Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.88139962C>A | CA357635037 | ABCG2 | c.34G>T (p.Val12Leu) c.88G>T (p.Val30Leu) c.148G>T (p.Val50Leu) | |
4 | g.88139962C= | CA1474620417 | ABCG2 | c.34G= (p.Val12=) c.88G= (p.Val30=) c.148G= (p.Val50=) | |
4 | g.88139962C>G | CA357635040 | ABCG2 | c.34G>C (p.Val12Leu) c.88G>C (p.Val30Leu) c.148G>C (p.Val50Leu) | |
4 | g.88139962C>T | CA129174 | ABCG2 | c.34G>A (p.Val12Met) c.88G>A (p.Val30Met) c.148G>A (p.Val50Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88139963T>A | CA440274490 | ABCG2 | c.33A>T (p.Pro11=) c.87A>T (p.Pro29=) c.147A>T (p.Pro49=) | dbSNP gnomAD v4 |
4 | g.88139963T>C | CA440274491 | ABCG2 | c.33A>G (p.Pro11=) c.87A>G (p.Pro29=) c.147A>G (p.Pro49=) | |
4 | g.88139963T>G | CA440274493 | ABCG2 | c.33A>C (p.Pro11=) c.87A>C (p.Pro29=) c.147A>C (p.Pro49=) | |
4 | g.88139963T= | CA1474620419 | ABCG2 | c.33A= (p.Pro11=) c.87A= (p.Pro29=) c.147A= (p.Pro49=) | |
4 | g.88139963_88139964delinsTG | CA1474620418 | ABCG2 | c.32_33delinsCA (p.Pro11=) c.86_87delinsCA (p.Pro29=) c.146_147delinsCA (p.Pro49=) | |
4 | g.88139964G>A | CA100894296 | ABCG2 | c.32C>T (p.Pro11Leu) c.86C>T (p.Pro29Leu) c.146C>T (p.Pro49Leu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.88139964G>C | CA357635045 | ABCG2 | c.32C>G (p.Pro11Arg) c.86C>G (p.Pro29Arg) c.146C>G (p.Pro49Arg) | |
4 | g.88139964G= | CA1474620420 | ABCG2 | c.32C= (p.Pro11=) c.86C= (p.Pro29=) c.146C= (p.Pro49=) | |
4 | g.88139964G>T | CA357635048 | ABCG2 | c.32C>A (p.Pro11Gln) c.86C>A (p.Pro29Gln) c.146C>A (p.Pro49Gln) | |
4 | g.88139966del | CA3005057 | ABCG2 | c.32del (p.Pro11GlnfsTer18) c.86del (p.Pro29GlnfsTer18) c.146del (p.Pro49GlnfsTer18) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.88139965G>A | CA357635050 | ABCG2 | c.31C>T (p.Pro11Ser) c.85C>T (p.Pro29Ser) c.145C>T (p.Pro49Ser) | |
4 | g.88139965G>C | CA357635051 | ABCG2 | c.31C>G (p.Pro11Ala) c.85C>G (p.Pro29Ala) c.145C>G (p.Pro49Ala) | |
4 | g.88139965G>T | CA357635053 | ABCG2 | c.31C>A (p.Pro11Thr) c.85C>A (p.Pro29Thr) c.145C>A (p.Pro49Thr) | |
4 | g.88139966G>A | CA440274515 | ABCG2 | c.30C>T (p.Ile10=) c.84C>T (p.Ile28=) c.144C>T (p.Ile48=) | COSMIC COSMIC |
4 | g.88139966G>C | CA357635055 | ABCG2 | c.30C>G (p.Ile10Met) c.84C>G (p.Ile28Met) c.144C>G (p.Ile48Met) | |
4 | g.88139966G= | CA1474620421 | ABCG2 | c.30C= (p.Ile10=) c.84C= (p.Ile28=) c.144C= (p.Ile48=) | |
4 | g.88139966G>T | CA440274519 | ABCG2 | c.30C>A (p.Ile10=) c.84C>A (p.Ile28=) c.144C>A (p.Ile48=) | dbSNP |
4 | g.88139967A>C | CA357635057 | ABCG2 | c.29T>G (p.Ile10Ser) c.83T>G (p.Ile28Ser) c.143T>G (p.Ile48Ser) | |
4 | g.88139967A>G | CA357635059 | ABCG2 | c.29T>C (p.Ile10Thr) c.83T>C (p.Ile28Thr) c.143T>C (p.Ile48Thr) | |
4 | g.88139967A>T | CA357635062 | ABCG2 | c.29T>A (p.Ile10Asn) c.83T>A (p.Ile28Asn) c.143T>A (p.Ile48Asn) | |
4 | g.88139968T>A | CA357635065 | ABCG2 | c.28A>T (p.Ile10Phe) c.82A>T (p.Ile28Phe) c.142A>T (p.Ile48Phe) | |
4 | g.88139968T>C | CA357635067 | ABCG2 | c.28A>G (p.Ile10Val) c.82A>G (p.Ile28Val) c.142A>G (p.Ile48Val) | |
4 | g.88139968T>G | CA357635068 | ABCG2 | c.28A>C (p.Ile10Leu) c.82A>C (p.Ile28Leu) c.142A>C (p.Ile48Leu) | |
4 | g.88139969A>C | CA357635071 | ABCG2 | c.27T>G (p.Phe9Leu) c.81T>G (p.Phe27Leu) c.141T>G (p.Phe47Leu) | |
4 | g.88139969A>G | CA440274526 | ABCG2 | c.27T>C (p.Phe9=) c.81T>C (p.Phe27=) c.141T>C (p.Phe47=) | |
4 | g.88139969A>T | CA357635073 | ABCG2 | c.27T>A (p.Phe9Leu) c.81T>A (p.Phe27Leu) c.141T>A (p.Phe47Leu) | |
4 | g.88139970A>C | CA357635079 | ABCG2 | c.26T>G (p.Phe9Cys) c.80T>G (p.Phe27Cys) c.140T>G (p.Phe47Cys) | |
4 | g.88139970A>G | CA357635077 | ABCG2 | c.26T>C (p.Phe9Ser) c.80T>C (p.Phe27Ser) c.140T>C (p.Phe47Ser) | |
4 | g.88139970A>T | CA357635076 | ABCG2 | c.26T>A (p.Phe9Tyr) c.80T>A (p.Phe27Tyr) c.140T>A (p.Phe47Tyr) | |
4 | g.88139971A>C | CA357635082 | ABCG2 | c.25T>G (p.Phe9Val) c.79T>G (p.Phe27Val) c.139T>G (p.Phe47Val) | |
4 | g.88139971A>G | CA357635083 | ABCG2 | c.25T>C (p.Phe9Leu) c.79T>C (p.Phe27Leu) c.139T>C (p.Phe47Leu) | |
4 | g.88139971A>T | CA357635085 | ABCG2 | c.25T>A (p.Phe9Ile) c.79T>A (p.Phe27Ile) c.139T>A (p.Phe47Ile) | |
4 | g.88139972A= | CA1474620422 | ABCG2 | c.24T= (p.Val8=) c.78T= (p.Val26=) c.138T= (p.Val46=) | |
4 | g.88139972A>C | CA440274533 | ABCG2 | c.24T>G (p.Val8=) c.78T>G (p.Val26=) c.138T>G (p.Val46=) | |
4 | g.88139972A>G | CA440274535 | ABCG2 | c.24T>C (p.Val8=) c.78T>C (p.Val26=) c.138T>C (p.Val46=) | |
4 | g.88139972A>T | CA440274537 | ABCG2 | c.24T>A (p.Val8=) c.78T>A (p.Val26=) c.138T>A (p.Val46=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.88139973A= | CA1474620423 | ABCG2 | c.23T= (p.Val8=) c.77T= (p.Val26=) c.137T= (p.Val46=) | |
4 | g.88139973A>C | CA357635087 | ABCG2 | c.23T>G (p.Val8Gly) c.77T>G (p.Val26Gly) c.137T>G (p.Val46Gly) | dbSNP gnomAD v4 |
4 | g.88139973A>G | CA3005058 | ABCG2 | c.23T>C (p.Val8Ala) c.77T>C (p.Val26Ala) c.137T>C (p.Val46Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88139973A>T | CA357635090 | ABCG2 | c.23T>A (p.Val8Asp) c.77T>A (p.Val26Asp) c.137T>A (p.Val46Asp) | |
4 | g.88139974C>A | CA357635092 | ABCG2 | c.22G>T (p.Val8Phe) c.76G>T (p.Val26Phe) c.136G>T (p.Val46Phe) | dbSNP gnomAD v4 |
4 | g.88139974C= | CA1474620424 | ABCG2 | c.22G= (p.Val8=) c.76G= (p.Val26=) c.136G= (p.Val46=) | |
4 | g.88139974C>G | CA357635095 | ABCG2 | c.22G>C (p.Val8Leu) c.76G>C (p.Val26Leu) c.136G>C (p.Val46Leu) | |
4 | g.88139974C>T | CA3005059 | ABCG2 | c.22G>A (p.Val8Ile) c.76G>A (p.Val26Ile) c.136G>A (p.Val46Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.88139975T>A | CA357635098 | ABCG2 | c.21A>T (p.Glu7Asp) c.75A>T (p.Glu25Asp) c.135A>T (p.Glu45Asp) | |
4 | g.88139975T>C | CA440274549 | ABCG2 | c.21A>G (p.Glu7=) c.75A>G (p.Glu25=) c.135A>G (p.Glu45=) | gnomAD v4 |