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 | 16 | 4407981 | 4407981 | single base substitution | C | T | 3_prime_UTR_variant | | |
BLCA-CN | 16 | 4407981 | 4407981 | single base substitution | C | T | exon_variant | | |
BLCA-CN | 16 | 4407981 | 4407981 | single base substitution | C | T | missense_variant | D861N | 2581G>A |
BLCA-CN | 16 | 4411167 | 4411167 | single base substitution | G | A | 3_prime_UTR_variant | | |
BLCA-CN | 16 | 4411167 | 4411167 | single base substitution | G | A | synonymous_variant | L590L | 1770C>T |
BLCA-CN | 16 | 4411167 | 4411167 | single base substitution | G | A | upstream_gene_variant | | |
BLCA-CN | 16 | 4411206 | 4411206 | single base substitution | C | G | 3_prime_UTR_variant | | |
BLCA-CN | 16 | 4411206 | 4411206 | single base substitution | C | G | missense_variant | E577D | 1731G>C |
BLCA-CN | 16 | 4411206 | 4411206 | single base substitution | C | G | upstream_gene_variant | | |
BLCA-US | 16 | 4390379 | 4390379 | single base substitution | C | T | 3_prime_UTR_variant | | |
BLCA-US | 16 | 4390379 | 4390379 | single base substitution | C | T | downstream_gene_variant | | |
BLCA-US | 16 | 4390379 | 4390379 | single base substitution | C | T | missense_variant | E1030K | 3088G>A |
BLCA-US | 16 | 4411441 | 4411441 | single base substitution | C | T | 3_prime_UTR_variant | | |
BLCA-US | 16 | 4411441 | 4411441 | single base substitution | C | T | synonymous_variant | T536T | 1608G>A |
BLCA-US | 16 | 4411441 | 4411441 | single base substitution | C | T | upstream_gene_variant | | |
BLCA-US | 16 | 4412079 | 4412079 | single base substitution | G | A | exon_variant | | |
BLCA-US | 16 | 4412079 | 4412079 | single base substitution | G | A | synonymous_variant | L495L | 1485C>T |
BLCA-US | 16 | 4412079 | 4412079 | single base substitution | G | A | upstream_gene_variant | | |
BLCA-US | 16 | 4431070 | 4431070 | single base substitution | C | T | intron_variant | | |
BLCA-US | 16 | 4466517 | 4466517 | single base substitution | C | T | exon_variant | | |
BLCA-US | 16 | 4466517 | 4466517 | single base substitution | C | T | start_lost | M1I | 3G>A |
BOCA-FR | 16 | 4406754 | 4406754 | single base substitution | A | G | intron_variant | | |
BRCA-EU | 16 | 4386157 | 4386157 | deletion of <=200bp | T | - | downstream_gene_variant | | |
BRCA-EU | 16 | 4386264 | 4386264 | single base substitution | C | A | downstream_gene_variant | | |
BRCA-EU | 16 | 4387070 | 4387070 | single base substitution | C | T | downstream_gene_variant | | |
BRCA-EU | 16 | 4389122 | 4389122 | single base substitution | C | G | downstream_gene_variant | | |
BRCA-EU | 16 | 4389199 | 4389199 | single base substitution | C | G | downstream_gene_variant | | |
BRCA-EU | 16 | 4389231 | 4389231 | single base substitution | C | T | downstream_gene_variant | | |
BRCA-EU | 16 | 4389254 | 4389254 | single base substitution | G | A | downstream_gene_variant | | |
BRCA-EU | 16 | 4389737 | 4389737 | single base substitution | A | T | downstream_gene_variant | | |
BRCA-EU | 16 | 4390987 | 4390987 | single base substitution | C | T | splice_acceptor_variant | | |
BRCA-EU | 16 | 4392168 | 4392168 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4392655 | 4392655 | single base substitution | T | A | intron_variant | | |
BRCA-EU | 16 | 4392656 | 4392656 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4393860 | 4393860 | single base substitution | G | T | intron_variant | | |
BRCA-EU | 16 | 4395254 | 4395254 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4396947 | 4396947 | single base substitution | T | A | intron_variant | | |
BRCA-EU | 16 | 4397857 | 4397857 | single base substitution | A | G | intron_variant | | |
BRCA-EU | 16 | 4398296 | 4398296 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4398367 | 4398367 | deletion of <=200bp | C | - | intron_variant | | |
BRCA-EU | 16 | 4398617 | 4398617 | single base substitution | G | T | intron_variant | | |
BRCA-EU | 16 | 4399692 | 4399692 | single base substitution | T | G | intron_variant | | |
BRCA-EU | 16 | 4400524 | 4400524 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4400588 | 4400588 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4400765 | 4400765 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4404290 | 4404290 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4404875 | 4404875 | single base substitution | G | T | intron_variant | | |
BRCA-EU | 16 | 4408197 | 4408197 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4408199 | 4408199 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4409063 | 4409063 | single base substitution | T | A | intron_variant | | |
BRCA-EU | 16 | 4410989 | 4410989 | single base substitution | A | T | 3_prime_UTR_variant | | |
BRCA-EU | 16 | 4410989 | 4410989 | single base substitution | A | T | synonymous_variant | L624L | 1872T>A |
BRCA-EU | 16 | 4410989 | 4410989 | single base substitution | A | T | upstream_gene_variant | | |
BRCA-EU | 16 | 4411127 | 4411127 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4411127 | 4411127 | single base substitution | C | A | upstream_gene_variant | | |
BRCA-EU | 16 | 4413268 | 4413268 | deletion of <=200bp | A | - | intron_variant | | |
BRCA-EU | 16 | 4413268 | 4413268 | deletion of <=200bp | A | - | upstream_gene_variant | | |
BRCA-EU | 16 | 4413913 | 4413913 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4413913 | 4413913 | single base substitution | G | A | upstream_gene_variant | | |
BRCA-EU | 16 | 4414007 | 4414007 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4414007 | 4414007 | single base substitution | C | T | upstream_gene_variant | | |
BRCA-EU | 16 | 4414634 | 4414634 | single base substitution | G | A | exon_variant | | |
BRCA-EU | 16 | 4414634 | 4414634 | single base substitution | G | A | synonymous_variant | T367T | 1101C>T |
BRCA-EU | 16 | 4414759 | 4414759 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4414925 | 4414925 | single base substitution | T | A | splice_region_variant | | |
BRCA-EU | 16 | 4415226 | 4415226 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4417992 | 4417992 | single base substitution | T | C | intron_variant | | |
BRCA-EU | 16 | 4419072 | 4419072 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4419242 | 4419242 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4423427 | 4423427 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4423637 | 4423637 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4425583 | 4425583 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4425722 | 4425722 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4430239 | 4430239 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4432023 | 4432023 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4432267 | 4432267 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4432425 | 4432425 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4432513 | 4432513 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4434403 | 4434403 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4435702 | 4435702 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4437653 | 4437664 | deletion of <=200bp | GAAAAATGAAGC | - | intron_variant | | |
BRCA-EU | 16 | 4437697 | 4437697 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4438483 | 4438483 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4439528 | 4439528 | deletion of <=200bp | C | - | intron_variant | | |
BRCA-EU | 16 | 4439881 | 4439881 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4440058 | 4440058 | deletion of <=200bp | G | - | intron_variant | | |
BRCA-EU | 16 | 4440843 | 4440843 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4441785 | 4441785 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4441839 | 4441839 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4442708 | 4442708 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4444076 | 4444079 | deletion of <=200bp | TGGG | - | intron_variant | | |
BRCA-EU | 16 | 4444174 | 4444174 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4444979 | 4444979 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4446265 | 4446265 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4446517 | 4446517 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4447592 | 4447592 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4450075 | 4450075 | single base substitution | T | A | intron_variant | | |
BRCA-EU | 16 | 4451314 | 4451314 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4452421 | 4452421 | deletion of <=200bp | T | - | intron_variant | | |
BRCA-EU | 16 | 4452474 | 4452474 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4452840 | 4452840 | single base substitution | G | T | intron_variant | | |
BRCA-EU | 16 | 4454978 | 4454978 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4455458 | 4455458 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4455865 | 4455865 | single base substitution | C | G | intron_variant | | |
BRCA-EU | 16 | 4456218 | 4456218 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4460699 | 4460699 | single base substitution | T | C | intron_variant | | |
BRCA-EU | 16 | 4460700 | 4460700 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4460749 | 4460749 | single base substitution | G | C | intron_variant | | |
BRCA-EU | 16 | 4461559 | 4461559 | single base substitution | T | A | intron_variant | | |
BRCA-EU | 16 | 4461560 | 4461560 | single base substitution | A | T | intron_variant | | |
BRCA-EU | 16 | 4461761 | 4461761 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4462546 | 4462546 | single base substitution | C | A | intron_variant | | |
BRCA-EU | 16 | 4462570 | 4462570 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4463024 | 4463024 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4463542 | 4463542 | insertion of <=200bp | - | T | intron_variant | | |
BRCA-EU | 16 | 4464004 | 4464004 | single base substitution | A | G | intron_variant | | |
BRCA-EU | 16 | 4465488 | 4465488 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4467305 | 4467316 | deletion of <=200bp | AATAATAATAAT | - | intron_variant | | |
BRCA-EU | 16 | 4467305 | 4467316 | deletion of <=200bp | AATAATAATAAT | - | upstream_gene_variant | | |
BRCA-EU | 16 | 4468298 | 4468298 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4468298 | 4468298 | single base substitution | G | A | upstream_gene_variant | | |
BRCA-EU | 16 | 4468605 | 4468605 | single base substitution | G | A | intron_variant | | |
BRCA-EU | 16 | 4468605 | 4468605 | single base substitution | G | A | upstream_gene_variant | | |
BRCA-EU | 16 | 4469966 | 4469966 | single base substitution | C | T | intron_variant | | |
BRCA-EU | 16 | 4469966 | 4469966 | single base substitution | C | T | upstream_gene_variant | | |
BRCA-EU | 16 | 4471265 | 4471265 | single base substitution | C | T | upstream_gene_variant | | |
BRCA-EU | 16 | 4472097 | 4472097 | single base substitution | T | A | upstream_gene_variant | | |
BRCA-EU | 16 | 4474118 | 4474118 | single base substitution | C | T | upstream_gene_variant | | |
BRCA-EU | 16 | 4474171 | 4474171 | single base substitution | G | C | upstream_gene_variant | | |
BRCA-EU | 16 | 4475109 | 4475109 | single base substitution | G | C | upstream_gene_variant | | |
BRCA-FR | 16 | 4390987 | 4390987 | single base substitution | C | T | splice_acceptor_variant | | |
BRCA-FR | 16 | 4398296 | 4398296 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 16 | 4398617 | 4398617 | single base substitution | G | T | intron_variant | | |
BRCA-FR | 16 | 4404290 | 4404290 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 16 | 4415226 | 4415226 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 16 | 4435676 | 4435676 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 16 | 4438928 | 4438928 | single base substitution | C | A | intron_variant | | |
BRCA-FR | 16 | 4461583 | 4461583 | single base substitution | C | T | intron_variant | | |
BRCA-FR | 16 | 4463024 | 4463024 | single base substitution | G | A | intron_variant | | |
BRCA-FR | 16 | 4463557 | 4463557 | single base substitution | G | C | intron_variant | | |
BRCA-FR | 16 | 4475109 | 4475109 | single base substitution | G | C | upstream_gene_variant | | |
BRCA-UK | 16 | 4393369 | 4393369 | single base substitution | G | C | intron_variant | | |
BRCA-UK | 16 | 4405797 | 4405797 | single base substitution | G | A | intron_variant | | |
BRCA-UK | 16 | 4450075 | 4450075 | single base substitution | T | A | intron_variant | | |
BRCA-US | 16 | 4390310 | 4390310 | single base substitution | A | G | 3_prime_UTR_variant | | |
BRCA-US | 16 | 4390310 | 4390310 | single base substitution | A | G | downstream_gene_variant | | |
BRCA-US | 16 | 4390379 | 4390379 | single base substitution | C | A | 3_prime_UTR_variant | | |
BRCA-US | 16 | 4390379 | 4390379 | single base substitution | C | A | downstream_gene_variant | | |
BRCA-US | 16 | 4390379 | 4390379 | single base substitution | C | A | stop_gained | E1030* | 3088G>T |
BRCA-US | 16 | 4408084 | 4408084 | single base substitution | G | A | 3_prime_UTR_variant | | |
BRCA-US | 16 | 4408084 | 4408084 | single base substitution | G | A | exon_variant | | |
BRCA-US | 16 | 4408084 | 4408084 | single base substitution | G | A | synonymous_variant | D826D | 2478C>T |
BRCA-US | 16 | 4412030 | 4412030 | single base substitution | C | T | exon_variant | | |
BRCA-US | 16 | 4412030 | 4412030 | single base substitution | C | T | missense_variant | A512T | 1534G>A |
BRCA-US | 16 | 4412030 | 4412030 | single base substitution | C | T | upstream_gene_variant | | |
BRCA-US | 16 | 4412087 | 4412087 | insertion of <=200bp | - | C | exon_variant | | |
BRCA-US | 16 | 4412087 | 4412087 | insertion of <=200bp | - | C | frameshift_variant | L493R? | |
BRCA-US | 16 | 4412087 | 4412087 | insertion of <=200bp | - | C | upstream_gene_variant | | |
BRCA-US | 16 | 4412094 | 4412094 | single base substitution | G | C | exon_variant | | |
BRCA-US | 16 | 4412094 | 4412094 | single base substitution | G | C | synonymous_variant | L490L | 1470C>G |
BRCA-US | 16 | 4412094 | 4412094 | single base substitution | G | C | upstream_gene_variant | | |
BRCA-US | 16 | 4415517 | 4415517 | single base substitution | G | T | exon_variant | | |
BRCA-US | 16 | 4415517 | 4415517 | single base substitution | G | T | missense_variant | S272Y | 815C>A |
BRCA-US | 16 | 4430999 | 4430999 | single base substitution | C | T | intron_variant | | |
BRCA-US | 16 | 4431228 | 4431228 | single base substitution | A | G | intron_variant | | |
BRCA-US | 16 | 4458194 | 4458194 | single base substitution | C | A | exon_variant | | |
BRCA-US | 16 | 4458194 | 4458194 | single base substitution | C | A | synonymous_variant | S97S | 291G>T |
BRCA-US | 16 | 4462374 | 4462374 | single base substitution | T | G | exon_variant | | |
BRCA-US | 16 | 4462374 | 4462374 | single base substitution | T | G | missense_variant | H72P | 215A>C |
BTCA-JP | 16 | 4387168 | 4387168 | single base substitution | C | G | downstream_gene_variant | | |
BTCA-JP | 16 | 4393254 | 4393254 | single base substitution | C | A | 3_prime_UTR_variant | | |
BTCA-JP | 16 | 4393254 | 4393254 | single base substitution | C | A | intron_variant | | |
BTCA-JP | 16 | 4393254 | 4393254 | single base substitution | C | A | missense_variant | Q937H | 2811G>T |
BTCA-JP | 16 | 4410862 | 4410862 | single base substitution | A | T | intron_variant | | |
BTCA-JP | 16 | 4410862 | 4410862 | single base substitution | A | T | upstream_gene_variant | | |
BTCA-JP | 16 | 4410903 | 4410903 | single base substitution | G | A | intron_variant | | |
BTCA-JP | 16 | 4410903 | 4410903 | single base substitution | G | A | upstream_gene_variant | | |
BTCA-JP | 16 | 4410909 | 4410909 | single base substitution | C | G | intron_variant | | |
BTCA-JP | 16 | 4410909 | 4410909 | single base substitution | C | G | upstream_gene_variant | | |
BTCA-JP | 16 | 4415023 | 4415023 | single base substitution | C | G | exon_variant | | |
BTCA-JP | 16 | 4415023 | 4415023 | single base substitution | C | G | missense_variant | Q293H | 879G>C |
BTCA-JP | 16 | 4431535 | 4431535 | single base substitution | C | T | intron_variant | | |
BTCA-JP | 16 | 4432644 | 4432644 | single base substitution | C | T | intron_variant | | |
CESC-US | 16 | 4385353 | 4385353 | single base substitution | C | T | downstream_gene_variant | | |
CESC-US | 16 | 4386876 | 4386876 | single base substitution | C | T | downstream_gene_variant | | |
CESC-US | 16 | 4386904 | 4386904 | single base substitution | C | T | downstream_gene_variant | | |
CESC-US | 16 | 4387454 | 4387454 | single base substitution | G | A | downstream_gene_variant | | |
CESC-US | 16 | 4387480 | 4387480 | single base substitution | C | T | downstream_gene_variant | | |
CESC-US | 16 | 4387793 | 4387793 | single base substitution | G | C | downstream_gene_variant | | |
CESC-US | 16 | 4409516 | 4409516 | single base substitution | C | G | 3_prime_UTR_variant | | |
CESC-US | 16 | 4409516 | 4409516 | single base substitution | C | G | missense_variant | D739H | 2215G>C |
CESC-US | 16 | 4409516 | 4409516 | single base substitution | C | G | upstream_gene_variant | | |
CESC-US | 16 | 4410478 | 4410478 | single base substitution | G | A | 3_prime_UTR_variant | | |
CESC-US | 16 | 4410478 | 4410478 | single base substitution | G | A | synonymous_variant | V663V | 1989C>T |
CESC-US | 16 | 4410478 | 4410478 | single base substitution | G | A | upstream_gene_variant | | |
CESC-US | 16 | 4412623 | 4412623 | single base substitution | C | G | exon_variant | | |
CESC-US | 16 | 4412623 | 4412623 | single base substitution | C | G | missense_variant | Q464H | 1392G>C |
CESC-US | 16 | 4412623 | 4412623 | single base substitution | C | G | upstream_gene_variant | | |
CESC-US | 16 | 4415047 | 4415047 | single base substitution | C | G | exon_variant | | |
CESC-US | 16 | 4415047 | 4415047 | single base substitution | C | G | synonymous_variant | L285L | 855G>C |
CESC-US | 16 | 4431256 | 4431256 | single base substitution | C | T | intron_variant | | |
CESC-US | 16 | 4432189 | 4432189 | single base substitution | G | A | intron_variant | | |
CLLE-ES | 16 | 4402809 | 4402809 | single base substitution | A | T | intron_variant | | |
CLLE-ES | 16 | 4460495 | 4460495 | single base substitution | G | C | intron_variant | | |
CLLE-ES | 16 | 4464712 | 4464712 | single base substitution | T | C | intron_variant | | |
COAD-US | 16 | 4385387 | 4385387 | single base substitution | G | A | downstream_gene_variant | | |
COAD-US | 16 | 4386961 | 4386961 | single base substitution | G | A | downstream_gene_variant | | |
COAD-US | 16 | 4386971 | 4386971 | single base substitution | G | A | downstream_gene_variant | | |
COAD-US | 16 | 4387133 | 4387133 | deletion of <=200bp | G | - | downstream_gene_variant | | |
COAD-US | 16 | 4387300 | 4387300 | single base substitution | G | A | downstream_gene_variant | | |
COAD-US | 16 | 4387495 | 4387495 | single base substitution | G | A | downstream_gene_variant | | |
COAD-US | 16 | 4390345 | 4390346 | deletion of <=200bp | TC | - | 3_prime_UTR_variant | | |
COAD-US | 16 | 4390345 | 4390346 | deletion of <=200bp | TC | - | downstream_gene_variant | | |
COAD-US | 16 | 4390345 | 4390346 | deletion of <=200bp | TC | - | frameshift_variant | E1041 | |
COAD-US | 16 | 4391481 | 4391481 | single base substitution | C | T | 3_prime_UTR_variant | | |
COAD-US | 16 | 4391481 | 4391481 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4391481 | 4391481 | single base substitution | C | T | missense_variant | R961Q | 2882G>A |
COAD-US | 16 | 4408020 | 4408020 | single base substitution | C | T | 3_prime_UTR_variant | | |
COAD-US | 16 | 4408020 | 4408020 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4408020 | 4408020 | single base substitution | C | T | missense_variant | A848T | 2542G>A |
COAD-US | 16 | 4408375 | 4408375 | single base substitution | C | T | 3_prime_UTR_variant | | |
COAD-US | 16 | 4408375 | 4408375 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4408375 | 4408375 | single base substitution | C | T | missense_variant | R817Q | 2450G>A |
COAD-US | 16 | 4412007 | 4412007 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4412007 | 4412007 | single base substitution | C | T | synonymous_variant | G519G | 1557G>A |
COAD-US | 16 | 4412007 | 4412007 | single base substitution | C | T | upstream_gene_variant | | |
COAD-US | 16 | 4412704 | 4412704 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4412704 | 4412704 | single base substitution | C | T | synonymous_variant | S437S | 1311G>A |
COAD-US | 16 | 4412704 | 4412704 | single base substitution | C | T | upstream_gene_variant | | |
COAD-US | 16 | 4414673 | 4414673 | single base substitution | C | A | exon_variant | | |
COAD-US | 16 | 4414673 | 4414673 | single base substitution | C | A | missense_variant | E354D | 1062G>T |
COAD-US | 16 | 4414805 | 4414805 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4414805 | 4414805 | single base substitution | C | T | missense_variant | V339M | 1015G>A |
COAD-US | 16 | 4431373 | 4431373 | single base substitution | G | C | intron_variant | | |
COAD-US | 16 | 4431525 | 4431525 | single base substitution | G | A | intron_variant | | |
COAD-US | 16 | 4431830 | 4431830 | single base substitution | G | A | intron_variant | | |
COAD-US | 16 | 4432072 | 4432072 | single base substitution | G | A | intron_variant | | |
COAD-US | 16 | 4432496 | 4432496 | deletion of <=200bp | C | - | intron_variant | | |
COAD-US | 16 | 4438579 | 4438579 | single base substitution | G | T | exon_variant | | |
COAD-US | 16 | 4438579 | 4438579 | single base substitution | G | T | synonymous_variant | T223T | 669C>A |
COAD-US | 16 | 4455501 | 4455501 | single base substitution | C | T | exon_variant | | |
COAD-US | 16 | 4455501 | 4455501 | single base substitution | C | T | synonymous_variant | T185T | 555G>A |
COAD-US | 16 | 4457527 | 4457527 | single base substitution | G | A | exon_variant | | |
COAD-US | 16 | 4457527 | 4457527 | single base substitution | G | A | synonymous_variant | D154D | 462C>T |
COCA-CN | 16 | 4386945 | 4386945 | single base substitution | G | A | downstream_gene_variant | | |
COCA-CN | 16 | 4386961 | 4386961 | single base substitution | G | A | downstream_gene_variant | | |
COCA-CN | 16 | 4390950 | 4390950 | single base substitution | C | T | 3_prime_UTR_variant | | |
COCA-CN | 16 | 4390950 | 4390950 | single base substitution | C | T | exon_variant | | |
COCA-CN | 16 | 4390950 | 4390950 | single base substitution | C | T | missense_variant | V1011M | 3031G>A |
COCA-CN | 16 | 4393260 | 4393260 | single base substitution | G | A | 3_prime_UTR_variant | | |
COCA-CN | 16 | 4393260 | 4393260 | single base substitution | G | A | intron_variant | | |
COCA-CN | 16 | 4393260 | 4393260 | single base substitution | G | A | synonymous_variant | G935G | 2805C>T |
COCA-CN | 16 | 4394783 | 4394783 | single base substitution | T | C | intron_variant | | |
COCA-CN | 16 | 4407356 | 4407356 | single base substitution | C | T | intron_variant | | |
COCA-CN | 16 | 4408067 | 4408067 | single base substitution | G | A | 3_prime_UTR_variant | | |
COCA-CN | 16 | 4408067 | 4408067 | single base substitution | G | A | exon_variant | | |
COCA-CN | 16 | 4408067 | 4408067 | single base substitution | G | A | missense_variant | A832V | 2495C>T |
COCA-CN | 16 | 4408096 | 4408096 | single base substitution | G | T | 3_prime_UTR_variant | | |
COCA-CN | 16 | 4408096 | 4408096 | single base substitution | G | T | exon_variant | | |
COCA-CN | 16 | 4408096 | 4408096 | single base substitution | G | T | missense_variant | F822L | 2466C>A |
COCA-CN | 16 | 4408299 | 4408299 | single base substitution | C | T | intron_variant | | |
COCA-CN | 16 | 4408326 | 4408326 | single base substitution | G | A | intron_variant | | |
COCA-CN | 16 | 4409296 | 4409296 | single base substitution | C | T | splice_donor_variant | | |
COCA-CN | 16 | 4410881 | 4410881 | single base substitution | A | G | intron_variant | | |
COCA-CN | 16 | 4410881 | 4410881 | single base substitution | A | G | upstream_gene_variant | | |
COCA-CN | 16 | 4410889 | 4410889 | single base substitution | A | T | intron_variant | | |
COCA-CN | 16 | 4410889 | 4410889 | single base substitution | A | T | upstream_gene_variant | | |
COCA-CN | 16 | 4414400 | 4414400 | single base substitution | G | A | exon_variant | | |
COCA-CN | 16 | 4414400 | 4414400 | single base substitution | G | A | synonymous_variant | S384S | 1152C>T |
COCA-CN | 16 | 4414817 | 4414817 | single base substitution | C | T | exon_variant | | |
COCA-CN | 16 | 4414817 | 4414817 | single base substitution | C | T | missense_variant | D335N | 1003G>A |
COCA-CN | 16 | 4431387 | 4431387 | single base substitution | G | A | intron_variant | | |
COCA-CN | 16 | 4431871 | 4431871 | single base substitution | G | A | intron_variant | | |
COCA-CN | 16 | 4432138 | 4432138 | single base substitution | C | T | intron_variant | | |
COCA-CN | 16 | 4432288 | 4432288 | single base substitution | G | A | intron_variant | | |
EOPC-DE | 16 | 4410884 | 4410884 | single base substitution | T | A | intron_variant | | |
EOPC-DE | 16 | 4410884 | 4410884 | single base substitution | T | A | upstream_gene_variant | | |
EOPC-DE | 16 | 4432973 | 4432973 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4390715 | 4390715 | single base substitution | G | A | downstream_gene_variant | | |
ESAD-UK | 16 | 4390715 | 4390715 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4392743 | 4392743 | single base substitution | T | C | intron_variant | | |
ESAD-UK | 16 | 4397137 | 4397137 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4397822 | 4397822 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4398326 | 4398326 | single base substitution | G | C | intron_variant | | |
ESAD-UK | 16 | 4399334 | 4399334 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4402023 | 4402023 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4402159 | 4402159 | single base substitution | C | A | intron_variant | | |
ESAD-UK | 16 | 4405219 | 4405219 | single base substitution | A | C | intron_variant | | |
ESAD-UK | 16 | 4408245 | 4408245 | deletion of <=200bp | G | - | intron_variant | | |
ESAD-UK | 16 | 4412203 | 4412203 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4412203 | 4412203 | single base substitution | G | A | upstream_gene_variant | | |
ESAD-UK | 16 | 4413268 | 4413268 | deletion of <=200bp | A | - | intron_variant | | |
ESAD-UK | 16 | 4413268 | 4413268 | deletion of <=200bp | A | - | upstream_gene_variant | | |
ESAD-UK | 16 | 4416364 | 4416364 | single base substitution | G | T | intron_variant | | |
ESAD-UK | 16 | 4418023 | 4418023 | single base substitution | T | C | intron_variant | | |
ESAD-UK | 16 | 4418694 | 4418694 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4418843 | 4418843 | single base substitution | G | T | intron_variant | | |
ESAD-UK | 16 | 4420661 | 4420661 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4422253 | 4422253 | single base substitution | G | C | intron_variant | | |
ESAD-UK | 16 | 4424599 | 4424599 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4430956 | 4430956 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4437854 | 4437854 | insertion of <=200bp | - | T | intron_variant | | |
ESAD-UK | 16 | 4437856 | 4437856 | single base substitution | G | T | intron_variant | | |
ESAD-UK | 16 | 4437857 | 4437857 | single base substitution | C | A | intron_variant | | |
ESAD-UK | 16 | 4441602 | 4441602 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4443759 | 4443759 | single base substitution | C | G | intron_variant | | |
ESAD-UK | 16 | 4445177 | 4445177 | single base substitution | C | A | intron_variant | | |
ESAD-UK | 16 | 4447800 | 4447800 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4448980 | 4448980 | single base substitution | A | C | intron_variant | | |
ESAD-UK | 16 | 4449040 | 4449040 | single base substitution | G | T | intron_variant | | |
ESAD-UK | 16 | 4449321 | 4449321 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4455057 | 4455057 | single base substitution | T | C | intron_variant | | |
ESAD-UK | 16 | 4456297 | 4456297 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4459367 | 4459367 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4460887 | 4460887 | single base substitution | T | C | intron_variant | | |
ESAD-UK | 16 | 4462207 | 4462207 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4464295 | 4464295 | single base substitution | C | T | intron_variant | | |
ESAD-UK | 16 | 4468072 | 4468072 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4468072 | 4468072 | single base substitution | G | A | upstream_gene_variant | | |
ESAD-UK | 16 | 4468858 | 4468858 | single base substitution | G | C | intron_variant | | |
ESAD-UK | 16 | 4468858 | 4468858 | single base substitution | G | C | upstream_gene_variant | | |
ESAD-UK | 16 | 4469911 | 4469911 | single base substitution | A | G | intron_variant | | |
ESAD-UK | 16 | 4469911 | 4469911 | single base substitution | A | G | upstream_gene_variant | | |
ESAD-UK | 16 | 4470268 | 4470268 | single base substitution | G | A | intron_variant | | |
ESAD-UK | 16 | 4470268 | 4470268 | single base substitution | G | A | upstream_gene_variant | | |
ESAD-UK | 16 | 4470656 | 4470656 | deletion of <=200bp | G | - | upstream_gene_variant | | |
ESAD-UK | 16 | 4473259 | 4473259 | single base substitution | A | T | upstream_gene_variant | | |
ESCA-CN | 16 | 4408376 | 4408376 | single base substitution | G | A | 3_prime_UTR_variant | | |
ESCA-CN | 16 | 4408376 | 4408376 | single base substitution | G | A | exon_variant | | |
ESCA-CN | 16 | 4408376 | 4408376 | single base substitution | G | A | stop_gained | R817* | 2449C>T |
ESCA-CN | 16 | 4410339 | 4410339 | single base substitution | C | T | 3_prime_UTR_variant | | |
ESCA-CN | 16 | 4410339 | 4410339 | single base substitution | C | T | missense_variant | R683H | 2048G>A |
ESCA-CN | 16 | 4410339 | 4410339 | single base substitution | C | T | upstream_gene_variant | | |
ESCA-CN | 16 | 4431503 | 4431503 | single base substitution | G | A | intron_variant | | |
ESCA-CN | 16 | 4432030 | 4432030 | single base substitution | G | A | intron_variant | | |
ESCA-CN | 16 | 4432867 | 4432867 | single base substitution | C | G | intron_variant | | |
ESCA-CN | 16 | 4438627 | 4438627 | single base substitution | C | A | exon_variant | | |
ESCA-CN | 16 | 4438627 | 4438627 | single base substitution | C | A | synonymous_variant | T207T | 621G>T |
GBM-US | 16 | 4391505 | 4391505 | single base substitution | G | C | 3_prime_UTR_variant | | |
GBM-US | 16 | 4391505 | 4391505 | single base substitution | G | C | missense_variant | A953G | 2858C>G |
GBM-US | 16 | 4391505 | 4391505 | single base substitution | G | C | splice_region_variant | | |
GBM-US | 16 | 4411454 | 4411454 | single base substitution | C | T | 3_prime_UTR_variant | | |
GBM-US | 16 | 4411454 | 4411454 | single base substitution | C | T | missense_variant | R532H | 1595G>A |
GBM-US | 16 | 4411454 | 4411454 | single base substitution | C | T | upstream_gene_variant | | |
GBM-US | 16 | 4414382 | 4414382 | single base substitution | C | T | exon_variant | | |
GBM-US | 16 | 4414382 | 4414382 | single base substitution | C | T | synonymous_variant | R390R | 1170G>A |
KIRC-US | 16 | 4405287 | 4405287 | single base substitution | C | A | missense_variant | W924C | 2772G>T |
KIRC-US | 16 | 4405287 | 4405287 | single base substitution | C | A | splice_region_variant | | |
KIRC-US | 16 | 4408461 | 4408461 | single base substitution | C | T | 3_prime_UTR_variant | | |
KIRC-US | 16 | 4408461 | 4408461 | single base substitution | C | T | exon_variant | | |
KIRC-US | 16 | 4408461 | 4408461 | single base substitution | C | T | synonymous_variant | T788T | 2364G>A |
KIRP-US | 16 | 4432543 | 4432543 | single base substitution | A | C | intron_variant | | |
LAML-KR | 16 | 4410884 | 4410884 | single base substitution | T | A | intron_variant | | |
LAML-KR | 16 | 4410884 | 4410884 | single base substitution | T | A | upstream_gene_variant | | |
LAML-KR | 16 | 4413421 | 4413421 | single base substitution | C | A | intron_variant | | |
LAML-KR | 16 | 4413421 | 4413421 | single base substitution | C | A | upstream_gene_variant | | |
LAML-KR | 16 | 4413441 | 4413441 | single base substitution | T | C | intron_variant | | |
LAML-KR | 16 | 4413441 | 4413441 | single base substitution | T | C | upstream_gene_variant | | |
LAML-KR | 16 | 4413668 | 4413668 | single base substitution | G | A | intron_variant | | |
LAML-KR | 16 | 4413668 | 4413668 | single base substitution | G | A | upstream_gene_variant | | |
LAML-KR | 16 | 4474018 | 4474018 | single base substitution | A | G | upstream_gene_variant | | |
LAML-KR | 16 | 4474024 | 4474024 | single base substitution | T | C | upstream_gene_variant | | |
LAML-KR | 16 | 4474030 | 4474030 | single base substitution | C | T | upstream_gene_variant | | |
LGG-US | 16 | 4431389 | 4431391 | deletion of <=200bp | CTG | - | intron_variant | | |
LICA-CN | 16 | 4432288 | 4432288 | single base substitution | G | A | intron_variant | | |
LICA-FR | 16 | 4386772 | 4386772 | single base substitution | T | C | downstream_gene_variant | | |
LICA-FR | 16 | 4394256 | 4394256 | single base substitution | C | T | intron_variant | | |
LICA-FR | 16 | 4394274 | 4394274 | single base substitution | T | C | intron_variant | | |
LICA-FR | 16 | 4394330 | 4394330 | single base substitution | C | T | intron_variant | | |
LICA-FR | 16 | 4394480 | 4394480 | single base substitution | T | C | intron_variant | | |
LICA-FR | 16 | 4394588 | 4394588 | single base substitution | C | T | intron_variant | | |
LICA-FR | 16 | 4394797 | 4394797 | single base substitution | A | G | intron_variant | | |
LICA-FR | 16 | 4410456 | 4410456 | single base substitution | C | A | 3_prime_UTR_variant | | |
LICA-FR | 16 | 4410456 | 4410456 | single base substitution | C | A | stop_gained | E671* | 2011G>T |
LICA-FR | 16 | 4410456 | 4410456 | single base substitution | C | A | upstream_gene_variant | | |
LICA-FR | 16 | 4410467 | 4410483 | deletion of <=200bp | CGGGGCCTGTAGACCCG | - | 3_prime_UTR_variant | | |
LICA-FR | 16 | 4410467 | 4410483 | deletion of <=200bp | CGGGGCCTGTAGACCCG | - | frameshift_variant | RVYRPR662 | |
LICA-FR | 16 | 4410467 | 4410483 | deletion of <=200bp | CGGGGCCTGTAGACCCG | - | upstream_gene_variant | | |
LICA-FR | 16 | 4426902 | 4426902 | single base substitution | T | G | intron_variant | | |
LICA-FR | 16 | 4432636 | 4432636 | single base substitution | C | A | intron_variant | | |
LICA-FR | 16 | 4439472 | 4439472 | single base substitution | G | A | intron_variant | | |
LICA-FR | 16 | 4447017 | 4447017 | insertion of <=200bp | - | A | intron_variant | | |
LICA-FR | 16 | 4464587 | 4464587 | single base substitution | G | A | intron_variant | | |
LICA-FR | 16 | 4471046 | 4471060 | deletion of <=200bp | TGGAATGCAGTGGCG | - | upstream_gene_variant | | |
LIHC-US | 16 | 4431099 | 4431099 | single base substitution | G | T | intron_variant | | |
LIHC-US | 16 | 4432163 | 4432163 | single base substitution | G | A | intron_variant | | |
LINC-JP | 16 | 4390398 | 4390398 | single base substitution | G | A | 3_prime_UTR_variant | | |
LINC-JP | 16 | 4390398 | 4390398 | single base substitution | G | A | downstream_gene_variant | | |
LINC-JP | 16 | 4390398 | 4390398 | single base substitution | G | A | synonymous_variant | R1023R | 3069C>T |
LINC-JP | 16 | 4399263 | 4399263 | single base substitution | T | C | intron_variant | | |
LINC-JP | 16 | 4406886 | 4406886 | single base substitution | C | T | intron_variant | | |
LINC-JP | 16 | 4410862 | 4410862 | single base substitution | A | T | intron_variant | | |
LINC-JP | 16 | 4410862 | 4410862 | single base substitution | A | T | upstream_gene_variant | | |
LINC-JP | 16 | 4412695 | 4412695 | single base substitution | C | T | exon_variant | | |
LINC-JP | 16 | 4412695 | 4412695 | single base substitution | C | T | synonymous_variant | T440T | 1320G>A |
LINC-JP | 16 | 4412695 | 4412695 | single base substitution | C | T | upstream_gene_variant | | |
LINC-JP | 16 | 4414246 | 4414246 | single base substitution | G | T | intron_variant | | |
LINC-JP | 16 | 4414246 | 4414246 | single base substitution | G | T | upstream_gene_variant | | |
LINC-JP | 16 | 4414579 | 4414579 | single base substitution | G | A | intron_variant | | |
LINC-JP | 16 | 4432398 | 4432398 | single base substitution | G | A | intron_variant | | |
LINC-JP | 16 | 4443633 | 4443633 | single base substitution | T | A | intron_variant | | |
LINC-JP | 16 | 4453656 | 4453656 | single base substitution | G | C | intron_variant | | |
LINC-JP | 16 | 4453869 | 4453869 | single base substitution | C | T | intron_variant | | |
LINC-JP | 16 | 4455002 | 4455002 | single base substitution | C | A | intron_variant | | |
LIRI-JP | 16 | 4385822 | 4385822 | single base substitution | A | C | downstream_gene_variant | | |
LIRI-JP | 16 | 4386686 | 4386686 | single base substitution | G | A | downstream_gene_variant | | |
LIRI-JP | 16 | 4388402 | 4388402 | single base substitution | C | T | downstream_gene_variant | | |
LIRI-JP | 16 | 4390241 | 4390241 | single base substitution | C | A | downstream_gene_variant | | |
LIRI-JP | 16 | 4391467 | 4391467 | single base substitution | G | A | 3_prime_UTR_variant | | |
LIRI-JP | 16 | 4391467 | 4391467 | single base substitution | G | A | exon_variant | | |
LIRI-JP | 16 | 4391467 | 4391467 | single base substitution | G | A | missense_variant | H966Y | 2896C>T |
LIRI-JP | 16 | 4393158 | 4393158 | single base substitution | T | A | intron_variant | | |
LIRI-JP | 16 | 4395099 | 4395099 | single base substitution | T | G | intron_variant | | |
LIRI-JP | 16 | 4396005 | 4396005 | single base substitution | T | C | intron_variant | | |
LIRI-JP | 16 | 4398000 | 4398000 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 16 | 4399150 | 4399150 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 16 | 4403219 | 4403219 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4406409 | 4406409 | single base substitution | T | C | intron_variant | | |
LIRI-JP | 16 | 4408435 | 4408435 | single base substitution | A | G | 3_prime_UTR_variant | | |
LIRI-JP | 16 | 4408435 | 4408435 | single base substitution | A | G | exon_variant | | |
LIRI-JP | 16 | 4408435 | 4408435 | single base substitution | A | G | missense_variant | L797P | 2390T>C |
LIRI-JP | 16 | 4412483 | 4412483 | single base substitution | A | G | intron_variant | | |
LIRI-JP | 16 | 4412483 | 4412483 | single base substitution | A | G | upstream_gene_variant | | |
LIRI-JP | 16 | 4412511 | 4412511 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4412511 | 4412511 | single base substitution | C | T | upstream_gene_variant | | |
LIRI-JP | 16 | 4414283 | 4414283 | single base substitution | G | A | exon_variant | | |
LIRI-JP | 16 | 4414283 | 4414283 | single base substitution | G | A | synonymous_variant | D423D | 1269C>T |
LIRI-JP | 16 | 4414283 | 4414283 | single base substitution | G | A | upstream_gene_variant | | |
LIRI-JP | 16 | 4415270 | 4415270 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 16 | 4418953 | 4418953 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4420158 | 4420158 | single base substitution | C | G | intron_variant | | |
LIRI-JP | 16 | 4428059 | 4428059 | single base substitution | C | A | intron_variant | | |
LIRI-JP | 16 | 4428374 | 4428374 | single base substitution | T | A | intron_variant | | |
LIRI-JP | 16 | 4436241 | 4436241 | deletion of <=200bp | T | - | intron_variant | | |
LIRI-JP | 16 | 4442438 | 4442438 | single base substitution | A | C | intron_variant | | |
LIRI-JP | 16 | 4446611 | 4446611 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 16 | 4451018 | 4451018 | single base substitution | G | A | intron_variant | | |
LIRI-JP | 16 | 4452722 | 4452722 | single base substitution | T | C | intron_variant | | |
LIRI-JP | 16 | 4456123 | 4456123 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4459124 | 4459124 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4459336 | 4459336 | single base substitution | C | G | intron_variant | | |
LIRI-JP | 16 | 4459684 | 4459684 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4459805 | 4459805 | single base substitution | A | T | intron_variant | | |
LIRI-JP | 16 | 4460881 | 4460881 | single base substitution | A | G | intron_variant | | |
LIRI-JP | 16 | 4463104 | 4463104 | single base substitution | T | C | intron_variant | | |
LIRI-JP | 16 | 4463685 | 4463685 | single base substitution | C | T | intron_variant | | |
LIRI-JP | 16 | 4469150 | 4469150 | single base substitution | A | G | intron_variant | | |
LIRI-JP | 16 | 4469150 | 4469150 | single base substitution | A | G | upstream_gene_variant | | |
LIRI-JP | 16 | 4469694 | 4469694 | single base substitution | T | C | intron_variant | | |
LIRI-JP | 16 | 4469694 | 4469694 | single base substitution | T | C | upstream_gene_variant | | |
LIRI-JP | 16 | 4470974 | 4470974 | single base substitution | T | C | upstream_gene_variant | | |
LIRI-JP | 16 | 4473791 | 4473791 | single base substitution | G | A | upstream_gene_variant | | |
LIRI-JP | 16 | 4475242 | 4475242 | single base substitution | G | A | upstream_gene_variant | | |
LUSC-KR | 16 | 4385753 | 4385753 | single base substitution | C | A | downstream_gene_variant | | |
LUSC-KR | 16 | 4385837 | 4385837 | single base substitution | A | G | downstream_gene_variant | | |
LUSC-KR | 16 | 4392318 | 4392318 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 16 | 4393404 | 4393404 | single base substitution | G | T | intron_variant | | |
LUSC-KR | 16 | 4405592 | 4405592 | single base substitution | C | A | intron_variant | | |
LUSC-KR | 16 | 4409834 | 4409834 | single base substitution | C | A | intron_variant | | |
LUSC-KR | 16 | 4409834 | 4409834 | single base substitution | C | A | upstream_gene_variant | | |
LUSC-KR | 16 | 4410903 | 4410903 | single base substitution | G | A | intron_variant | | |
LUSC-KR | 16 | 4410903 | 4410903 | single base substitution | G | A | upstream_gene_variant | | |
LUSC-KR | 16 | 4411988 | 4411988 | single base substitution | C | T | missense_variant | E526K | 1576G>A |
LUSC-KR | 16 | 4411988 | 4411988 | single base substitution | C | T | splice_region_variant | | |
LUSC-KR | 16 | 4411988 | 4411988 | single base substitution | C | T | upstream_gene_variant | | |
LUSC-KR | 16 | 4414985 | 4414985 | single base substitution | G | C | intron_variant | | |
LUSC-KR | 16 | 4417089 | 4417089 | single base substitution | G | A | intron_variant | | |
LUSC-KR | 16 | 4418256 | 4418256 | single base substitution | G | C | intron_variant | | |
LUSC-KR | 16 | 4420750 | 4420750 | single base substitution | T | A | intron_variant | | |
LUSC-KR | 16 | 4421889 | 4421889 | single base substitution | G | T | intron_variant | | |
LUSC-KR | 16 | 4425221 | 4425221 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 16 | 4426362 | 4426362 | single base substitution | G | T | intron_variant | | |
LUSC-KR | 16 | 4426519 | 4426519 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 16 | 4434404 | 4434404 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 16 | 4439407 | 4439407 | single base substitution | C | A | intron_variant | | |
LUSC-KR | 16 | 4441571 | 4441571 | single base substitution | C | A | intron_variant | | |
LUSC-KR | 16 | 4441797 | 4441797 | single base substitution | G | A | intron_variant | | |
LUSC-KR | 16 | 4444668 | 4444668 | single base substitution | T | A | intron_variant | | |
LUSC-KR | 16 | 4450372 | 4450372 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 16 | 4451129 | 4451129 | single base substitution | G | T | intron_variant | | |
LUSC-KR | 16 | 4456977 | 4456977 | single base substitution | C | A | intron_variant | | |
LUSC-KR | 16 | 4464985 | 4464985 | single base substitution | C | T | intron_variant | | |
LUSC-KR | 16 | 4466627 | 4466627 | single base substitution | A | G | 5_prime_UTR_premature_start_codon_gain_variant | | |
LUSC-KR | 16 | 4466627 | 4466627 | single base substitution | A | G | upstream_gene_variant | | |
LUSC-KR | 16 | 4471187 | 4471187 | single base substitution | G | T | upstream_gene_variant | | |
LUSC-KR | 16 | 4471301 | 4471301 | single base substitution | G | T | upstream_gene_variant | | |
LUSC-KR | 16 | 4471410 | 4471410 | single base substitution | C | A | upstream_gene_variant | | |
LUSC-KR | 16 | 4471411 | 4471411 | single base substitution | C | A | upstream_gene_variant | | |
LUSC-KR | 16 | 4471535 | 4471535 | single base substitution | C | A | upstream_gene_variant | | |
LUSC-US | 16 | 4385313 | 4385313 | single base substitution | G | T | downstream_gene_variant | | |
LUSC-US | 16 | 4391372 | 4391372 | single base substitution | C | T | 3_prime_UTR_variant | | |
LUSC-US | 16 | 4391372 | 4391372 | single base substitution | C | T | exon_variant | | |
LUSC-US | 16 | 4391372 | 4391372 | single base substitution | C | T | synonymous_variant | Q997Q | 2991G>A |
LUSC-US | 16 | 4407255 | 4407255 | single base substitution | G | A | 3_prime_UTR_variant | | |
LUSC-US | 16 | 4407255 | 4407255 | single base substitution | G | A | exon_variant | | |
LUSC-US | 16 | 4407255 | 4407255 | single base substitution | G | A | stop_gained | Q867* | 2599C>T |
LUSC-US | 16 | 4410973 | 4410973 | single base substitution | G | A | 3_prime_UTR_variant | | |
LUSC-US | 16 | 4410973 | 4410973 | single base substitution | G | A | missense_variant | R630W | 1888C>T |
LUSC-US | 16 | 4410973 | 4410973 | single base substitution | G | A | upstream_gene_variant | | |
LUSC-US | 16 | 4411466 | 4411466 | single base substitution | C | T | 3_prime_UTR_variant | | |
LUSC-US | 16 | 4411466 | 4411466 | single base substitution | C | T | missense_variant | R528Q | 1583G>A |
LUSC-US | 16 | 4411466 | 4411466 | single base substitution | C | T | upstream_gene_variant | | |
LUSC-US | 16 | 4414342 | 4414342 | deletion of <=200bp | C | - | exon_variant | | |
LUSC-US | 16 | 4414342 | 4414342 | deletion of <=200bp | C | - | frameshift_variant | E404 | |
LUSC-US | 16 | 4414342 | 4414342 | deletion of <=200bp | C | - | upstream_gene_variant | | |
LUSC-US | 16 | 4414874 | 4414874 | single base substitution | G | C | exon_variant | | |
LUSC-US | 16 | 4414874 | 4414874 | single base substitution | G | C | missense_variant | P316A | 946C>G |
LUSC-US | 16 | 4415002 | 4415002 | single base substitution | A | T | splice_donor_variant | | |
LUSC-US | 16 | 4415025 | 4415025 | single base substitution | G | A | exon_variant | | |
LUSC-US | 16 | 4415025 | 4415025 | single base substitution | G | A | stop_gained | Q293* | 877C>T |
LUSC-US | 16 | 4431739 | 4431739 | single base substitution | C | A | intron_variant | | |
LUSC-US | 16 | 4431778 | 4431778 | single base substitution | C | T | intron_variant | | |
MALY-DE | 16 | 4386157 | 4386157 | insertion of <=200bp | - | T | downstream_gene_variant | | |
MALY-DE | 16 | 4396715 | 4396715 | single base substitution | C | G | intron_variant | | |
MALY-DE | 16 | 4420616 | 4420616 | single base substitution | C | A | intron_variant | | |
MALY-DE | 16 | 4426651 | 4426651 | single base substitution | G | A | intron_variant | | |
MALY-DE | 16 | 4430428 | 4430428 | single base substitution | C | T | intron_variant | | |
MALY-DE | 16 | 4446485 | 4446485 | single base substitution | T | C | intron_variant | | |
MALY-DE | 16 | 4453083 | 4453083 | single base substitution | G | T | intron_variant | | |
MALY-DE | 16 | 4453569 | 4453569 | single base substitution | A | G | intron_variant | | |
MALY-DE | 16 | 4469218 | 4469218 | single base substitution | T | C | intron_variant | | |
MALY-DE | 16 | 4469218 | 4469218 | single base substitution | T | C | upstream_gene_variant | | |
MELA-AU | 16 | 4385332 | 4385332 | single base substitution | C | T | downstream_gene_variant | | |
MELA-AU | 16 | 4385353 | 4385354 | multiple base substitution (>=2bp and <=200bp) | CC | TT | downstream_gene_variant | | |
MELA-AU | 16 | 4385468 | 4385468 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 16 | 4386196 | 4386197 | multiple base substitution (>=2bp and <=200bp) | GG | CA | downstream_gene_variant | | |
MELA-AU | 16 | 4386426 | 4386426 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 16 | 4386449 | 4386449 | single base substitution | C | T | downstream_gene_variant | | |
MELA-AU | 16 | 4387343 | 4387344 | multiple base substitution (>=2bp and <=200bp) | CT | TA | downstream_gene_variant | | |
MELA-AU | 16 | 4387965 | 4387965 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 16 | 4388348 | 4388349 | multiple base substitution (>=2bp and <=200bp) | CC | TT | downstream_gene_variant | | |
MELA-AU | 16 | 4388554 | 4388555 | multiple base substitution (>=2bp and <=200bp) | GG | AA | downstream_gene_variant | | |
MELA-AU | 16 | 4388736 | 4388736 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 16 | 4389198 | 4389198 | single base substitution | C | T | downstream_gene_variant | | |
MELA-AU | 16 | 4390246 | 4390246 | single base substitution | G | A | downstream_gene_variant | | |
MELA-AU | 16 | 4390952 | 4390952 | single base substitution | G | A | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4390952 | 4390952 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4390952 | 4390952 | single base substitution | G | A | missense_variant | S1010F | 3029C>T |
MELA-AU | 16 | 4391082 | 4391083 | multiple base substitution (>=2bp and <=200bp) | CC | TT | intron_variant | | |
MELA-AU | 16 | 4391091 | 4391091 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4391462 | 4391462 | single base substitution | C | T | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4391462 | 4391462 | single base substitution | C | T | exon_variant | | |
MELA-AU | 16 | 4391462 | 4391462 | single base substitution | C | T | synonymous_variant | R967R | 2901G>A |
MELA-AU | 16 | 4391768 | 4391768 | single base substitution | G | T | intron_variant | | |
MELA-AU | 16 | 4391848 | 4391848 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4393106 | 4393106 | single base substitution | C | G | intron_variant | | |
MELA-AU | 16 | 4393239 | 4393239 | single base substitution | G | A | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4393239 | 4393239 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4393239 | 4393239 | single base substitution | G | A | synonymous_variant | A942A | 2826C>T |
MELA-AU | 16 | 4395315 | 4395315 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4395747 | 4395747 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4395779 | 4395779 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4395839 | 4395839 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4396052 | 4396052 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4396131 | 4396132 | multiple base substitution (>=2bp and <=200bp) | GG | AT | intron_variant | | |
MELA-AU | 16 | 4396319 | 4396319 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4397581 | 4397582 | multiple base substitution (>=2bp and <=200bp) | CC | TT | intron_variant | | |
MELA-AU | 16 | 4398637 | 4398638 | multiple base substitution (>=2bp and <=200bp) | CC | AT | intron_variant | | |
MELA-AU | 16 | 4399901 | 4399901 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4400099 | 4400099 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4400326 | 4400326 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4401333 | 4401333 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4401415 | 4401415 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4401951 | 4401951 | single base substitution | C | G | intron_variant | | |
MELA-AU | 16 | 4402126 | 4402126 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4402511 | 4402511 | single base substitution | A | G | intron_variant | | |
MELA-AU | 16 | 4402988 | 4402988 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4403148 | 4403148 | insertion of <=200bp | - | A | intron_variant | | |
MELA-AU | 16 | 4403604 | 4403604 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4403811 | 4403812 | multiple base substitution (>=2bp and <=200bp) | CC | TT | intron_variant | | |
MELA-AU | 16 | 4404405 | 4404405 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4404860 | 4404860 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4404887 | 4404887 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4405105 | 4405105 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4405172 | 4405172 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4405214 | 4405214 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4405315 | 4405315 | single base substitution | G | A | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4405315 | 4405315 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4405315 | 4405315 | single base substitution | G | A | missense_variant | S915F | 2744C>T |
MELA-AU | 16 | 4405326 | 4405326 | single base substitution | G | A | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4405326 | 4405326 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4405326 | 4405326 | single base substitution | G | A | synonymous_variant | L911L | 2733C>T |
MELA-AU | 16 | 4405405 | 4405405 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4405406 | 4405406 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4405663 | 4405663 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4407777 | 4407777 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4407962 | 4407963 | multiple base substitution (>=2bp and <=200bp) | GG | AA | splice_region_variant | | |
MELA-AU | 16 | 4408498 | 4408498 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4409006 | 4409006 | single base substitution | G | T | intron_variant | | |
MELA-AU | 16 | 4409246 | 4409246 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4409336 | 4409336 | single base substitution | G | A | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4409336 | 4409336 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4409336 | 4409336 | single base substitution | G | A | synonymous_variant | F767F | 2301C>T |
MELA-AU | 16 | 4409368 | 4409368 | single base substitution | G | A | 3_prime_UTR_variant | | |
MELA-AU | 16 | 4409368 | 4409368 | single base substitution | G | A | synonymous_variant | L757L | 2269C>T |
MELA-AU | 16 | 4409368 | 4409368 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4409393 | 4409393 | single base substitution | G | A | splice_region_variant | | |
MELA-AU | 16 | 4409393 | 4409393 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4411318 | 4411318 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4411318 | 4411318 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4412197 | 4412197 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4412197 | 4412197 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4412869 | 4412869 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4412869 | 4412869 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4412937 | 4412937 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4412937 | 4412937 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4413013 | 4413013 | single base substitution | A | C | intron_variant | | |
MELA-AU | 16 | 4413013 | 4413013 | single base substitution | A | C | upstream_gene_variant | | |
MELA-AU | 16 | 4414250 | 4414250 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4414250 | 4414250 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4414361 | 4414361 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4414361 | 4414361 | single base substitution | G | A | synonymous_variant | S397S | 1191C>T |
MELA-AU | 16 | 4414496 | 4414496 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4414497 | 4414497 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4414504 | 4414504 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4414836 | 4414836 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4414836 | 4414836 | single base substitution | G | A | synonymous_variant | L328L | 984C>T |
MELA-AU | 16 | 4415108 | 4415109 | multiple base substitution (>=2bp and <=200bp) | GG | AA | intron_variant | | |
MELA-AU | 16 | 4415179 | 4415179 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4415224 | 4415224 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4415796 | 4415796 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4415805 | 4415805 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4415911 | 4415911 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4416880 | 4416880 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4417670 | 4417670 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4418045 | 4418045 | single base substitution | A | C | intron_variant | | |
MELA-AU | 16 | 4418110 | 4418110 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4418833 | 4418833 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4419463 | 4419463 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4421705 | 4421705 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4421734 | 4421734 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4422244 | 4422244 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4423160 | 4423160 | single base substitution | A | G | intron_variant | | |
MELA-AU | 16 | 4423452 | 4423452 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4424525 | 4424525 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4424548 | 4424548 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4425178 | 4425178 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4425391 | 4425391 | deletion of <=200bp | T | - | intron_variant | | |
MELA-AU | 16 | 4426194 | 4426194 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4428342 | 4428342 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4430134 | 4430134 | single base substitution | T | C | intron_variant | | |
MELA-AU | 16 | 4430823 | 4430823 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4431796 | 4431796 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4432552 | 4432552 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4433523 | 4433523 | single base substitution | T | A | intron_variant | | |
MELA-AU | 16 | 4434042 | 4434042 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4435077 | 4435077 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4435144 | 4435144 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4435564 | 4435564 | single base substitution | C | A | intron_variant | | |
MELA-AU | 16 | 4436017 | 4436017 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4436053 | 4436053 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4436091 | 4436091 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4437256 | 4437256 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4437387 | 4437387 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4437805 | 4437805 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4438137 | 4438137 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4438220 | 4438220 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4438281 | 4438281 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4438303 | 4438303 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4438534 | 4438534 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4438579 | 4438580 | multiple base substitution (>=2bp and <=200bp) | GG | AA | exon_variant | | |
MELA-AU | 16 | 4438579 | 4438580 | multiple base substitution (>=2bp and <=200bp) | GG | AA | missense_variant | T223I | 668CC>TT |
MELA-AU | 16 | 4438650 | 4438650 | single base substitution | T | A | intron_variant | | |
MELA-AU | 16 | 4438923 | 4438923 | single base substitution | C | A | intron_variant | | |
MELA-AU | 16 | 4439137 | 4439137 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4439959 | 4439959 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4440156 | 4440156 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4440289 | 4440289 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4441234 | 4441234 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4442165 | 4442165 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4442380 | 4442380 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4442444 | 4442444 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4443080 | 4443080 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4443114 | 4443114 | single base substitution | A | G | intron_variant | | |
MELA-AU | 16 | 4443157 | 4443157 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4443678 | 4443678 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4443943 | 4443943 | single base substitution | T | A | intron_variant | | |
MELA-AU | 16 | 4443968 | 4443968 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4444309 | 4444309 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445162 | 4445162 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445163 | 4445163 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445354 | 4445354 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445377 | 4445378 | multiple base substitution (>=2bp and <=200bp) | GG | AA | intron_variant | | |
MELA-AU | 16 | 4445386 | 4445386 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445529 | 4445529 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4445791 | 4445791 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445899 | 4445899 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4445970 | 4445970 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4446216 | 4446216 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4447371 | 4447371 | single base substitution | G | T | intron_variant | | |
MELA-AU | 16 | 4447596 | 4447596 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4447656 | 4447656 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4448927 | 4448927 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4449258 | 4449258 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4449491 | 4449491 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4450043 | 4450043 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4450426 | 4450426 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4451135 | 4451135 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4451168 | 4451168 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4451977 | 4451977 | single base substitution | T | C | intron_variant | | |
MELA-AU | 16 | 4452994 | 4452994 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4453323 | 4453323 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4453517 | 4453517 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4453586 | 4453586 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4453670 | 4453670 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4453681 | 4453681 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4453992 | 4453992 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4454279 | 4454279 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4454719 | 4454719 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4455351 | 4455351 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4455696 | 4455696 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4455698 | 4455698 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4456080 | 4456080 | single base substitution | A | G | intron_variant | | |
MELA-AU | 16 | 4456085 | 4456086 | multiple base substitution (>=2bp and <=200bp) | CC | TT | intron_variant | | |
MELA-AU | 16 | 4457174 | 4457174 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4457475 | 4457475 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4457851 | 4457851 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4457909 | 4457909 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4457926 | 4457926 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4458281 | 4458281 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4459121 | 4459121 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4459778 | 4459779 | multiple base substitution (>=2bp and <=200bp) | GA | AC | intron_variant | | |
MELA-AU | 16 | 4461560 | 4461560 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4462496 | 4462496 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4462634 | 4462634 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4462712 | 4462712 | single base substitution | G | C | intron_variant | | |
MELA-AU | 16 | 4462876 | 4462876 | single base substitution | A | C | intron_variant | | |
MELA-AU | 16 | 4463368 | 4463368 | single base substitution | G | A | exon_variant | | |
MELA-AU | 16 | 4463368 | 4463368 | single base substitution | G | A | missense_variant | S33L | 98C>T |
MELA-AU | 16 | 4463487 | 4463487 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4466328 | 4466328 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4466599 | 4466599 | single base substitution | C | T | 5_prime_UTR_variant | | |
MELA-AU | 16 | 4466599 | 4466599 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4466714 | 4466714 | single base substitution | C | T | 5_prime_UTR_variant | | |
MELA-AU | 16 | 4466714 | 4466714 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4466889 | 4466889 | single base substitution | G | A | 5_prime_UTR_premature_start_codon_gain_variant | | |
MELA-AU | 16 | 4466889 | 4466889 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4467217 | 4467217 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4467217 | 4467217 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4467277 | 4467277 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4467277 | 4467277 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4467428 | 4467428 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4467428 | 4467428 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4468121 | 4468121 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4468121 | 4468121 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4468663 | 4468663 | single base substitution | A | T | intron_variant | | |
MELA-AU | 16 | 4468663 | 4468663 | single base substitution | A | T | upstream_gene_variant | | |
MELA-AU | 16 | 4469476 | 4469476 | single base substitution | T | C | intron_variant | | |
MELA-AU | 16 | 4469476 | 4469476 | single base substitution | T | C | upstream_gene_variant | | |
MELA-AU | 16 | 4469627 | 4469627 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4469627 | 4469627 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4469764 | 4469764 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4469764 | 4469764 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4469833 | 4469833 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4469833 | 4469833 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4469834 | 4469834 | single base substitution | G | A | intron_variant | | |
MELA-AU | 16 | 4469834 | 4469834 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4469925 | 4469925 | single base substitution | C | T | intron_variant | | |
MELA-AU | 16 | 4469925 | 4469925 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4470591 | 4470591 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4471583 | 4471583 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4472499 | 4472499 | single base substitution | G | A | upstream_gene_variant | | |
MELA-AU | 16 | 4473216 | 4473217 | multiple base substitution (>=2bp and <=200bp) | CC | AT | upstream_gene_variant | | |
MELA-AU | 16 | 4473246 | 4473246 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4473342 | 4473342 | insertion of <=200bp | - | T | upstream_gene_variant | | |
MELA-AU | 16 | 4473409 | 4473409 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4473995 | 4473995 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4474206 | 4474206 | single base substitution | C | T | upstream_gene_variant | | |
MELA-AU | 16 | 4474896 | 4474896 | single base substitution | C | G | upstream_gene_variant | | |
ORCA-IN | 16 | 4389371 | 4389371 | single base substitution | C | T | downstream_gene_variant | | |
ORCA-IN | 16 | 4396884 | 4396884 | single base substitution | C | G | intron_variant | | |
ORCA-IN | 16 | 4402899 | 4402899 | single base substitution | C | T | intron_variant | | |
ORCA-IN | 16 | 4403356 | 4403356 | single base substitution | C | G | intron_variant | | |
ORCA-IN | 16 | 4404159 | 4404159 | single base substitution | C | G | intron_variant | | |
ORCA-IN | 16 | 4407230 | 4407230 | single base substitution | C | T | 3_prime_UTR_variant | | |
ORCA-IN | 16 | 4407230 | 4407230 | single base substitution | C | T | exon_variant | | |
ORCA-IN | 16 | 4407230 | 4407230 | single base substitution | C | T | missense_variant | R875H | 2624G>A |
ORCA-IN | 16 | 4408462 | 4408462 | single base substitution | G | A | 3_prime_UTR_variant | | |
ORCA-IN | 16 | 4408462 | 4408462 | single base substitution | G | A | exon_variant | | |
ORCA-IN | 16 | 4408462 | 4408462 | single base substitution | G | A | missense_variant | T788M | 2363C>T |
ORCA-IN | 16 | 4430096 | 4430096 | single base substitution | G | C | intron_variant | | |
ORCA-IN | 16 | 4432684 | 4432684 | single base substitution | G | T | intron_variant | | |
ORCA-IN | 16 | 4432808 | 4432808 | single base substitution | G | T | intron_variant | | |
ORCA-IN | 16 | 4438106 | 4438106 | single base substitution | G | A | intron_variant | | |
ORCA-IN | 16 | 4455820 | 4455821 | multiple base substitution (>=2bp and <=200bp) | TC | CA | intron_variant | | |
OV-AU | 16 | 4386282 | 4386282 | single base substitution | G | C | downstream_gene_variant | | |
OV-AU | 16 | 4391917 | 4391917 | single base substitution | C | T | intron_variant | | |
OV-AU | 16 | 4392664 | 4392664 | single base substitution | A | G | intron_variant | | |
OV-AU | 16 | 4395298 | 4395298 | single base substitution | C | G | intron_variant | | |
OV-AU | 16 | 4395623 | 4395623 | single base substitution | T | C | intron_variant | | |
OV-AU | 16 | 4402158 | 4402158 | single base substitution | A | T | intron_variant | | |
OV-AU | 16 | 4407326 | 4407326 | single base substitution | C | T | intron_variant | | |
OV-AU | 16 | 4415472 | 4415472 | single base substitution | A | C | intron_variant | | |
OV-AU | 16 | 4416351 | 4416351 | single base substitution | C | T | intron_variant | | |
OV-AU | 16 | 4417632 | 4417632 | single base substitution | G | T | intron_variant | | |
OV-AU | 16 | 4418491 | 4418491 | single base substitution | G | T | intron_variant | | |
OV-AU | 16 | 4420568 | 4420568 | single base substitution | G | A | intron_variant | | |
OV-AU | 16 | 4421100 | 4421100 | single base substitution | G | A | intron_variant | | |
OV-AU | 16 | 4424405 | 4424405 | single base substitution | T | G | intron_variant | | |
OV-AU | 16 | 4435487 | 4435487 | single base substitution | C | T | intron_variant | | |
OV-AU | 16 | 4445234 | 4445234 | single base substitution | G | C | intron_variant | | |
OV-AU | 16 | 4449321 | 4449321 | single base substitution | C | T | intron_variant | | |
OV-AU | 16 | 4449735 | 4449735 | single base substitution | T | G | intron_variant | | |
OV-AU | 16 | 4464351 | 4464351 | single base substitution | C | T | intron_variant | | |
OV-AU | 16 | 4464712 | 4464712 | single base substitution | T | C | intron_variant | | |
OV-AU | 16 | 4465632 | 4465632 | single base substitution | G | T | intron_variant | | |
OV-AU | 16 | 4468267 | 4468267 | single base substitution | C | G | intron_variant | | |
OV-AU | 16 | 4468267 | 4468267 | single base substitution | C | G | upstream_gene_variant | | |
OV-AU | 16 | 4469018 | 4469018 | single base substitution | G | A | intron_variant | | |
OV-AU | 16 | 4469018 | 4469018 | single base substitution | G | A | upstream_gene_variant | | |
OV-AU | 16 | 4469572 | 4469572 | single base substitution | C | A | intron_variant | | |
OV-AU | 16 | 4469572 | 4469572 | single base substitution | C | A | upstream_gene_variant | | |
OV-AU | 16 | 4470334 | 4470334 | single base substitution | A | G | intron_variant | | |
OV-AU | 16 | 4470334 | 4470334 | single base substitution | A | G | upstream_gene_variant | | |
OV-AU | 16 | 4471389 | 4471389 | single base substitution | C | G | upstream_gene_variant | | |
PACA-AU | 16 | 4387259 | 4387259 | single base substitution | G | A | downstream_gene_variant | | |
PACA-AU | 16 | 4389392 | 4389392 | single base substitution | C | G | downstream_gene_variant | | |
PACA-AU | 16 | 4395132 | 4395132 | single base substitution | G | A | intron_variant | | |
PACA-AU | 16 | 4395656 | 4395656 | single base substitution | A | T | intron_variant | | |
PACA-AU | 16 | 4413500 | 4413500 | single base substitution | G | A | intron_variant | | |
PACA-AU | 16 | 4413500 | 4413500 | single base substitution | G | A | upstream_gene_variant | | |
PACA-AU | 16 | 4415034 | 4415034 | single base substitution | C | A | exon_variant | | |
PACA-AU | 16 | 4415034 | 4415034 | single base substitution | C | A | missense_variant | V290L | 868G>T |
PACA-AU | 16 | 4419839 | 4419839 | single base substitution | A | T | intron_variant | | |
PACA-AU | 16 | 4424784 | 4424784 | single base substitution | G | C | intron_variant | | |
PACA-AU | 16 | 4424926 | 4424926 | single base substitution | G | A | intron_variant | | |
PACA-AU | 16 | 4426180 | 4426181 | deletion of <=200bp | CC | - | intron_variant | | |
PACA-AU | 16 | 4429137 | 4429137 | single base substitution | G | A | intron_variant | | |
PACA-AU | 16 | 4431389 | 4431391 | deletion of <=200bp | CTG | - | intron_variant | | |
PACA-AU | 16 | 4434631 | 4434631 | single base substitution | C | T | intron_variant | | |
PACA-AU | 16 | 4435959 | 4435959 | single base substitution | G | A | intron_variant | | |
PACA-AU | 16 | 4436162 | 4436162 | single base substitution | G | T | intron_variant | | |
PACA-AU | 16 | 4438745 | 4438745 | single base substitution | C | T | intron_variant | | |
PACA-AU | 16 | 4449217 | 4449217 | single base substitution | C | T | intron_variant | | |
PACA-AU | 16 | 4450281 | 4450281 | single base substitution | C | T | intron_variant | | |
PACA-AU | 16 | 4454354 | 4454354 | single base substitution | C | T | intron_variant | | |
PACA-AU | 16 | 4456971 | 4456971 | single base substitution | C | T | intron_variant | | |
PACA-AU | 16 | 4461559 | 4461559 | single base substitution | T | A | intron_variant | | |
PACA-AU | 16 | 4474109 | 4474109 | single base substitution | G | A | upstream_gene_variant | | |
PACA-AU | 16 | 4474279 | 4474279 | single base substitution | T | C | upstream_gene_variant | | |
PACA-AU | 16 | 4474521 | 4474521 | single base substitution | G | A | upstream_gene_variant | | |
PACA-CA | 16 | 4389207 | 4389207 | single base substitution | G | A | downstream_gene_variant | | |
PACA-CA | 16 | 4389331 | 4389331 | single base substitution | C | T | downstream_gene_variant | | |
PACA-CA | 16 | 4392796 | 4392796 | single base substitution | C | G | intron_variant | | |
PACA-CA | 16 | 4395708 | 4395708 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4395961 | 4395961 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4396533 | 4396533 | single base substitution | C | G | intron_variant | | |
PACA-CA | 16 | 4396571 | 4396571 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4399501 | 4399501 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4406115 | 4406115 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4407107 | 4407107 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4413297 | 4413298 | deletion of <=200bp | GT | - | intron_variant | | |
PACA-CA | 16 | 4413297 | 4413298 | deletion of <=200bp | GT | - | upstream_gene_variant | | |
PACA-CA | 16 | 4413472 | 4413472 | single base substitution | C | A | intron_variant | | |
PACA-CA | 16 | 4413472 | 4413472 | single base substitution | C | A | upstream_gene_variant | | |
PACA-CA | 16 | 4414526 | 4414526 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4415429 | 4415429 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4417306 | 4417306 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4420865 | 4420865 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4423889 | 4423889 | single base substitution | A | C | intron_variant | | |
PACA-CA | 16 | 4427225 | 4427225 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4427823 | 4427823 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4429116 | 4429116 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4431360 | 4431360 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4439492 | 4439492 | single base substitution | A | C | intron_variant | | |
PACA-CA | 16 | 4442853 | 4442853 | single base substitution | C | G | intron_variant | | |
PACA-CA | 16 | 4443630 | 4443630 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4444527 | 4444527 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4449447 | 4449447 | single base substitution | G | A | intron_variant | | |
PACA-CA | 16 | 4451197 | 4451197 | single base substitution | G | T | intron_variant | | |
PACA-CA | 16 | 4452242 | 4452242 | insertion of <=200bp | - | TTG | intron_variant | | |
PACA-CA | 16 | 4454084 | 4454084 | single base substitution | A | C | intron_variant | | |
PACA-CA | 16 | 4458430 | 4458430 | deletion of <=200bp | C | - | intron_variant | | |
PACA-CA | 16 | 4465678 | 4465678 | single base substitution | C | G | intron_variant | | |
PACA-CA | 16 | 4466956 | 4466956 | single base substitution | C | T | 5_prime_UTR_variant | | |
PACA-CA | 16 | 4466956 | 4466956 | single base substitution | C | T | upstream_gene_variant | | |
PACA-CA | 16 | 4468713 | 4468713 | single base substitution | C | T | intron_variant | | |
PACA-CA | 16 | 4468713 | 4468713 | single base substitution | C | T | upstream_gene_variant | | |
PACA-CA | 16 | 4474893 | 4474893 | single base substitution | T | A | upstream_gene_variant | | |
PAEN-AU | 16 | 4446640 | 4446640 | single base substitution | T | C | intron_variant | | |
PAEN-AU | 16 | 4466654 | 4466654 | single base substitution | C | T | 5_prime_UTR_variant | | |
PAEN-AU | 16 | 4466654 | 4466654 | single base substitution | C | T | upstream_gene_variant | | |
PAEN-AU | 16 | 4472893 | 4472893 | single base substitution | A | G | upstream_gene_variant | | |
PBCA-DE | 16 | 4389690 | 4389690 | single base substitution | C | T | downstream_gene_variant | | |
PBCA-DE | 16 | 4390120 | 4390120 | single base substitution | C | T | downstream_gene_variant | | |
PBCA-DE | 16 | 4401483 | 4401483 | single base substitution | A | G | intron_variant | | |
PBCA-DE | 16 | 4416519 | 4416519 | single base substitution | C | T | intron_variant | | |
PBCA-DE | 16 | 4417435 | 4417435 | single base substitution | C | T | intron_variant | | |
PBCA-DE | 16 | 4425551 | 4425551 | insertion of <=200bp | - | C | intron_variant | | |
PBCA-DE | 16 | 4429004 | 4429004 | single base substitution | C | T | intron_variant | | |
PBCA-DE | 16 | 4434400 | 4434400 | single base substitution | G | A | intron_variant | | |
PBCA-DE | 16 | 4444564 | 4444564 | single base substitution | C | T | intron_variant | | |
PBCA-DE | 16 | 4452009 | 4452009 | single base substitution | G | C | intron_variant | | |
PBCA-DE | 16 | 4464091 | 4464091 | single base substitution | C | T | intron_variant | | |
PBCA-DE | 16 | 4465798 | 4465798 | single base substitution | C | G | intron_variant | | |
PBCA-DE | 16 | 4466412 | 4466412 | single base substitution | C | T | intron_variant | | |
PBCA-DE | 16 | 4471597 | 4471597 | single base substitution | G | A | upstream_gene_variant | | |
PRAD-CA | 16 | 4399901 | 4399901 | single base substitution | G | T | intron_variant | | |
PRAD-CA | 16 | 4407001 | 4407001 | single base substitution | T | C | intron_variant | | |
PRAD-CA | 16 | 4419117 | 4419117 | single base substitution | C | G | intron_variant | | |
PRAD-CA | 16 | 4428235 | 4428235 | single base substitution | G | A | intron_variant | | |
PRAD-CA | 16 | 4428884 | 4428884 | single base substitution | G | A | intron_variant | | |
PRAD-CA | 16 | 4429501 | 4429501 | single base substitution | G | A | intron_variant | | |
PRAD-CA | 16 | 4440949 | 4440949 | single base substitution | G | A | intron_variant | | |
PRAD-CA | 16 | 4441880 | 4441880 | single base substitution | A | G | intron_variant | | |
PRAD-CA | 16 | 4450502 | 4450502 | single base substitution | C | T | intron_variant | | |
PRAD-CA | 16 | 4458781 | 4458781 | single base substitution | C | T | intron_variant | | |
PRAD-CA | 16 | 4467902 | 4467902 | single base substitution | T | C | intron_variant | | |
PRAD-CA | 16 | 4467902 | 4467902 | single base substitution | T | C | upstream_gene_variant | | |
PRAD-UK | 16 | 4420231 | 4420231 | single base substitution | G | A | intron_variant | | |
PRAD-UK | 16 | 4423116 | 4423116 | deletion of <=200bp | A | - | intron_variant | | |
PRAD-UK | 16 | 4444932 | 4444932 | single base substitution | T | C | intron_variant | | |
PRAD-UK | 16 | 4450793 | 4450793 | single base substitution | C | A | intron_variant | | |
PRAD-UK | 16 | 4469712 | 4469712 | single base substitution | C | T | intron_variant | | |
PRAD-UK | 16 | 4469712 | 4469712 | single base substitution | C | T | upstream_gene_variant | | |
READ-US | 16 | 4393260 | 4393260 | single base substitution | G | A | 3_prime_UTR_variant | | |
READ-US | 16 | 4393260 | 4393260 | single base substitution | G | A | intron_variant | | |
READ-US | 16 | 4393260 | 4393260 | single base substitution | G | A | synonymous_variant | G935G | 2805C>T |
READ-US | 16 | 4411003 | 4411003 | single base substitution | G | T | 3_prime_UTR_variant | | |
READ-US | 16 | 4411003 | 4411003 | single base substitution | G | T | missense_variant | R620S | 1858C>A |
READ-US | 16 | 4411003 | 4411003 | single base substitution | G | T | upstream_gene_variant | | |
READ-US | 16 | 4432065 | 4432065 | single base substitution | C | A | intron_variant | | |
READ-US | 16 | 4455502 | 4455502 | single base substitution | G | A | exon_variant | | |
READ-US | 16 | 4455502 | 4455502 | single base substitution | G | A | missense_variant | T185M | 554C>T |
RECA-EU | 16 | 4388770 | 4388770 | single base substitution | C | A | downstream_gene_variant | | |
RECA-EU | 16 | 4405590 | 4405590 | single base substitution | C | T | intron_variant | | |
RECA-EU | 16 | 4409583 | 4409583 | single base substitution | G | C | 3_prime_UTR_variant | | |
RECA-EU | 16 | 4409583 | 4409583 | single base substitution | G | C | synonymous_variant | A716A | 2148C>G |
RECA-EU | 16 | 4409583 | 4409583 | single base substitution | G | C | upstream_gene_variant | | |
RECA-EU | 16 | 4410123 | 4410123 | single base substitution | C | T | intron_variant | | |
RECA-EU | 16 | 4410123 | 4410123 | single base substitution | C | T | upstream_gene_variant | | |
RECA-EU | 16 | 4412210 | 4412210 | single base substitution | C | A | intron_variant | | |
RECA-EU | 16 | 4412210 | 4412210 | single base substitution | C | A | upstream_gene_variant | | |
RECA-EU | 16 | 4412647 | 4412647 | single base substitution | G | T | exon_variant | | |
RECA-EU | 16 | 4412647 | 4412647 | single base substitution | G | T | synonymous_variant | T456T | 1368C>A |
RECA-EU | 16 | 4412647 | 4412647 | single base substitution | G | T | upstream_gene_variant | | |
RECA-EU | 16 | 4417658 | 4417658 | single base substitution | A | G | intron_variant | | |
RECA-EU | 16 | 4447028 | 4447028 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4385472 | 4385472 | single base substitution | A | G | downstream_gene_variant | | |
SKCA-BR | 16 | 4386949 | 4386949 | single base substitution | A | C | downstream_gene_variant | | |
SKCA-BR | 16 | 4388638 | 4388638 | single base substitution | T | G | downstream_gene_variant | | |
SKCA-BR | 16 | 4390299 | 4390299 | single base substitution | T | G | 3_prime_UTR_variant | | |
SKCA-BR | 16 | 4390299 | 4390299 | single base substitution | T | G | downstream_gene_variant | | |
SKCA-BR | 16 | 4392498 | 4392498 | single base substitution | A | T | intron_variant | | |
SKCA-BR | 16 | 4399203 | 4399203 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4399494 | 4399494 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4400311 | 4400311 | insertion of <=200bp | - | GTA | intron_variant | | |
SKCA-BR | 16 | 4401081 | 4401081 | single base substitution | T | C | intron_variant | | |
SKCA-BR | 16 | 4401127 | 4401127 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4401323 | 4401323 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4402816 | 4402816 | insertion of <=200bp | - | CT | intron_variant | | |
SKCA-BR | 16 | 4408312 | 4408312 | single base substitution | C | T | intron_variant | | |
SKCA-BR | 16 | 4408313 | 4408313 | single base substitution | C | T | intron_variant | | |
SKCA-BR | 16 | 4410867 | 4410889 | deletion of <=200bp | TCACTGCTGGCCCCACCTCTCCA | - | intron_variant | | |
SKCA-BR | 16 | 4410867 | 4410889 | deletion of <=200bp | TCACTGCTGGCCCCACCTCTCCA | - | upstream_gene_variant | | |
SKCA-BR | 16 | 4411844 | 4411844 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4411844 | 4411844 | single base substitution | T | G | upstream_gene_variant | | |
SKCA-BR | 16 | 4411852 | 4411852 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4411852 | 4411852 | single base substitution | A | G | upstream_gene_variant | | |
SKCA-BR | 16 | 4412029 | 4412029 | single base substitution | G | A | exon_variant | | |
SKCA-BR | 16 | 4412029 | 4412029 | single base substitution | G | A | missense_variant | A512V | 1535C>T |
SKCA-BR | 16 | 4412029 | 4412029 | single base substitution | G | A | upstream_gene_variant | | |
SKCA-BR | 16 | 4417100 | 4417100 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4417719 | 4417719 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4419463 | 4419463 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4422065 | 4422065 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4422167 | 4422167 | single base substitution | T | C | intron_variant | | |
SKCA-BR | 16 | 4424187 | 4424187 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4424197 | 4424197 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4425907 | 4425907 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4426079 | 4426079 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4428460 | 4428460 | single base substitution | A | C | intron_variant | | |
SKCA-BR | 16 | 4429226 | 4429226 | single base substitution | C | T | intron_variant | | |
SKCA-BR | 16 | 4431738 | 4431738 | single base substitution | T | C | intron_variant | | |
SKCA-BR | 16 | 4432543 | 4432543 | single base substitution | A | C | intron_variant | | |
SKCA-BR | 16 | 4433178 | 4433178 | single base substitution | G | T | intron_variant | | |
SKCA-BR | 16 | 4434977 | 4434977 | insertion of <=200bp | - | CG | intron_variant | | |
SKCA-BR | 16 | 4435665 | 4435665 | single base substitution | C | T | intron_variant | | |
SKCA-BR | 16 | 4440739 | 4440739 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4441923 | 4441923 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4442296 | 4442296 | single base substitution | A | G | intron_variant | | |
SKCA-BR | 16 | 4443532 | 4443532 | single base substitution | G | T | intron_variant | | |
SKCA-BR | 16 | 4443660 | 4443660 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4447807 | 4447807 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4448203 | 4448203 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4449675 | 4449675 | single base substitution | G | T | intron_variant | | |
SKCA-BR | 16 | 4450300 | 4450300 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4453352 | 4453352 | single base substitution | G | C | intron_variant | | |
SKCA-BR | 16 | 4453414 | 4453414 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4457315 | 4457315 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4459105 | 4459105 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4463256 | 4463256 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4463947 | 4463947 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4466770 | 4466770 | single base substitution | G | A | 5_prime_UTR_variant | | |
SKCA-BR | 16 | 4466770 | 4466770 | single base substitution | G | A | upstream_gene_variant | | |
SKCA-BR | 16 | 4466771 | 4466771 | single base substitution | G | A | 5_prime_UTR_variant | | |
SKCA-BR | 16 | 4466771 | 4466771 | single base substitution | G | A | upstream_gene_variant | | |
SKCA-BR | 16 | 4468593 | 4468593 | single base substitution | T | G | intron_variant | | |
SKCA-BR | 16 | 4468593 | 4468593 | single base substitution | T | G | upstream_gene_variant | | |
SKCA-BR | 16 | 4468644 | 4468644 | single base substitution | G | A | intron_variant | | |
SKCA-BR | 16 | 4468644 | 4468644 | single base substitution | G | A | upstream_gene_variant | | |
SKCA-BR | 16 | 4473081 | 4473081 | single base substitution | C | A | upstream_gene_variant | | |
SKCA-BR | 16 | 4473114 | 4473114 | single base substitution | A | G | upstream_gene_variant | | |
SKCA-BR | 16 | 4473400 | 4473400 | single base substitution | T | A | upstream_gene_variant | | |
SKCM-US | 16 | 4386949 | 4386949 | single base substitution | A | C | downstream_gene_variant | | |
SKCM-US | 16 | 4393215 | 4393215 | single base substitution | C | G | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4393215 | 4393215 | single base substitution | C | G | intron_variant | | |
SKCM-US | 16 | 4393215 | 4393215 | single base substitution | C | G | missense_variant | E950D | 2850G>C |
SKCM-US | 16 | 4407228 | 4407228 | single base substitution | G | A | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4407228 | 4407228 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4407228 | 4407228 | single base substitution | G | A | missense_variant | R876W | 2626C>T |
SKCM-US | 16 | 4408059 | 4408059 | single base substitution | A | T | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4408059 | 4408059 | single base substitution | A | T | exon_variant | | |
SKCM-US | 16 | 4408059 | 4408059 | single base substitution | A | T | missense_variant | W835R | 2503T>A |
SKCM-US | 16 | 4408077 | 4408077 | single base substitution | G | A | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4408077 | 4408077 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4408077 | 4408077 | single base substitution | G | A | missense_variant | P829S | 2485C>T |
SKCM-US | 16 | 4409336 | 4409336 | single base substitution | G | A | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4409336 | 4409336 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4409336 | 4409336 | single base substitution | G | A | synonymous_variant | F767F | 2301C>T |
SKCM-US | 16 | 4409354 | 4409354 | single base substitution | G | A | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4409354 | 4409354 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4409354 | 4409354 | single base substitution | G | A | synonymous_variant | L761L | 2283C>T |
SKCM-US | 16 | 4411374 | 4411374 | single base substitution | G | A | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4411374 | 4411374 | single base substitution | G | A | missense_variant | R559C | 1675C>T |
SKCM-US | 16 | 4411374 | 4411374 | single base substitution | G | A | upstream_gene_variant | | |
SKCM-US | 16 | 4411379 | 4411379 | single base substitution | G | A | 3_prime_UTR_variant | | |
SKCM-US | 16 | 4411379 | 4411379 | single base substitution | G | A | missense_variant | P557L | 1670C>T |
SKCM-US | 16 | 4411379 | 4411379 | single base substitution | G | A | upstream_gene_variant | | |
SKCM-US | 16 | 4412714 | 4412714 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4412714 | 4412714 | single base substitution | G | A | missense_variant | S434L | 1301C>T |
SKCM-US | 16 | 4412714 | 4412714 | single base substitution | G | A | upstream_gene_variant | | |
SKCM-US | 16 | 4412724 | 4412724 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4412724 | 4412724 | single base substitution | G | A | missense_variant | P431S | 1291C>T |
SKCM-US | 16 | 4412724 | 4412724 | single base substitution | G | A | upstream_gene_variant | | |
SKCM-US | 16 | 4412725 | 4412725 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4412725 | 4412725 | single base substitution | G | A | synonymous_variant | S430S | 1290C>T |
SKCM-US | 16 | 4412725 | 4412725 | single base substitution | G | A | upstream_gene_variant | | |
SKCM-US | 16 | 4412726 | 4412726 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4412726 | 4412726 | single base substitution | G | A | missense_variant | S430F | 1289C>T |
SKCM-US | 16 | 4412726 | 4412726 | single base substitution | G | A | upstream_gene_variant | | |
SKCM-US | 16 | 4414375 | 4414375 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4414375 | 4414375 | single base substitution | G | A | missense_variant | P393S | 1177C>T |
SKCM-US | 16 | 4414791 | 4414791 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4414791 | 4414791 | single base substitution | G | A | synonymous_variant | Y343Y | 1029C>T |
SKCM-US | 16 | 4431025 | 4431025 | single base substitution | C | T | intron_variant | | |
SKCM-US | 16 | 4431310 | 4431310 | single base substitution | C | T | intron_variant | | |
SKCM-US | 16 | 4431686 | 4431686 | single base substitution | G | A | intron_variant | | |
SKCM-US | 16 | 4431850 | 4431850 | single base substitution | G | A | intron_variant | | |
SKCM-US | 16 | 4432028 | 4432028 | single base substitution | G | A | intron_variant | | |
SKCM-US | 16 | 4463325 | 4463325 | single base substitution | G | A | exon_variant | | |
SKCM-US | 16 | 4463325 | 4463325 | single base substitution | G | A | synonymous_variant | F47F | 141C>T |
STAD-US | 16 | 4386992 | 4386992 | single base substitution | G | A | downstream_gene_variant | | |
STAD-US | 16 | 4390324 | 4390324 | single base substitution | G | A | 3_prime_UTR_variant | | |
STAD-US | 16 | 4390324 | 4390324 | single base substitution | G | A | downstream_gene_variant | | |
STAD-US | 16 | 4390324 | 4390324 | single base substitution | G | A | missense_variant | T1048M | 3143C>T |
STAD-US | 16 | 4408008 | 4408008 | single base substitution | G | A | 3_prime_UTR_variant | | |
STAD-US | 16 | 4408008 | 4408008 | single base substitution | G | A | exon_variant | | |
STAD-US | 16 | 4408008 | 4408008 | single base substitution | G | A | missense_variant | P852S | 2554C>T |
STAD-US | 16 | 4409528 | 4409528 | single base substitution | G | T | 3_prime_UTR_variant | | |
STAD-US | 16 | 4409528 | 4409528 | single base substitution | G | T | missense_variant | L735M | 2203C>A |
STAD-US | 16 | 4409528 | 4409528 | single base substitution | G | T | upstream_gene_variant | | |
STAD-US | 16 | 4409546 | 4409546 | single base substitution | C | T | 3_prime_UTR_variant | | |
STAD-US | 16 | 4409546 | 4409546 | single base substitution | C | T | missense_variant | V729M | 2185G>A |
STAD-US | 16 | 4409546 | 4409546 | single base substitution | C | T | upstream_gene_variant | | |
STAD-US | 16 | 4409582 | 4409582 | single base substitution | G | T | 3_prime_UTR_variant | | |
STAD-US | 16 | 4409582 | 4409582 | single base substitution | G | T | missense_variant | L717M | 2149C>A |
STAD-US | 16 | 4409582 | 4409582 | single base substitution | G | T | upstream_gene_variant | | |
STAD-US | 16 | 4410338 | 4410338 | single base substitution | G | A | 3_prime_UTR_variant | | |
STAD-US | 16 | 4410338 | 4410338 | single base substitution | G | A | synonymous_variant | R683R | 2049C>T |
STAD-US | 16 | 4410338 | 4410338 | single base substitution | G | A | upstream_gene_variant | | |
STAD-US | 16 | 4411080 | 4411080 | single base substitution | G | A | 3_prime_UTR_variant | | |
STAD-US | 16 | 4411080 | 4411080 | single base substitution | G | A | missense_variant | T594M | 1781C>T |
STAD-US | 16 | 4411080 | 4411080 | single base substitution | G | A | upstream_gene_variant | | |
STAD-US | 16 | 4411442 | 4411442 | single base substitution | G | A | 3_prime_UTR_variant | | |
STAD-US | 16 | 4411442 | 4411442 | single base substitution | G | A | missense_variant | T536M | 1607C>T |
STAD-US | 16 | 4411442 | 4411442 | single base substitution | G | A | upstream_gene_variant | | |
STAD-US | 16 | 4412678 | 4412678 | single base substitution | G | T | exon_variant | | |
STAD-US | 16 | 4412678 | 4412678 | single base substitution | G | T | missense_variant | P446H | 1337C>A |
STAD-US | 16 | 4412678 | 4412678 | single base substitution | G | T | upstream_gene_variant | | |
STAD-US | 16 | 4415045 | 4415045 | single base substitution | T | C | exon_variant | | |
STAD-US | 16 | 4415045 | 4415045 | single base substitution | T | C | missense_variant | Y286C | 857A>G |
STAD-US | 16 | 4431585 | 4431585 | single base substitution | G | A | intron_variant | | |
STAD-US | 16 | 4431967 | 4431967 | single base substitution | C | T | intron_variant | | |
STAD-US | 16 | 4432050 | 4432050 | single base substitution | G | A | intron_variant | | |
STAD-US | 16 | 4432309 | 4432309 | single base substitution | C | T | intron_variant | | |
STAD-US | 16 | 4432529 | 4432529 | deletion of <=200bp | G | - | intron_variant | | |
STAD-US | 16 | 4438557 | 4438557 | single base substitution | C | T | exon_variant | | |
STAD-US | 16 | 4438557 | 4438557 | single base substitution | C | T | missense_variant | G231R | 691G>A |
STAD-US | 16 | 4457673 | 4457673 | single base substitution | G | A | exon_variant | | |
STAD-US | 16 | 4457673 | 4457673 | single base substitution | G | A | stop_gained | R106* | 316C>T |
STAD-US | 16 | 4463375 | 4463375 | single base substitution | C | T | exon_variant | | |
STAD-US | 16 | 4463375 | 4463375 | single base substitution | C | T | missense_variant | A31T | 91G>A |
THCA-SA | 16 | 4388139 | 4388139 | single base substitution | G | A | downstream_gene_variant | | |
THCA-SA | 16 | 4388441 | 4388441 | single base substitution | G | A | downstream_gene_variant | | |
THCA-SA | 16 | 4405018 | 4405018 | single base substitution | G | A | intron_variant | | |
THCA-SA | 16 | 4415055 | 4415055 | insertion of <=200bp | - | C | exon_variant | | |
THCA-SA | 16 | 4415055 | 4415055 | insertion of <=200bp | - | C | frameshift_variant | R283R? | |
THCA-US | 16 | 4411173 | 4411173 | single base substitution | A | C | 3_prime_UTR_variant | | |
THCA-US | 16 | 4411173 | 4411173 | single base substitution | A | C | synonymous_variant | T588T | 1764T>G |
THCA-US | 16 | 4411173 | 4411173 | single base substitution | A | C | upstream_gene_variant | | |
UCEC-US | 16 | 4390368 | 4390368 | single base substitution | T | G | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4390368 | 4390368 | single base substitution | T | G | downstream_gene_variant | | |
UCEC-US | 16 | 4390368 | 4390368 | single base substitution | T | G | missense_variant | K1033N | 3099A>C |
UCEC-US | 16 | 4393291 | 4393291 | single base substitution | G | A | intron_variant | | |
UCEC-US | 16 | 4393291 | 4393291 | single base substitution | G | A | missense_variant | A925V | 2774C>T |
UCEC-US | 16 | 4393291 | 4393291 | single base substitution | G | A | splice_region_variant | | |
UCEC-US | 16 | 4408026 | 4408026 | single base substitution | G | A | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4408026 | 4408026 | single base substitution | G | A | exon_variant | | |
UCEC-US | 16 | 4408026 | 4408026 | single base substitution | G | A | stop_gained | Q846* | 2536C>T |
UCEC-US | 16 | 4408101 | 4408101 | single base substitution | C | A | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4408101 | 4408101 | single base substitution | C | A | exon_variant | | |
UCEC-US | 16 | 4408101 | 4408101 | single base substitution | C | A | stop_gained | E821* | 2461G>T |
UCEC-US | 16 | 4408455 | 4408455 | single base substitution | G | A | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4408455 | 4408455 | single base substitution | G | A | exon_variant | | |
UCEC-US | 16 | 4408455 | 4408455 | single base substitution | G | A | synonymous_variant | C790C | 2370C>T |
UCEC-US | 16 | 4410510 | 4410510 | single base substitution | C | T | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4410510 | 4410510 | single base substitution | C | T | missense_variant | A653T | 1957G>A |
UCEC-US | 16 | 4410510 | 4410510 | single base substitution | C | T | upstream_gene_variant | | |
UCEC-US | 16 | 4410535 | 4410535 | single base substitution | G | T | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4410535 | 4410535 | single base substitution | G | T | synonymous_variant | A644A | 1932C>A |
UCEC-US | 16 | 4410535 | 4410535 | single base substitution | G | T | upstream_gene_variant | | |
UCEC-US | 16 | 4411019 | 4411019 | single base substitution | G | A | 3_prime_UTR_variant | | |
UCEC-US | 16 | 4411019 | 4411019 | single base substitution | G | A | synonymous_variant | S614S | 1842C>T |
UCEC-US | 16 | 4411019 | 4411019 | single base substitution | G | A | upstream_gene_variant | | |
UCEC-US | 16 | 4411087 | 4411087 | single base substitution | C | A | splice_acceptor_variant | | |
UCEC-US | 16 | 4411087 | 4411087 | single base substitution | C | A | upstream_gene_variant | | |
UCEC-US | 16 | 4412714 | 4412714 | single base substitution | G | A | exon_variant | | |
UCEC-US | 16 | 4412714 | 4412714 | single base substitution | G | A | missense_variant | S434L | 1301C>T |
UCEC-US | 16 | 4412714 | 4412714 | single base substitution | G | A | upstream_gene_variant | | |
UCEC-US | 16 | 4414870 | 4414870 | single base substitution | C | T | exon_variant | | |
UCEC-US | 16 | 4414870 | 4414870 | single base substitution | C | T | missense_variant | R317Q | 950G>A |
UCEC-US | 16 | 4432888 | 4432888 | single base substitution | G | A | intron_variant | | |
UCEC-US | 16 | 4458242 | 4458242 | single base substitution | G | A | exon_variant | | |
UCEC-US | 16 | 4458242 | 4458242 | single base substitution | G | A | synonymous_variant | T81T | 243C>T |