Mutation - ICGC |
Project Code | Chromosome | Chromosome Start | Chromosome End | Mutation Type | Mutated from Allele | Mutated to Allele | Consequence Type | AA Mutation | CDS Mutation |
BLCA-CN | 14 | 24682722 | 24682722 | single base substitution | A | C | downstream_gene_variant | | |
BLCA-CN | 14 | 24684759 | 24684759 | single base substitution | T | G | splice_region_variant | | |
BLCA-CN | 14 | 24702539 | 24702539 | single base substitution | G | A | upstream_gene_variant | | |
BLCA-US | 14 | 24687356 | 24687356 | single base substitution | G | A | exon_variant | | |
BLCA-US | 14 | 24687356 | 24687356 | single base substitution | G | A | synonymous_variant | I44I | 132C>T |
BRCA-EU | 14 | 24679428 | 24679428 | single base substitution | C | G | downstream_gene_variant | | |
BRCA-EU | 14 | 24679601 | 24679601 | single base substitution | G | A | downstream_gene_variant | | |
BRCA-EU | 14 | 24682178 | 24682178 | single base substitution | G | C | downstream_gene_variant | | |
BRCA-EU | 14 | 24682619 | 24682619 | single base substitution | C | T | downstream_gene_variant | | |
BRCA-EU | 14 | 24682832 | 24682832 | single base substitution | G | T | downstream_gene_variant | | |
BRCA-EU | 14 | 24683221 | 24683221 | single base substitution | C | T | 3_prime_UTR_variant | | |
BRCA-EU | 14 | 24683221 | 24683221 | single base substitution | C | T | downstream_gene_variant | | |
BRCA-EU | 14 | 24685224 | 24685224 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 14 | 24685651 | 24685651 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 14 | 24685779 | 24685779 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 14 | 24687375 | 24687375 | insertion of <=200bp | - | G | exon_variant | | |
BRCA-EU | 14 | 24687375 | 24687375 | insertion of <=200bp | - | G | frameshift_variant | P38P? | |
BRCA-EU | 14 | 24688405 | 24688405 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 14 | 24692073 | 24692073 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 14 | 24692606 | 24692606 | deletion of <=200bp | A | - | intron_variant | | |
BRCA-EU | 14 | 24693294 | 24693294 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 14 | 24694594 | 24694594 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 14 | 24697325 | 24697325 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 14 | 24697773 | 24697773 | single base substitution | T | C | intron_variant | | |
BRCA-EU | 14 | 24698524 | 24698524 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 14 | 24699190 | 24699190 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 14 | 24700613 | 24700616 | deletion of <=200bp | AAAT | - | intron_variant | | |
BRCA-EU | 14 | 24700871 | 24700871 | deletion of <=200bp | G | - | exon_variant | | |
BRCA-EU | 14 | 24700871 | 24700871 | deletion of <=200bp | G | - | intron_variant | | |
BRCA-EU | 14 | 24701267 | 24701267 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 14 | 24701605 | 24701605 | single base substitution | C | T | upstream_gene_variant | | |
BRCA-EU | 14 | 24701752 | 24701752 | single base substitution | G | C | upstream_gene_variant | | |
BRCA-EU | 14 | 24704359 | 24704359 | single base substitution | G | A | upstream_gene_variant | | |
BRCA-EU | 14 | 24704799 | 24704799 | single base substitution | C | G | upstream_gene_variant | | |
BRCA-EU | 14 | 24704846 | 24704846 | single base substitution | T | G | upstream_gene_variant | | |
BRCA-FR | 14 | 24683221 | 24683221 | single base substitution | C | T | 3_prime_UTR_variant | | |
BRCA-FR | 14 | 24683221 | 24683221 | single base substitution | C | T | downstream_gene_variant | | |
BRCA-FR | 14 | 24683734 | 24683734 | single base substitution | T | G | 3_prime_UTR_variant | | |
BRCA-FR | 14 | 24683734 | 24683734 | single base substitution | T | G | exon_variant | | |
BRCA-FR | 14 | 24683734 | 24683734 | single base substitution | T | G | missense_variant | E111A | 332A>C |
BRCA-FR | 14 | 24685224 | 24685224 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 14 | 24685779 | 24685779 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 14 | 24692073 | 24692073 | single base substitution | C | T | intron_variant | | |
BRCA-FR | 14 | 24694594 | 24694594 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 14 | 24696851 | 24696851 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 14 | 24698524 | 24698524 | single base substitution | C | G | intron_variant | | |
BRCA-FR | 14 | 24701267 | 24701267 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 14 | 24704359 | 24704359 | single base substitution | G | A | upstream_gene_variant | | |
BRCA-UK | 14 | 24680901 | 24680901 | single base substitution | T | C | downstream_gene_variant | | |
BRCA-UK | 14 | 24685135 | 24685135 | single base substitution | G | A | intron_variant | | |
BRCA-UK | 14 | 24692511 | 24692511 | single base substitution | G | A | intron_variant | | |
BRCA-US | 14 | 24680890 | 24680890 | single base substitution | C | G | downstream_gene_variant | | |
BRCA-US | 14 | 24683340 | 24683340 | single base substitution | T | C | 3_prime_UTR_variant | | |
BRCA-US | 14 | 24683340 | 24683340 | single base substitution | T | C | downstream_gene_variant | | |
BRCA-US | 14 | 24683340 | 24683340 | single base substitution | T | C | missense_variant | I158V | 472A>G |
BRCA-US | 14 | 24683764 | 24683764 | single base substitution | A | C | 3_prime_UTR_variant | | |
BRCA-US | 14 | 24683764 | 24683764 | single base substitution | A | C | exon_variant | | |
BRCA-US | 14 | 24683764 | 24683764 | single base substitution | A | C | missense_variant | F101C | 302T>G |
BRCA-US | 14 | 24684867 | 24684867 | single base substitution | C | T | missense_variant | D51N | 151G>A |
BRCA-US | 14 | 24684867 | 24684867 | single base substitution | C | T | splice_region_variant | | |
BRCA-US | 14 | 24687410 | 24687410 | single base substitution | G | C | exon_variant | | |
BRCA-US | 14 | 24687410 | 24687410 | single base substitution | G | C | missense_variant | I26M | 78C>G |
BRCA-US | 14 | 24702445 | 24702445 | single base substitution | C | T | upstream_gene_variant | | |
BTCA-JP | 14 | 24683427 | 24683433 | deletion of <=200bp | TGCCACC | - | downstream_gene_variant | | |
BTCA-JP | 14 | 24683427 | 24683433 | deletion of <=200bp | TGCCACC | - | intron_variant | | |
BTCA-JP | 14 | 24686450 | 24686450 | deletion of <=200bp | A | - | intron_variant | | |
BTCA-JP | 14 | 24686510 | 24686510 | single base substitution | G | T | intron_variant | | |
BTCA-JP | 14 | 24702832 | 24702832 | single base substitution | A | G | upstream_gene_variant | | |
CESC-US | 14 | 24683549 | 24683549 | single base substitution | C | G | 3_prime_UTR_variant | | |
CESC-US | 14 | 24683549 | 24683549 | single base substitution | C | G | downstream_gene_variant | | |
CESC-US | 14 | 24683549 | 24683549 | single base substitution | C | G | missense_variant | E141Q | 421G>C |
CESC-US | 14 | 24684984 | 24684984 | single base substitution | G | A | exon_variant | | |
CESC-US | 14 | 24684984 | 24684984 | single base substitution | G | A | intron_variant | | |
CLLE-ES | 14 | 24698088 | 24698088 | single base substitution | C | G | intron_variant | | |
COAD-US | 14 | 24684996 | 24684996 | single base substitution | A | C | exon_variant | | |
COAD-US | 14 | 24684996 | 24684996 | single base substitution | A | C | intron_variant | | |
COCA-CN | 14 | 24680920 | 24680920 | single base substitution | T | G | downstream_gene_variant | | |
COCA-CN | 14 | 24681054 | 24681054 | single base substitution | T | C | downstream_gene_variant | | |
COCA-CN | 14 | 24685131 | 24685131 | single base substitution | C | A | intron_variant | | |
COCA-CN | 14 | 24686420 | 24686420 | single base substitution | C | A | exon_variant | | |
COCA-CN | 14 | 24686420 | 24686420 | single base substitution | C | A | intron_variant | | |
COCA-CN | 14 | 24687604 | 24687604 | single base substitution | C | G | exon_variant | | |
COCA-CN | 14 | 24687604 | 24687604 | single base substitution | C | G | missense_variant | E18Q | 52G>C |
COCA-CN | 14 | 24702979 | 24702979 | single base substitution | C | G | upstream_gene_variant | | |
COCA-CN | 14 | 24703270 | 24703270 | single base substitution | G | T | upstream_gene_variant | | |
COCA-CN | 14 | 24705034 | 24705034 | single base substitution | T | G | upstream_gene_variant | | |
COCA-CN | 14 | 24706174 | 24706174 | single base substitution | C | A | upstream_gene_variant | | |
COCA-CN | 14 | 24706504 | 24706504 | single base substitution | G | A | upstream_gene_variant | | |
ESAD-UK | 14 | 24682159 | 24682159 | single base substitution | G | T | downstream_gene_variant | | |
ESAD-UK | 14 | 24682301 | 24682301 | single base substitution | C | G | downstream_gene_variant | | |
ESAD-UK | 14 | 24682412 | 24682412 | single base substitution | G | A | downstream_gene_variant | | |
ESAD-UK | 14 | 24688265 | 24688265 | single base substitution | A | T | intron_variant | | |
ESAD-UK | 14 | 24691452 | 24691452 | deletion of <=200bp | A | - | intron_variant | | |
ESAD-UK | 14 | 24691523 | 24691523 | single base substitution | T | C | intron_variant | | |
ESAD-UK | 14 | 24693884 | 24693884 | single base substitution | A | G | intron_variant | | |
ESAD-UK | 14 | 24694131 | 24694131 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 14 | 24694268 | 24694268 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 14 | 24696672 | 24696672 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 14 | 24700504 | 24700504 | single base substitution | T | G | intron_variant | | |
ESAD-UK | 14 | 24700838 | 24700838 | single base substitution | C | T | intron_variant | | |
ESCA-CN | 14 | 24686388 | 24686388 | single base substitution | C | G | intron_variant | | |
ESCA-CN | 14 | 24686388 | 24686388 | single base substitution | C | G | splice_region_variant | | |
GBM-US | 14 | 24683351 | 24683351 | single base substitution | G | A | 3_prime_UTR_variant | | |
GBM-US | 14 | 24683351 | 24683351 | single base substitution | G | A | downstream_gene_variant | | |
GBM-US | 14 | 24683351 | 24683351 | single base substitution | G | A | missense_variant | T154I | 461C>T |
LAML-KR | 14 | 24683125 | 24683125 | single base substitution | A | G | downstream_gene_variant | | |
LAML-KR | 14 | 24695231 | 24695231 | single base substitution | T | G | intron_variant | | |
LAML-KR | 14 | 24705295 | 24705295 | single base substitution | T | C | upstream_gene_variant | | |
LICA-FR | 14 | 24695652 | 24695653 | deletion of <=200bp | AA | - | intron_variant | | |
LINC-JP | 14 | 24678825 | 24678840 | deletion of <=200bp | ATCTGCCCAGTTTTAT | - | downstream_gene_variant | | |
LINC-JP | 14 | 24687512 | 24687512 | single base substitution | A | G | intron_variant | | |
LINC-JP | 14 | 24702766 | 24702766 | insertion of <=200bp | - | A | upstream_gene_variant | | |
LINC-JP | 14 | 24703372 | 24703372 | single base substitution | C | G | upstream_gene_variant | | |
LINC-JP | 14 | 24703773 | 24703773 | single base substitution | A | G | upstream_gene_variant | | |
LINC-JP | 14 | 24704355 | 24704355 | single base substitution | A | C | upstream_gene_variant | | |
LIRI-JP | 14 | 24678904 | 24678904 | single base substitution | A | C | downstream_gene_variant | | |
LIRI-JP | 14 | 24679414 | 24679414 | single base substitution | T | C | downstream_gene_variant | | |
LIRI-JP | 14 | 24681294 | 24681294 | single base substitution | A | G | downstream_gene_variant | | |
LIRI-JP | 14 | 24684073 | 24684073 | single base substitution | C | G | intron_variant | | |
LIRI-JP | 14 | 24685213 | 24685213 | single base substitution | T | C | intron_variant | | |
LIRI-JP | 14 | 24687873 | 24687873 | single base substitution | C | A | intron_variant | | |
LIRI-JP | 14 | 24688990 | 24688990 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 14 | 24692189 | 24692189 | single base substitution | G | T | intron_variant | | |
LIRI-JP | 14 | 24696078 | 24696078 | single base substitution | A | C | intron_variant | | |
LIRI-JP | 14 | 24699008 | 24699008 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 14 | 24699149 | 24699149 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 14 | 24701871 | 24701871 | single base substitution | A | T | upstream_gene_variant | | |
LIRI-JP | 14 | 24702401 | 24702401 | single base substitution | T | G | upstream_gene_variant | | |
LIRI-JP | 14 | 24705931 | 24705931 | single base substitution | A | G | upstream_gene_variant | | |
LIRI-JP | 14 | 24706001 | 24706001 | single base substitution | G | A | upstream_gene_variant | | |
LUSC-KR | 14 | 24678885 | 24678885 | single base substitution | A | C | downstream_gene_variant | | |
LUSC-KR | 14 | 24680005 | 24680005 | single base substitution | C | T | downstream_gene_variant | | |
LUSC-KR | 14 | 24687771 | 24687771 | single base substitution | G | A | intron_variant | | |
LUSC-KR | 14 | 24688023 | 24688023 | single base substitution | G | A | intron_variant | | |
LUSC-KR | 14 | 24689246 | 24689246 | single base substitution | G | A | intron_variant | | |
LUSC-KR | 14 | 24692945 | 24692945 | single base substitution | A | T | intron_variant | | |
LUSC-KR | 14 | 24697059 | 24697059 | single base substitution | G | T | intron_variant | | |
LUSC-KR | 14 | 24700194 | 24700194 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 14 | 24700712 | 24700712 | single base substitution | T | G | intron_variant | | |
LUSC-US | 14 | 24684816 | 24684816 | single base substitution | C | A | 3_prime_UTR_variant | | |
LUSC-US | 14 | 24684816 | 24684816 | single base substitution | C | A | exon_variant | | |
LUSC-US | 14 | 24684816 | 24684816 | single base substitution | C | A | missense_variant | V68L | 202G>T |
MALY-DE | 14 | 24681701 | 24681701 | single base substitution | T | A | downstream_gene_variant | | |
MALY-DE | 14 | 24683695 | 24683695 | single base substitution | T | C | splice_region_variant | | |
MALY-DE | 14 | 24684755 | 24684755 | single base substitution | T | C | splice_region_variant | | |
MALY-DE | 14 | 24692872 | 24692872 | single base substitution | A | C | intron_variant | | |
MALY-DE | 14 | 24696288 | 24696288 | single base substitution | A | G | intron_variant | | |
MALY-DE | 14 | 24696311 | 24696311 | single base substitution | T | G | intron_variant | | |
MELA-AU | 14 | 24679260 | 24679260 | single base substitution | C | A | downstream_gene_variant | | |
MELA-AU | 14 | 24679720 | 24679720 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 14 | 24680174 | 24680174 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 14 | 24680316 | 24680316 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 14 | 24680824 | 24680824 | single base substitution | C | T | downstream_gene_variant | | |
MELA-AU | 14 | 24681051 | 24681051 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 14 | 24682560 | 24682560 | single base substitution | C | T | downstream_gene_variant | | |
MELA-AU | 14 | 24682731 | 24682731 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 14 | 24683082 | 24683082 | single base substitution | C | T | downstream_gene_variant | | |
MELA-AU | 14 | 24684988 | 24684989 | multiple base substitution (>=2bp and <=200bp) | GG | TA | exon_variant | | |
MELA-AU | 14 | 24684988 | 24684989 | multiple base substitution (>=2bp and <=200bp) | GG | TA | intron_variant | | |
MELA-AU | 14 | 24685776 | 24685776 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24686176 | 24686176 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24686435 | 24686435 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24686435 | 24686435 | single base substitution | G | A | splice_region_variant | | |
MELA-AU | 14 | 24687380 | 24687380 | single base substitution | G | A | exon_variant | | |
MELA-AU | 14 | 24687380 | 24687380 | single base substitution | G | A | synonymous_variant | I36I | 108C>T |
MELA-AU | 14 | 24687477 | 24687477 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24687600 | 24687601 | multiple base substitution (>=2bp and <=200bp) | GG | AA | exon_variant | | |
MELA-AU | 14 | 24687600 | 24687601 | multiple base substitution (>=2bp and <=200bp) | GG | AA | missense_variant | P19F | 55CC>TT |
MELA-AU | 14 | 24687975 | 24687976 | multiple base substitution (>=2bp and <=200bp) | GG | AA | intron_variant | | |
MELA-AU | 14 | 24688231 | 24688231 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24688374 | 24688374 | single base substitution | A | G | intron_variant | | |
MELA-AU | 14 | 24688400 | 24688400 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24689597 | 24689597 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24690014 | 24690014 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24690128 | 24690128 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24690311 | 24690311 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24690628 | 24690628 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24690835 | 24690835 | single base substitution | C | T | intron_variant | | |
MELA-AU | 14 | 24690965 | 24690965 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24691115 | 24691115 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24692476 | 24692476 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24692588 | 24692588 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24692590 | 24692590 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24692746 | 24692746 | single base substitution | T | C | intron_variant | | |
MELA-AU | 14 | 24692984 | 24692984 | single base substitution | C | T | intron_variant | | |
MELA-AU | 14 | 24693182 | 24693182 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24693761 | 24693761 | single base substitution | C | T | intron_variant | | |
MELA-AU | 14 | 24694714 | 24694714 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24695161 | 24695161 | single base substitution | C | A | intron_variant | | |
MELA-AU | 14 | 24695163 | 24695163 | single base substitution | T | A | intron_variant | | |
MELA-AU | 14 | 24696116 | 24696116 | single base substitution | A | C | intron_variant | | |
MELA-AU | 14 | 24696156 | 24696156 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24696529 | 24696529 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24696630 | 24696630 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24697993 | 24697993 | single base substitution | T | C | intron_variant | | |
MELA-AU | 14 | 24698860 | 24698860 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24698871 | 24698871 | single base substitution | A | G | intron_variant | | |
MELA-AU | 14 | 24699986 | 24699986 | single base substitution | G | A | intron_variant | | |
MELA-AU | 14 | 24701578 | 24701578 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 14 | 24704419 | 24704419 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 14 | 24706169 | 24706170 | multiple base substitution (>=2bp and <=200bp) | CC | TT | upstream_gene_variant | | |
OV-AU | 14 | 24680174 | 24680174 | single base substitution | G | C | downstream_gene_variant | | |
OV-AU | 14 | 24680366 | 24680366 | single base substitution | G | C | downstream_gene_variant | | |
OV-AU | 14 | 24681576 | 24681576 | single base substitution | C | G | downstream_gene_variant | | |
OV-AU | 14 | 24684921 | 24684921 | single base substitution | G | T | intron_variant | | |
OV-AU | 14 | 24685537 | 24685537 | single base substitution | T | C | intron_variant | | |
OV-AU | 14 | 24694264 | 24694264 | single base substitution | C | G | intron_variant | | |
OV-AU | 14 | 24695264 | 24695264 | single base substitution | A | C | intron_variant | | |
OV-AU | 14 | 24703022 | 24703022 | single base substitution | T | G | upstream_gene_variant | | |
PACA-AU | 14 | 24678724 | 24678726 | deletion of <=200bp | CCC | - | downstream_gene_variant | | |
PACA-AU | 14 | 24681817 | 24681817 | single base substitution | T | C | downstream_gene_variant | | |
PACA-AU | 14 | 24684475 | 24684475 | single base substitution | A | G | intron_variant | | |
PACA-AU | 14 | 24694227 | 24694227 | single base substitution | T | C | intron_variant | | |
PACA-AU | 14 | 24696698 | 24696698 | single base substitution | G | A | intron_variant | | |
PACA-AU | 14 | 24699184 | 24699184 | single base substitution | G | A | intron_variant | | |
PACA-AU | 14 | 24699522 | 24699522 | single base substitution | C | T | intron_variant | | |
PACA-CA | 14 | 24678913 | 24678913 | single base substitution | T | C | downstream_gene_variant | | |
PACA-CA | 14 | 24688410 | 24688410 | single base substitution | G | A | intron_variant | | |
PACA-CA | 14 | 24692749 | 24692749 | single base substitution | A | T | intron_variant | | |
PACA-CA | 14 | 24704861 | 24704861 | single base substitution | C | G | upstream_gene_variant | | |
PACA-CA | 14 | 24704864 | 24704864 | single base substitution | A | C | upstream_gene_variant | | |
PACA-CA | 14 | 24704937 | 24704937 | single base substitution | C | G | upstream_gene_variant | | |
PACA-CA | 14 | 24705553 | 24705553 | single base substitution | T | C | upstream_gene_variant | | |
PAEN-AU | 14 | 24695637 | 24695637 | single base substitution | G | C | intron_variant | | |
PBCA-DE | 14 | 24687403 | 24687403 | single base substitution | G | A | exon_variant | | |
PBCA-DE | 14 | 24687403 | 24687403 | single base substitution | G | A | missense_variant | R29C | 85C>T |
PBCA-DE | 14 | 24696711 | 24696711 | single base substitution | G | C | intron_variant | | |
PRAD-CA | 14 | 24693643 | 24693643 | single base substitution | C | G | intron_variant | | |
PRAD-UK | 14 | 24680412 | 24680412 | deletion of <=200bp | A | - | downstream_gene_variant | | |
PRAD-UK | 14 | 24686652 | 24686652 | single base substitution | C | T | intron_variant | | |
PRAD-US | 14 | 24682652 | 24682652 | single base substitution | C | G | downstream_gene_variant | | |
PRAD-US | 14 | 24702732 | 24702732 | single base substitution | C | A | upstream_gene_variant | | |
READ-US | 14 | 24679894 | 24679894 | single base substitution | G | T | downstream_gene_variant | | |
READ-US | 14 | 24680711 | 24680711 | single base substitution | C | T | downstream_gene_variant | | |
READ-US | 14 | 24683287 | 24683287 | single base substitution | C | T | 3_prime_UTR_variant | | |
READ-US | 14 | 24683287 | 24683287 | single base substitution | C | T | downstream_gene_variant | | |
READ-US | 14 | 24683741 | 24683741 | single base substitution | G | T | 3_prime_UTR_variant | | |
READ-US | 14 | 24683741 | 24683741 | single base substitution | G | T | exon_variant | | |
READ-US | 14 | 24683741 | 24683741 | single base substitution | G | T | missense_variant | H109N | 325C>A |
READ-US | 14 | 24706350 | 24706350 | single base substitution | T | G | upstream_gene_variant | | |
RECA-EU | 14 | 24682705 | 24682705 | single base substitution | T | A | downstream_gene_variant | | |
RECA-EU | 14 | 24685655 | 24685655 | single base substitution | G | A | intron_variant | | |
RECA-EU | 14 | 24698109 | 24698109 | single base substitution | A | T | intron_variant | | |
SKCA-BR | 14 | 24681486 | 24681486 | single base substitution | A | C | downstream_gene_variant | | |
SKCA-BR | 14 | 24681755 | 24681755 | single base substitution | A | C | downstream_gene_variant | | |
SKCA-BR | 14 | 24682636 | 24682636 | single base substitution | G | C | downstream_gene_variant | | |
SKCA-BR | 14 | 24684638 | 24684638 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 14 | 24686436 | 24686436 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 14 | 24686436 | 24686436 | single base substitution | G | A | splice_region_variant | | |
SKCA-BR | 14 | 24687457 | 24687457 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 14 | 24692932 | 24692932 | insertion of <=200bp | - | GA | intron_variant | | |
SKCA-BR | 14 | 24693513 | 24693513 | single base substitution | A | C | intron_variant | | |
SKCA-BR | 14 | 24694377 | 24694377 | insertion of <=200bp | - | CA | intron_variant | | |
SKCA-BR | 14 | 24702453 | 24702453 | single base substitution | A | G | upstream_gene_variant | | |
SKCM-US | 14 | 24680673 | 24680673 | single base substitution | G | A | downstream_gene_variant | | |
SKCM-US | 14 | 24682669 | 24682669 | single base substitution | C | A | downstream_gene_variant | | |
SKCM-US | 14 | 24682688 | 24682688 | single base substitution | G | A | downstream_gene_variant | | |
SKCM-US | 14 | 24684863 | 24684863 | single base substitution | C | T | 3_prime_UTR_variant | | |
SKCM-US | 14 | 24684863 | 24684863 | single base substitution | C | T | exon_variant | | |
SKCM-US | 14 | 24684863 | 24684863 | single base substitution | C | T | missense_variant | G52E | 155G>A |
SKCM-US | 14 | 24701578 | 24701578 | single base substitution | C | T | upstream_gene_variant | | |
SKCM-US | 14 | 24706339 | 24706339 | single base substitution | C | T | upstream_gene_variant | | |
STAD-US | 14 | 24679618 | 24679618 | single base substitution | G | A | downstream_gene_variant | | |
STAD-US | 14 | 24705334 | 24705334 | single base substitution | G | A | upstream_gene_variant | | |
UCEC-US | 14 | 24680896 | 24680896 | single base substitution | C | A | downstream_gene_variant | | |
UCEC-US | 14 | 24683240 | 24683240 | single base substitution | A | C | 3_prime_UTR_variant | | |
UCEC-US | 14 | 24683240 | 24683240 | single base substitution | A | C | downstream_gene_variant | | |
UCEC-US | 14 | 24683257 | 24683257 | single base substitution | G | A | 3_prime_UTR_variant | | |
UCEC-US | 14 | 24683257 | 24683257 | single base substitution | G | A | downstream_gene_variant | | |
UCEC-US | 14 | 24683309 | 24683309 | single base substitution | C | T | 3_prime_UTR_variant | | |
UCEC-US | 14 | 24683309 | 24683309 | single base substitution | C | T | downstream_gene_variant | | |
UCEC-US | 14 | 24683309 | 24683309 | single base substitution | C | T | missense_variant | S168N | 503G>A |
UCEC-US | 14 | 24686360 | 24686360 | single base substitution | C | G | intron_variant | | |
UCEC-US | 14 | 24702774 | 24702774 | single base substitution | C | T | upstream_gene_variant | | |
UCEC-US | 14 | 24704989 | 24704989 | single base substitution | G | C | upstream_gene_variant | | |
UCEC-US | 14 | 24706542 | 24706542 | single base substitution | A | T | upstream_gene_variant | | |