
c.614G>C
c.3848G>C (p.Cys1283Ser)
10g.99851537G=CA1931484653ABCC2c.4544G= (p.Cys1515=)
c.614G=
c.3848G= (p.Cys1283=)
10g.99851537G>TCA378130688ABCC2c.4544G>T (p.Cys1515Phe)
c.614G>T
c.3848G>T (p.Cys1283Phe)
10g.99851538C>ACA378130692ABCC2c.4545C>A (p.Cys1515Ter)
c.615C>A
c.3849C>A (p.Cys1283Ter)
10g.99851538C=CA1931484663ABCC2c.4545C= (p.Cys1515=)
c.615C=
c.3849C= (p.Cys1283=)
10g.99851538C>GCA378130690ABCC2c.4545C>G (p.Cys1515Trp)
c.615C>G
c.3849C>G (p.Cys1283Trp)
10g.99851538C>TCA5644185ABCC2c.4545C>T (p.Cys1515=)
c.615C>T
c.3849C>T (p.Cys1283=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.99851539G>ACA5644186ABCC2c.4546G>A (p.Gly1516Ser)
c.616G>A
c.3850G>A (p.Gly1284Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.99851539G>CCA378130695ABCC2c.4546G>C (p.Gly1516Arg)
c.616G>C
c.3850G>C (p.Gly1284Arg)
10g.99851539G=CA1931484667ABCC2c.4546G= (p.Gly1516=)
c.616G=
c.3850G= (p.Gly1284=)
10g.99851539G>TCA378130698ABCC2c.4546G>T (p.Gly1516Cys)
c.616G>T
c.3850G>T (p.Gly1284Cys)
10g.99851540G>ACA378130701ABCC2c.4547G>A (p.Gly1516Asp)
c.617G>A
c.3851G>A (p.Gly1284Asp)
dbSNP gnomAD v4
10g.99851540G>CCA378130702ABCC2c.4547G>C (p.Gly1516Ala)
c.617G>C
c.3851G>C (p.Gly1284Ala)
10g.99851540G>TCA378130704ABCC2c.4547G>T (p.Gly1516Val)
c.617G>T
c.3851G>T (p.Gly1284Val)
10g.99851541C>ACA471136052ABCC2c.4548C>A (p.Gly1516=)
c.618C>A
c.3852C>A (p.Gly1284=)
10g.99851541C>GCA471136053ABCC2c.4548C>G (p.Gly1516=)
c.618C>G
c.3852C>G (p.Gly1284=)
10g.99851541C>TCA471136054ABCC2c.4548C>T (p.Gly1516=)
c.618C>T
c.3852C>T (p.Gly1284=)
10g.99851542A>CCA378130706ABCC2c.4549A>C (p.Ser1517Arg)
c.619A>C
c.3853A>C (p.Ser1285Arg)
10g.99851542A>GCA378130711ABCC2c.4549A>G (p.Ser1517Gly)
c.619A>G
c.3853A>G (p.Ser1285Gly)
10g.99851542A>TCA378130709ABCC2c.4549A>T (p.Ser1517Cys)
c.619A>T
c.3853A>T (p.Ser1285Cys)
10g.99851543G>ACA378130713ABCC2c.4550G>A (p.Ser1517Asn)
c.620G>A
c.3854G>A (p.Ser1285Asn)
dbSNP
10g.99851543G>CCA378130714ABCC2c.4550G>C (p.Ser1517Thr)
c.620G>C
c.3854G>C (p.Ser1285Thr)
10g.99851543G>TCA378130717ABCC2c.4550G>T (p.Ser1517Ile)
c.620G>T
c.3854G>T (p.Ser1285Ile)
gnomAD v4
10g.99851544C>ACA378130719ABCC2c.4551C>A (p.Ser1517Arg)
c.621C>A
c.3855C>A (p.Ser1285Arg)
10g.99851544C>GCA378130722ABCC2c.4551C>G (p.Ser1517Arg)
c.621C>G
c.3855C>G (p.Ser1285Arg)
10g.99851544C>TCA471136055ABCC2c.4551C>T (p.Ser1517=)
c.621C>T
c.3855C>T (p.Ser1285=)
dbSNP
10g.99851545C>ACA378130725ABCC2c.4552C>A (p.Pro1518Thr)
c.622C>A
c.3856C>A (p.Pro1286Thr)
10g.99851545C>GCA378130727ABCC2c.4552C>G (p.Pro1518Ala)
c.622C>G
c.3856C>G (p.Pro1286Ala)
gnomAD v4
10g.99851545C>TCA378130728ABCC2c.4552C>T (p.Pro1518Ser)
c.622C>T
c.3856C>T (p.Pro1286Ser)
gnomAD v4
10g.99851546C>ACA378130730ABCC2c.4553C>A (p.Pro1518His)
c.623C>A
c.3857C>A (p.Pro1286His)
10g.99851546C=CA1931484673ABCC2c.4553C= (p.Pro1518=)
c.623C=
c.3857C= (p.Pro1286=)
10g.99851546C>GCA5644187ABCC2c.4553C>G (p.Pro1518Arg)
c.623C>G
c.3857C>G (p.Pro1286Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.99851546C>TCA378130734ABCC2c.4553C>T (p.Pro1518Leu)
c.623C>T
c.3857C>T (p.Pro1286Leu)
10g.99851547T>ACA471136058ABCC2c.4554T>A (p.Pro1518=)
c.624T>A
c.3858T>A (p.Pro1286=)
10g.99851547T>CCA471136057ABCC2c.4554T>C (p.Pro1518=)
c.624T>C
c.3858T>C (p.Pro1286=)
10g.99851547T>GCA471136056ABCC2c.4554T>G (p.Pro1518=)
c.624T>G
c.3858T>G (p.Pro1286=)
10g.99851548G>ACA378130737ABCC2c.4555G>A (p.Glu1519Lys)
c.625G>A
c.3859G>A (p.Glu1287Lys)
ClinVar dbSNP
10g.99851548G>CCA378130741ABCC2c.4555G>C (p.Glu1519Gln)
c.625G>C
c.3859G>C (p.Glu1287Gln)
10g.99851548G=CA1931484683ABCC2c.4555G= (p.Glu1519=)
c.625G=
c.3859G= (p.Glu1287=)
10g.99851548G>TCA378130739ABCC2c.4555G>T (p.Glu1519Ter)
c.625G>T
c.3859G>T (p.Glu1287Ter)
10g.99851549A>CCA378130743ABCC2c.4556A>C (p.Glu1519Ala)
c.626A>C
c.3860A>C (p.Glu1287Ala)
10g.99851549A>GCA378130746ABCC2c.4556A>G (p.Glu1519Gly)
c.626A>G
c.3860A>G (p.Glu1287Gly)
gnomAD v4
10g.99851549A>TCA378130745ABCC2c.4556A>T (p.Glu1519Val)
c.626A>T
c.3860A>T (p.Glu1287Val)
10g.99851550A=CA1931484698ABCC2c.4557A= (p.Glu1519=)
c.627A=
c.3861A= (p.Glu1287=)
10g.99851550A>CCA5644188ABCC2c.4557A>C (p.Glu1519Asp)
c.627A>C
c.3861A>C (p.Glu1287Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.99851550A>GCA471136059ABCC2c.4557A>G (p.Glu1519=)
c.627A>G
c.3861A>G (p.Glu1287=)
10g.99851550A>TCA378130749ABCC2c.4557A>T (p.Glu1519Asp)
c.627A>T
c.3861A>T (p.Glu1287Asp)
10g.99851551G>ACA212872977ABCC2c.4558G>A (p.Glu1520Lys)
c.628G>A
c.3862G>A (p.Glu1288Lys)
dbSNP
10g.99851551G>CCA378130750ABCC2c.4558G>C (p.Glu1520Gln)
c.628G>C
c.3862G>C (p.Glu1288Gln)

Number of alleles fetched