Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.47566713_47566728delinsGCTCCACGTCCACTCC | CA2427968727 | ARAF | c.632_647delinsGCTCCACGTCCACTCC (p.Arg211=) c.641_656delinsGCTCCACGTCCACTCC (p.Arg214=) c.647_662delinsGCTCCACGTCCACTCC (p.Arg216=) c.-26_-11delinsGCTCCACGTCCACTCC (n.-26_-11delinsGCTCCACGTCCACTCC) | |
X | g.47566715_47566729del | CA875843492 | ARAF | c.634_648del (p.Ser212_Pro216del) c.643_657del (p.Ser215_Pro219del) c.649_663del (p.Ser217_Pro221del) c.-24_-10del (n.-24_-10del) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47566721T>A | CA412813391 | ARAF | c.640T>A (p.Ser214Thr) c.649T>A (p.Ser217Thr) c.655T>A (p.Ser219Thr) c.-18T>A (n.-18T>A) | dbSNP COSMIC |
X | g.47566721T>C | CA412813392 | ARAF | c.640T>C (p.Ser214Pro) c.649T>C (p.Ser217Pro) c.655T>C (p.Ser219Pro) c.-18T>C (n.-18T>C) | |
X | g.47566721T>G | CA16602806 | ARAF | c.640T>G (p.Ser214Ala) c.649T>G (p.Ser217Ala) c.655T>G (p.Ser219Ala) c.-18T>G (n.-18T>G) | ClinVar dbSNP COSMIC |
X | g.47566721T= | CA2427968730 | ARAF | c.640T= (p.Ser214=) c.649T= (p.Ser217=) c.655T= (p.Ser219=) c.-18T= (n.-18T=) | |
X | g.47566722C>A | CA412813393 | ARAF | c.641C>A (p.Ser214Tyr) c.650C>A (p.Ser217Tyr) c.656C>A (p.Ser219Tyr) c.-17C>A (n.-17C>A) | dbSNP COSMIC |
X | g.47566722C= | CA2427968731 | ARAF | c.641C= (p.Ser214=) c.650C= (p.Ser217=) c.656C= (p.Ser219=) c.-17C= (n.-17C=) | |
X | g.47566722C>G | CA16602595 | ARAF | c.641C>G (p.Ser214Cys) c.650C>G (p.Ser217Cys) c.656C>G (p.Ser219Cys) c.-17C>G (n.-17C>G) | ClinVar dbSNP COSMIC |
X | g.47566722C>T | CA16602805 | ARAF | c.641C>T (p.Ser214Phe) c.650C>T (p.Ser217Phe) c.656C>T (p.Ser219Phe) c.-17C>T (n.-17C>T) | ClinVar dbSNP gnomAD v4 COSMIC |
X | g.47566722_47566723delinsGT | CA645603172 | ARAF | c.641_642delinsGT (p.Ser214Cys) c.650_651delinsGT (p.Ser217Cys) c.656_657delinsGT (p.Ser219Cys) c.-17_-16delinsGT (n.-17_-16delinsGT) | COSMIC |
X | g.47566723C>A | CA10398056 | ARAF | c.642C>A (p.Ser214=) c.651C>A (p.Ser217=) c.657C>A (p.Ser219=) c.-16C>A (n.-16C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47566723C= | CA2427968732 | ARAF | c.642C= (p.Ser214=) c.651C= (p.Ser217=) c.657C= (p.Ser219=) c.-16C= (n.-16C=) | |
X | g.47566723C>G | CA515989177 | ARAF | c.642C>G (p.Ser214=) c.651C>G (p.Ser217=) c.657C>G (p.Ser219=) c.-16C>G (n.-16C>G) | gnomAD v4 |
X | g.47566723C>T | CA515989176 | ARAF | c.642C>T (p.Ser214=) c.651C>T (p.Ser217=) c.657C>T (p.Ser219=) c.-16C>T (n.-16C>T) | dbSNP |
X | g.47566724A>C | CA412813394 | ARAF | c.643A>C (p.Thr215Pro) c.652A>C (p.Thr218Pro) c.658A>C (p.Thr220Pro) c.-15A>C (n.-15A>C) | |
X | g.47566724A>G | CA412813395 | ARAF | c.643A>G (p.Thr215Ala) c.652A>G (p.Thr218Ala) c.658A>G (p.Thr220Ala) c.-15A>G (n.-15A>G) | |
X | g.47566724A>T | CA412813396 | ARAF | c.643A>T (p.Thr215Ser) c.652A>T (p.Thr218Ser) c.658A>T (p.Thr220Ser) c.-15A>T (n.-15A>T) | |
X | g.47566725C>A | CA412813399 | ARAF | c.644C>A (p.Thr215Asn) c.653C>A (p.Thr218Asn) c.659C>A (p.Thr220Asn) c.-14C>A (n.-14C>A) | |
X | g.47566725C>G | CA412813398 | ARAF | c.644C>G (p.Thr215Ser) c.653C>G (p.Thr218Ser) c.659C>G (p.Thr220Ser) c.-14C>G (n.-14C>G) | |
X | g.47566725C>T | CA412813397 | ARAF | c.644C>T (p.Thr215Ile) c.653C>T (p.Thr218Ile) c.659C>T (p.Thr220Ile) c.-14C>T (n.-14C>T) | dbSNP |
X | g.47566726T>A | CA515989183 | ARAF | c.645T>A (p.Thr215=) c.654T>A (p.Thr218=) c.660T>A (p.Thr220=) c.-13T>A (n.-13T>A) | |
X | g.47566726T>C | CA515989184 | ARAF | c.645T>C (p.Thr215=) c.654T>C (p.Thr218=) c.660T>C (p.Thr220=) c.-13T>C (n.-13T>C) | |
X | g.47566726T>G | CA515989185 | ARAF | c.645T>G (p.Thr215=) c.654T>G (p.Thr218=) c.660T>G (p.Thr220=) c.-13T>G (n.-13T>G) | |
X | g.47566727C>A | CA412813400 | ARAF | c.646C>A (p.Pro216Thr) c.655C>A (p.Pro219Thr) c.661C>A (p.Pro221Thr) c.-12C>A (n.-12C>A) | |
X | g.47566727C>G | CA412813401 | ARAF | c.646C>G (p.Pro216Ala) c.655C>G (p.Pro219Ala) c.661C>G (p.Pro221Ala) c.-12C>G (n.-12C>G) | |
X | g.47566727C>T | CA412813402 | ARAF | c.646C>T (p.Pro216Ser) c.655C>T (p.Pro219Ser) c.661C>T (p.Pro221Ser) c.-12C>T (n.-12C>T) | |
X | g.47566727_47566728delinsTT | CA645603173 | ARAF | c.646_647delinsTT (p.Pro216Phe) c.655_656delinsTT (p.Pro219Phe) c.661_662delinsTT (p.Pro221Phe) c.-12_-11delinsTT (n.-12_-11delinsTT) | COSMIC |
X | g.47566729del | CA2561210337 | ARAF | c.648del (p.Asn217ThrfsTer?) c.657del (p.Asn220ThrfsTer?) c.663del (p.Asn222ThrfsTer?) c.-10del (n.-10del) | |
X | g.47566728C>A | CA412813403 | ARAF | c.647C>A (p.Pro216His) c.656C>A (p.Pro219His) c.662C>A (p.Pro221His) c.-11C>A (n.-11C>A) | |
X | g.47566728C>G | CA412813404 | ARAF | c.647C>G (p.Pro216Arg) c.656C>G (p.Pro219Arg) c.662C>G (p.Pro221Arg) c.-11C>G (n.-11C>G) | |
X | g.47566728C>T | CA412813405 | ARAF | c.647C>T (p.Pro216Leu) c.656C>T (p.Pro219Leu) c.662C>T (p.Pro221Leu) c.-11C>T (n.-11C>T) | COSMIC |
X | g.47566729C>A | CA515989190 | ARAF | c.648C>A (p.Pro216=) c.657C>A (p.Pro219=) c.663C>A (p.Pro221=) c.-10C>A (n.-10C>A) | |
X | g.47566729C>G | CA515989191 | ARAF | c.648C>G (p.Pro216=) c.657C>G (p.Pro219=) c.663C>G (p.Pro221=) c.-10C>G (n.-10C>G) | |
X | g.47566729C>T | CA515989193 | ARAF | c.648C>T (p.Pro216=) c.657C>T (p.Pro219=) c.663C>T (p.Pro221=) c.-10C>T (n.-10C>T) | gnomAD v4 |
X | g.47566730A>C | CA412813406 | ARAF | c.649A>C (p.Asn217His) c.658A>C (p.Asn220His) c.664A>C (p.Asn222His) c.-9A>C (n.-9A>C) | |
X | g.47566730A>G | CA412813407 | ARAF | c.649A>G (p.Asn217Asp) c.658A>G (p.Asn220Asp) c.664A>G (p.Asn222Asp) c.-9A>G (n.-9A>G) | |
X | g.47566730A>T | CA412813408 | ARAF | c.649A>T (p.Asn217Tyr) c.658A>T (p.Asn220Tyr) c.664A>T (p.Asn222Tyr) c.-9A>T (n.-9A>T) | |
X | g.47566731A>C | CA412813409 | ARAF | c.650A>C (p.Asn217Thr) c.659A>C (p.Asn220Thr) c.665A>C (p.Asn222Thr) c.-8A>C (n.-8A>C) | |
X | g.47566731A>G | CA412813410 | ARAF | c.650A>G (p.Asn217Ser) c.659A>G (p.Asn220Ser) c.665A>G (p.Asn222Ser) c.-8A>G (n.-8A>G) | ClinVar gnomAD v4 |
X | g.47566731A>T | CA412813411 | ARAF | c.650A>T (p.Asn217Ile) c.659A>T (p.Asn220Ile) c.665A>T (p.Asn222Ile) c.-8A>T (n.-8A>T) | COSMIC |
X | g.47566732C>A | CA412813413 | ARAF | c.651C>A (p.Asn217Lys) c.660C>A (p.Asn220Lys) c.666C>A (p.Asn222Lys) c.-7C>A (n.-7C>A) | dbSNP COSMIC |
X | g.47566732C= | CA2427968733 | ARAF | c.651C= (p.Asn217=) c.660C= (p.Asn220=) c.666C= (p.Asn222=) c.-7C= (n.-7C=) | |
X | g.47566732C>G | CA412813412 | ARAF | c.651C>G (p.Asn217Lys) c.660C>G (p.Asn220Lys) c.666C>G (p.Asn222Lys) c.-7C>G (n.-7C>G) | |
X | g.47566732C>T | CA515989200 | ARAF | c.651C>T (p.Asn217=) c.660C>T (p.Asn220=) c.666C>T (p.Asn222=) c.-7C>T (n.-7C>T) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47566733G>A | CA412813414 | ARAF | c.652G>A (p.Val218Ile) c.661G>A (p.Val221Ile) c.667G>A (p.Val223Ile) c.-6G>A (n.-6G>A) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47566733G>C | CA412813416 | ARAF | c.652G>C (p.Val218Leu) c.661G>C (p.Val221Leu) c.667G>C (p.Val223Leu) c.-6G>C (n.-6G>C) | dbSNP |
X | g.47566733G= | CA2427968734 | ARAF | c.652G= (p.Val218=) c.661G= (p.Val221=) c.667G= (p.Val223=) c.-6G= (n.-6G=) | |
X | g.47566733G>T | CA412813415 | ARAF | c.652G>T (p.Val218Phe) c.661G>T (p.Val221Phe) c.667G>T (p.Val223Phe) c.-6G>T (n.-6G>T) | |
X | g.47566736_47566744del | CA645603174 | ARAF | c.655_663del (p.His219_Val221del) c.664_672del (p.His222_Val224del) c.670_678del (p.His224_Val226del) c.-3_6del | COSMIC |