Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.120738874C>A | CA6831152 | ACADS | c.988C>A (p.Arg330Ser) c.976C>A (p.Arg326Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.120738874C= | CA2067555555 | ACADS | c.988C= (p.Arg330=) c.976C= (p.Arg326=) | |
12 | g.120738874C>G | CA386601526 | ACADS | c.988C>G (p.Arg330Gly) c.976C>G (p.Arg326Gly) | |
12 | g.120738874C>T | CA312222 | ACADS | c.988C>T (p.Arg330Cys) c.976C>T (p.Arg326Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.120738874_120738876delinsCGC | CA2067555556 | ACADS | c.988_990delinsCGC (p.Arg330=) c.976_978delinsCGC (p.Arg326=) | |
12 | g.120738874_120738876delinsTGT | CA312246 | ACADS | c.988_990delinsTGT (p.Arg330Cys) c.976_978delinsTGT (p.Arg326Cys) | ClinVar dbSNP |
12 | g.120738875G>A | CA6831153 | ACADS | c.989G>A (p.Arg330His) c.977G>A (p.Arg326His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.120738875G>C | CA6831154 | ACADS | c.989G>C (p.Arg330Pro) c.977G>C (p.Arg326Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.120738875G= | CA2067555557 | ACADS | c.989G= (p.Arg330=) c.977G= (p.Arg326=) | |
12 | g.120738875G>T | CA386601527 | ACADS | c.989G>T (p.Arg330Leu) c.977G>T (p.Arg326Leu) | |
12 | g.120738875_120738876delinsAT | CA645372922 | ACADS | c.989_990delinsAT (p.Arg330His) c.977_978delinsAT (p.Arg326His) | ClinVar dbSNP |
12 | g.120738875_120738876delinsGC | CA2067555558 | ACADS | c.989_990delinsGC (p.Arg330=) c.977_978delinsGC (p.Arg326=) | |
12 | g.120738875_120738876delinsTT | CA2739277338 | ACADS | c.989_990delinsTT (p.Arg330Leu) c.977_978delinsTT (p.Arg326Leu) | ClinVar |
12 | g.120738876C>A | CA244494714 | ACADS | c.990C>A (p.Arg330=) c.978C>A (p.Arg326=) | dbSNP |
12 | g.120738876C= | CA2067555559 | ACADS | c.990C= (p.Arg330=) c.978C= (p.Arg326=) | |
12 | g.120738876C>G | CA244494717 | ACADS | c.990C>G (p.Arg330=) c.978C>G (p.Arg326=) | |
12 | g.120738876C>T | CA289255 | ACADS | c.990C>T (p.Arg330=) c.978C>T (p.Arg326=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.120738877G>A | CA386601528 | ACADS | c.991G>A (p.Ala331Thr) c.979G>A (p.Ala327Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.120738877G>C | CA386601529 | ACADS | c.991G>C (p.Ala331Pro) c.979G>C (p.Ala327Pro) | |
12 | g.120738877G= | CA2067555560 | ACADS | c.991G= (p.Ala331=) c.979G= (p.Ala327=) | |
12 | g.120738877G>T | CA386601530 | ACADS | c.991G>T (p.Ala331Ser) c.979G>T (p.Ala327Ser) | |
12 | g.120738878C>A | CA386601531 | ACADS | c.992C>A (p.Ala331Asp) c.980C>A (p.Ala327Asp) | gnomAD v3 gnomAD v4 |
12 | g.120738878C= | CA2067555561 | ACADS | c.992C= (p.Ala331=) c.980C= (p.Ala327=) | |
12 | g.120738878C>G | CA386601532 | ACADS | c.992C>G (p.Ala331Gly) c.980C>G (p.Ala327Gly) | |
12 | g.120738878C>T | CA386601533 | ACADS | c.992C>T (p.Ala331Val) c.980C>T (p.Ala327Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.120738879T>A | CA482146809 | ACADS | c.993T>A (p.Ala331=) c.981T>A (p.Ala327=) | |
12 | g.120738879T>C | CA6831155 | ACADS | c.993T>C (p.Ala331=) c.981T>C (p.Ala327=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.120738879T>G | CA482146810 | ACADS | c.993T>G (p.Ala331=) c.981T>G (p.Ala327=) | |
12 | g.120738879T= | CA2067555562 | ACADS | c.993T= (p.Ala331=) c.981T= (p.Ala327=) | |
12 | g.120738880G>A | CA6831156 | ACADS | c.994G>A (p.Ala332Thr) c.982G>A (p.Ala328Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.120738880G>C | CA386601534 | ACADS | c.994G>C (p.Ala332Pro) c.982G>C (p.Ala328Pro) | |
12 | g.120738880G= | CA2067555563 | ACADS | c.994G= (p.Ala332=) c.982G= (p.Ala328=) | |
12 | g.120738880G>T | CA386601535 | ACADS | c.994G>T (p.Ala332Ser) c.982G>T (p.Ala328Ser) | |
12 | g.120738881C>A | CA386601536 | ACADS | c.995C>A (p.Ala332Asp) c.983C>A (p.Ala328Asp) | |
12 | g.120738881C= | CA2067555564 | ACADS | c.995C= (p.Ala332=) c.983C= (p.Ala328=) | |
12 | g.120738881C>G | CA386601537 | ACADS | c.995C>G (p.Ala332Gly) c.983C>G (p.Ala328Gly) | |
12 | g.120738881C>T | CA386601538 | ACADS | c.995C>T (p.Ala332Val) c.983C>T (p.Ala328Val) | ClinVar dbSNP gnomAD v4 |
12 | g.120738882C>A | CA482146817 | ACADS | c.996C>A (p.Ala332=) c.984C>A (p.Ala328=) | gnomAD v4 |
12 | g.120738882C>G | CA482146819 | ACADS | c.996C>G (p.Ala332=) c.984C>G (p.Ala328=) | |
12 | g.120738882C>T | CA482146820 | ACADS | c.996C>T (p.Ala332=) c.984C>T (p.Ala328=) | |
12 | g.120738883A>C | CA386601539 | ACADS | c.997A>C (p.Met333Leu) c.985A>C (p.Met329Leu) | |
12 | g.120738883A>G | CA386601540 | ACADS | c.997A>G (p.Met333Val) c.985A>G (p.Met329Val) | |
12 | g.120738883A>T | CA386601541 | ACADS | c.997A>T (p.Met333Leu) c.985A>T (p.Met329Leu) | gnomAD v4 |
12 | g.120738884T>A | CA386601542 | ACADS | c.998T>A (p.Met333Lys) c.986T>A (p.Met329Lys) | |
12 | g.120738884T>C | CA386601543 | ACADS | c.998T>C (p.Met333Thr) c.986T>C (p.Met329Thr) | |
12 | g.120738884T>G | CA386601544 | ACADS | c.998T>G (p.Met333Arg) c.986T>G (p.Met329Arg) | |
12 | g.120738885G>A | CA386601545 | ACADS | c.999G>A (p.Met333Ile) c.987G>A (p.Met329Ile) | |
12 | g.120738885G>C | CA386601546 | ACADS | c.999G>C (p.Met333Ile) c.987G>C (p.Met329Ile) | |
12 | g.120738885G>T | CA386601547 | ACADS | c.999G>T (p.Met333Ile) c.987G>T (p.Met329Ile) | |
12 | g.120738886C>A | CA386601548 | ACADS | c.1000C>A (p.Leu334Met) c.988C>A (p.Leu330Met) |