Item | Value |
---|---|
geneid | 1549 |
ensemblid | ENSG00000198077.11 |
hgncid | 2611 |
symbol | CYP2A7 |
name | cytochrome P450 family 2 subfamily A member 7 |
refseq_nuc | NM_000764.3 |
refseq_prot | NP_000755.2 |
ensembl_nuc | ENST00000301146.9 |
ensembl_prot | ENSP00000301146.4 |
mane_status | MANE Select |
chr | chr19 |
start | 40875439 |
end | 40882231 |
strand | - |
ver | v1.2 |
region | chr19:40875439-40882231 |
region5000 | chr19:40870439-40887231 |
regionname0 | CYP2A7_chr19_40875439_40882231 |
regionname5000 | CYP2A7_chr19_40870439_40887231 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 494 | 106 | 16 | 19 | 46 | 5 | 20 | 33 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0002 | 0/0 | 494 | 67 | 19 | 7 | 33 | 0 | 8 | 23 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0003 | 1/0 | 494 | 57 | 2 | 11 | 30 | 3 | 10 | 22 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0004 | 0/0 | 494 | 21 | 0 | 0 | 21 | 0 | 0 | 16 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0005 | 0/0 | 494 | 20 | 8 | 10 | 0 | 0 | 2 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0006 | 0/0 | 466 | 20 | 8 | 12 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(461): Show |
chr19 | 40870439 | 40887231 |
a0007 | 0/0 | 494 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0008 | 0/0 | 494 | 16 | 1 | 14 | 0 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0009 | 0/0 | 494 | 12 | 0 | 0 | 12 | 0 | 0 | 12 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0010 | 0/0 | 494 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0011 | 0/1 | 494 | 6 | 0 | 3 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0012 | 0/0 | 494 | 6 | 2 | 1 | 2 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0013 | 0/0 | 494 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0014 | 0/0 | 494 | 5 | 0 | 1 | 1 | 2 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0015 | 0/0 | 494 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0016 | 0/0 | 494 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0017 | 0/0 | 494 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0018 | 0/0 | 494 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0019 | 0/0 | 494 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0020 | 0/0 | 494 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0021 | 0/0 | 494 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0022 | 0/0 | 369 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(364): Show |
chr19 | 40870439 | 40887231 |
a0023 | 0/0 | 494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0024 | 0/0 | 494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0025 | 0/0 | 494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0026 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(461): Show |
chr19 | 40870439 | 40887231 |
a0027 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(461): Show |
chr19 | 40870439 | 40887231 |
a0028 | 0/0 | 100 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(95): Show |
chr19 | 40870439 | 40887231 |
a0029 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0030 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
a0031 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | MLASG others(489): Show |
chr19 | 40870439 | 40887231 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1482 | 104 | 16 | 19 | 44 | 5 | 20 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0001c0026 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0001c0030 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0002c0003 | 0/0 | 1482 | 51 | 3 | 7 | 33 | 0 | 8 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0002c0008 | 0/0 | 1482 | 13 | 13 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0002c0027 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0002c0035 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0002c0038 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0003c0002 | 1/0 | 1482 | 57 | 2 | 11 | 30 | 3 | 10 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0004c0004 | 0/0 | 1482 | 21 | 0 | 0 | 21 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0005c0005 | 0/0 | 1482 | 20 | 8 | 10 | 0 | 0 | 2 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0006c0010 | 0/0 | 1482 | 11 | 3 | 8 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0006c0016 | 0/0 | 1482 | 4 | 0 | 4 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0006c0021 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0006c0022 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0006c0028 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0007c0006 | 0/0 | 1482 | 19 | 18 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0008c0007 | 0/0 | 1482 | 16 | 1 | 14 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0009c0009 | 0/0 | 1482 | 12 | 0 | 0 | 12 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0010c0011 | 0/0 | 1482 | 8 | 8 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0010c0041 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0011c0012 | 0/1 | 1482 | 6 | 0 | 3 | 0 | 2 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0012c0014 | 0/0 | 1482 | 6 | 2 | 1 | 2 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0013c0013 | 0/0 | 1482 | 6 | 4 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0014c0015 | 0/0 | 1482 | 5 | 0 | 1 | 1 | 2 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0015c0018 | 0/0 | 1482 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0016c0020 | 0/0 | 1482 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0017c0019 | 0/0 | 1482 | 3 | 0 | 0 | 2 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0018c0017 | 0/0 | 1482 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0019c0025 | 0/0 | 1482 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0020c0024 | 0/0 | 1482 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0021c0023 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0022c0033 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0023c0036 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0024c0031 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0025c0039 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0026c0029 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0027c0040 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0028c0042 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0029c0037 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0030c0034 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 | ||
a0031c0032 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATGCT others(1477): Show |
chr19 | 40870439 | 40887231 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1760 | 24 | 15 | 3 | 4 | 0 | 2 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0001c0001t0002 | 0/0 | 1760 | 69 | 1 | 11 | 37 | 4 | 16 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0001c0001t0003 | 0/0 | 1760 | 3 | 0 | 2 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0001c0001t0005 | 0/0 | 1760 | 4 | 0 | 0 | 2 | 0 | 2 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0001c0001t0006 | 0/0 | 1760 | 4 | 0 | 3 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0001c0026t0002 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0001c0030t0004 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0003t0001 | 0/0 | 1760 | 47 | 3 | 6 | 32 | 0 | 6 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0003t0002 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0003t0003 | 0/0 | 1760 | 2 | 0 | 0 | 1 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0003t0004 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0008t0001 | 0/0 | 1760 | 12 | 12 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0008t0005 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0027t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0035t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0002c0038t0007 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0002 | 0/0 | 1760 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0003 | 1/0 | 1760 | 35 | 0 | 10 | 12 | 3 | 9 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0004 | 0/0 | 1760 | 11 | 0 | 1 | 10 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0005 | 0/0 | 1760 | 5 | 0 | 0 | 5 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0006 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0008 | 0/0 | 1760 | 2 | 1 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0003c0002t0009 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0004c0004t0003 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0004c0004t0004 | 0/0 | 1760 | 13 | 0 | 0 | 13 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0004c0004t0005 | 0/0 | 1760 | 7 | 0 | 0 | 7 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0005c0005t0001 | 0/0 | 1760 | 17 | 7 | 9 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0005c0005t0002 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0005c0005t0004 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0005c0005t0007 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0006c0010t0001 | 0/0 | 1760 | 11 | 3 | 8 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0006c0016t0001 | 0/0 | 1760 | 4 | 0 | 4 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0006c0021t0007 | 0/0 | 1760 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0006c0022t0002 | 0/0 | 1760 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0006c0028t0007 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0007c0006t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0007c0006t0002 | 0/0 | 1760 | 15 | 15 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0007c0006t0004 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0007c0006t0011 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0007c0006t0012 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0008c0007t0003 | 0/0 | 1760 | 15 | 0 | 14 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0008c0007t0009 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0009c0009t0001 | 0/0 | 1760 | 9 | 0 | 0 | 9 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0009c0009t0004 | 0/0 | 1760 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0009c0009t0013 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0010c0011t0001 | 0/0 | 1760 | 8 | 8 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0010c0041t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0011c0012t0001 | 0/1 | 1760 | 6 | 0 | 3 | 0 | 2 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0012c0014t0001 | 0/0 | 1760 | 4 | 2 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0012c0014t0002 | 0/0 | 1760 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0013c0013t0001 | 0/0 | 1760 | 6 | 4 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0014c0015t0001 | 0/0 | 1760 | 2 | 0 | 0 | 1 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0014c0015t0003 | 0/0 | 1760 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0014c0015t0005 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0015c0018t0001 | 0/0 | 1760 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0016c0020t0001 | 0/0 | 1760 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0017c0019t0002 | 0/0 | 1760 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0017c0019t0003 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0018c0017t0001 | 0/0 | 1760 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0019c0025t0010 | 0/0 | 1760 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0020c0024t0005 | 0/0 | 1760 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0021c0023t0001 | 0/0 | 1760 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0022c0033t0002 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0023c0036t0004 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0024c0031t0003 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0025c0039t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0026c0029t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0027c0040t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0028c0042t0001 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0029c0037t0001 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0030c0034t0001 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
a0031c0032t0001 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | ATCTG others(1755): Show |
chr19 | 40870439 | 40887231 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 21 | 13 | 3 | 4 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0001 | 0/0 | 57 | 1 | 10 | 31 | 3 | 12 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0005g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0006g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0026t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0001c0030t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0002 | 0/0 | 37 | 3 | 6 | 22 | 0 | 6 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0008t0001g0008 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0008t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0008t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0027t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0035t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0002c0038t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0010 | 1/0 | 6 | 0 | 0 | 3 | 1 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0014 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0026 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0003c0002t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0004c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0004c0004t0004g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0004c0004t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0004c0004t0005g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0004c0004t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0004c0004t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0005c0005t0001g0006 | 0/0 | 12 | 4 | 8 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0005c0005t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0005c0005t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0005c0005t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0005c0005t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0005c0005t0007g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0006c0010t0001g0007 | 0/0 | 11 | 3 | 8 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0006c0016t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0006c0021t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0006c0021t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0006c0022t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0006c0028t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0007c0006t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0008c0007t0003g0004 | 0/0 | 15 | 0 | 14 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0008c0007t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0009c0009t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0009c0009t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0009c0009t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0009c0009t0013g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0011t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0010c0041t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0011c0012t0001g0011 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0011c0012t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0012c0014t0001g0013 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0012c0014t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0012c0014t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0013c0013t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0013c0013t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0013c0013t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0013c0013t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0013c0013t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0013c0013t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0014c0015t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0014c0015t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0014c0015t0003g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0014c0015t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0015c0018t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0015c0018t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0015c0018t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0016c0020t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0017c0019t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0017c0019t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0017c0019t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0018c0017t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0019c0025t0010g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0019c0025t0010g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0020c0024t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0020c0024t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0021c0023t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0021c0023t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0022c0033t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0023c0036t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0024c0031t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0025c0039t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0026c0029t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0027c0040t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0028c0042t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0029c0037t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0030c0034t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
a0031c0032t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0002 | t0003 | g0010 | EUR | GBR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00140 | hp1 | a0011 | c0012 | t0001 | g0011 | EUR | GBR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | GBR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00323 | hp2 | a0014 | c0015 | t0005 | g0124 | EUR | FIN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00408 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00423 | hp1 | a0015 | c0018 | t0001 | g0060 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00544 | hp2 | a0012 | c0014 | t0002 | g0093 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00597 | hp1 | a0015 | c0018 | t0001 | g0079 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00609 | hp1 | a0003 | c0002 | t0004 | g0156 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00609 | hp2 | a0014 | c0015 | t0001 | g0121 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00621 | hp1 | a0003 | c0002 | t0004 | g0149 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00639 | hp2 | a0007 | c0006 | t0004 | g0088 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00642 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00642 | hp2 | a0005 | c0005 | t0001 | g0006 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00673 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00733 | hp2 | a0014 | c0015 | t0003 | g0034 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00735 | hp2 | a0003 | c0002 | t0003 | g0014 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00738 | hp1 | a0006 | c0010 | t0001 | g0007 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00738 | hp2 | a0005 | c0005 | t0001 | g0006 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00741 | hp1 | a0003 | c0002 | t0003 | g0151 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG00741 | hp2 | a0005 | c0005 | t0001 | g0033 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01069 | hp2 | a0022 | c0033 | t0002 | g0067 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01070 | hp1 | a0006 | c0010 | t0001 | g0007 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01071 | hp2 | a0006 | c0010 | t0001 | g0007 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01081 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01081 | hp2 | a0005 | c0005 | t0002 | g0097 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01099 | hp1 | a0003 | c0002 | t0003 | g0039 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01099 | hp2 | a0006 | c0010 | t0001 | g0007 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01106 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01106 | hp2 | a0003 | c0002 | t0003 | g0039 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01167 | hp2 | a0008 | c0007 | t0003 | g0004 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01168 | hp2 | a0006 | c0016 | t0001 | g0015 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01169 | hp1 | a0006 | c0016 | t0001 | g0015 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01169 | hp2 | a0008 | c0007 | t0003 | g0004 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01175 | hp1 | a0006 | c0010 | t0001 | g0007 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01175 | hp2 | a0005 | c0005 | t0001 | g0006 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01192 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01243 | hp2 | a0019 | c0025 | t0010 | g0086 | AMR | PUR | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01255 | hp1 | a0006 | c0010 | t0001 | g0007 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01255 | hp2 | a0005 | c0005 | t0001 | g0006 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01256 | hp1 | a0006 | c0016 | t0001 | g0015 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01256 | hp2 | a0011 | c0012 | t0001 | g0011 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01257 | hp1 | a0012 | c0014 | t0001 | g0013 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01257 | hp2 | a0006 | c0010 | t0001 | g0007 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01258 | hp1 | a0011 | c0012 | t0001 | g0011 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01258 | hp2 | a0006 | c0010 | t0001 | g0007 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01261 | hp1 | a0011 | c0012 | t0001 | g0011 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01346 | hp2 | a0003 | c0002 | t0003 | g0040 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01358 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01361 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01433 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01496 | hp1 | a0013 | c0013 | t0001 | g0116 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01496 | hp2 | a0003 | c0002 | t0003 | g0026 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01516 | hp1 | a0003 | c0002 | t0003 | g0137 | EUR | IBS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0019 | EUR | IBS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01517 | hp1 | a0003 | c0002 | t0003 | g0038 | EUR | IBS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01517 | hp2 | a0011 | c0012 | t0001 | g0011 | EUR | IBS | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01884 | hp1 | a0013 | c0013 | t0001 | g0087 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01891 | hp1 | a0006 | c0022 | t0002 | g0028 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01928 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01928 | hp2 | a0019 | c0025 | t0010 | g0085 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0072 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01934 | hp2 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01943 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01952 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01975 | hp2 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01978 | hp1 | a0003 | c0002 | t0003 | g0014 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01978 | hp2 | a0003 | c0002 | t0003 | g0037 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01981 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01981 | hp2 | a0006 | c0016 | t0001 | g0015 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01993 | hp1 | a0003 | c0002 | t0003 | g0038 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01993 | hp2 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02004 | hp1 | a0003 | c0002 | t0004 | g0162 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02004 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02015 | hp1 | a0003 | c0002 | t0003 | g0132 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02015 | hp2 | a0015 | c0018 | t0001 | g0053 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02027 | hp1 | a0003 | c0002 | t0003 | g0135 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02040 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02055 | hp1 | a0010 | c0011 | t0001 | g0102 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02055 | hp2 | a0002 | c0008 | t0001 | g0045 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02056 | hp2 | a0020 | c0024 | t0005 | g0155 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02074 | hp1 | a0002 | c0003 | t0001 | g0074 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02074 | hp2 | a0001 | c0030 | t0004 | g0062 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02080 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02083 | hp1 | a0003 | c0002 | t0003 | g0010 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02083 | hp2 | a0020 | c0024 | t0005 | g0146 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02129 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02129 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02135 | hp1 | a0012 | c0014 | t0002 | g0094 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02145 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02148 | hp1 | a0023 | c0036 | t0004 | g0058 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02148 | hp2 | a0002 | c0003 | t0002 | g0057 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02155 | hp1 | a0003 | c0002 | t0003 | g0010 | EAS | CDX | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02155 | hp2 | a0003 | c0002 | t0003 | g0112 | EAS | CDX | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02165 | hp2 | a0003 | c0002 | t0005 | g0130 | EAS | CDX | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02257 | hp2 | a0013 | c0013 | t0001 | g0118 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02258 | hp1 | a0007 | c0006 | t0002 | g0022 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02258 | hp2 | a0013 | c0013 | t0001 | g0113 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02273 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02273 | hp2 | a0024 | c0031 | t0003 | g0063 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02280 | hp2 | a0007 | c0006 | t0002 | g0024 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02293 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02293 | hp2 | a0003 | c0002 | t0003 | g0037 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02300 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02300 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02451 | hp1 | a0007 | c0006 | t0011 | g0105 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02451 | hp2 | a0010 | c0011 | t0001 | g0103 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02602 | hp1 | a0002 | c0003 | t0003 | g0055 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02602 | hp2 | a0003 | c0002 | t0003 | g0147 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02615 | hp1 | a0013 | c0013 | t0001 | g0115 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02615 | hp2 | a0027 | c0040 | t0001 | g0101 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02622 | hp1 | a0005 | c0005 | t0004 | g0096 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02622 | hp2 | a0005 | c0005 | t0001 | g0021 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02630 | hp1 | a0002 | c0008 | t0001 | g0008 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02630 | hp2 | a0007 | c0006 | t0012 | g0108 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02647 | hp1 | a0002 | c0027 | t0001 | g0046 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02647 | hp2 | a0007 | c0006 | t0002 | g0023 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02683 | hp1 | a0003 | c0002 | t0003 | g0014 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02717 | hp1 | a0002 | c0008 | t0001 | g0008 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02717 | hp2 | a0007 | c0006 | t0002 | g0106 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02723 | hp1 | a0012 | c0014 | t0001 | g0013 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02723 | hp2 | a0002 | c0035 | t0001 | g0165 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02735 | hp1 | a0014 | c0015 | t0003 | g0034 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02735 | hp2 | a0017 | c0019 | t0003 | g0143 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02738 | hp2 | a0003 | c0002 | t0006 | g0134 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02809 | hp1 | a0002 | c0008 | t0001 | g0008 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02809 | hp2 | a0016 | c0020 | t0001 | g0025 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02818 | hp1 | a0012 | c0014 | t0001 | g0013 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02818 | hp2 | a0002 | c0008 | t0001 | g0008 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02886 | hp1 | a0007 | c0006 | t0001 | g0110 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02895 | hp1 | a0007 | c0006 | t0002 | g0023 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02897 | hp1 | a0007 | c0006 | t0002 | g0023 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02897 | hp2 | a0006 | c0021 | t0007 | g0164 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02922 | hp1 | a0007 | c0006 | t0002 | g0104 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02922 | hp2 | a0002 | c0008 | t0001 | g0008 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02965 | hp1 | a0002 | c0008 | t0001 | g0008 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02965 | hp2 | a0007 | c0006 | t0002 | g0024 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02970 | hp1 | a0006 | c0022 | t0002 | g0028 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02970 | hp2 | a0008 | c0007 | t0009 | g0070 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02976 | hp1 | a0002 | c0008 | t0001 | g0008 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02976 | hp2 | a0010 | c0041 | t0001 | g0120 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03017 | hp2 | a0005 | c0005 | t0007 | g0095 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03041 | hp1 | a0010 | c0011 | t0001 | g0125 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03041 | hp2 | a0002 | c0008 | t0001 | g0008 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03098 | hp1 | a0003 | c0002 | t0009 | g0144 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03130 | hp1 | a0007 | c0006 | t0002 | g0024 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03130 | hp2 | a0002 | c0008 | t0001 | g0008 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03139 | hp2 | a0007 | c0006 | t0002 | g0117 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03195 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03209 | hp1 | a0007 | c0006 | t0002 | g0109 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03209 | hp2 | a0007 | c0006 | t0002 | g0107 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03225 | hp1 | a0005 | c0005 | t0001 | g0021 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03225 | hp2 | a0002 | c0008 | t0001 | g0047 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03239 | hp2 | a0003 | c0002 | t0003 | g0014 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03453 | hp1 | a0007 | c0006 | t0002 | g0022 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03453 | hp2 | a0006 | c0021 | t0007 | g0163 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03486 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03486 | hp2 | a0010 | c0011 | t0001 | g0035 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | ESN | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03540 | hp1 | a0003 | c0002 | t0008 | g0148 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03579 | hp2 | a0010 | c0011 | t0001 | g0122 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03669 | hp1 | a0005 | c0005 | t0001 | g0033 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03669 | hp2 | a0003 | c0002 | t0003 | g0026 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03704 | hp1 | a0003 | c0002 | t0003 | g0141 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03704 | hp2 | a0012 | c0014 | t0001 | g0013 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03834 | hp1 | a0003 | c0002 | t0003 | g0040 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0020 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03927 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03942 | hp2 | a0003 | c0002 | t0003 | g0145 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04115 | hp1 | a0003 | c0002 | t0003 | g0010 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04184 | hp2 | a0003 | c0002 | t0003 | g0026 | SAS | BEB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0066 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04204 | hp1 | a0008 | c0007 | t0003 | g0004 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04204 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18522 | hp1 | a0006 | c0028 | t0007 | g0044 | AFR | YRI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18522 | hp2 | a0028 | c0042 | t0001 | g0127 | AFR | YRI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18612 | hp1 | a0002 | c0003 | t0003 | g0061 | EAS | CHB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18612 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CHB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18906 | hp1 | a0006 | c0010 | t0001 | g0007 | AFR | YRI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18906 | hp2 | a0005 | c0005 | t0001 | g0006 | AFR | YRI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18939 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18941 | hp1 | a0003 | c0002 | t0004 | g0160 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18941 | hp2 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18943 | hp1 | a0001 | c0026 | t0002 | g0052 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18946 | hp2 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18947 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18948 | hp1 | a0004 | c0004 | t0005 | g0012 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18948 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18950 | hp1 | a0003 | c0002 | t0002 | g0150 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18950 | hp2 | a0017 | c0019 | t0002 | g0133 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18951 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18953 | hp1 | a0004 | c0004 | t0004 | g0099 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18953 | hp2 | a0003 | c0002 | t0004 | g0036 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18957 | hp1 | a0004 | c0004 | t0005 | g0012 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18957 | hp2 | a0003 | c0002 | t0003 | g0027 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18964 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18967 | hp1 | a0003 | c0002 | t0003 | g0027 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18968 | hp1 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18970 | hp1 | a0003 | c0002 | t0003 | g0142 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18970 | hp2 | a0003 | c0002 | t0005 | g0153 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18971 | hp2 | a0003 | c0002 | t0005 | g0128 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18977 | hp1 | a0009 | c0009 | t0001 | g0041 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18977 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18980 | hp1 | a0029 | c0037 | t0001 | g0059 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18980 | hp2 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18982 | hp2 | a0017 | c0019 | t0002 | g0136 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18983 | hp1 | a0003 | c0002 | t0003 | g0027 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18983 | hp2 | a0003 | c0002 | t0003 | g0140 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18984 | hp1 | a0009 | c0009 | t0013 | g0092 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18984 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18988 | hp2 | a0030 | c0034 | t0001 | g0068 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18989 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18993 | hp1 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18995 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19000 | hp1 | a0004 | c0004 | t0005 | g0100 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19000 | hp2 | a0004 | c0004 | t0003 | g0098 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19001 | hp1 | a0004 | c0004 | t0005 | g0089 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19001 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19003 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19004 | hp1 | a0003 | c0002 | t0008 | g0154 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19004 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19005 | hp2 | a0003 | c0002 | t0003 | g0158 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19010 | hp2 | a0004 | c0004 | t0005 | g0012 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19011 | hp1 | a0003 | c0002 | t0002 | g0152 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19011 | hp2 | a0009 | c0009 | t0004 | g0032 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19012 | hp1 | a0003 | c0002 | t0004 | g0161 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19030 | hp1 | a0010 | c0011 | t0001 | g0119 | AFR | LWK | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19043 | hp2 | a0002 | c0008 | t0005 | g0042 | AFR | LWK | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19054 | hp1 | a0018 | c0017 | t0001 | g0017 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19055 | hp2 | a0003 | c0002 | t0004 | g0131 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19056 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19056 | hp2 | a0003 | c0002 | t0004 | g0157 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19058 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19059 | hp1 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19059 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19060 | hp1 | a0003 | c0002 | t0003 | g0010 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19060 | hp2 | a0004 | c0004 | t0005 | g0012 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19065 | hp1 | a0003 | c0002 | t0004 | g0159 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19066 | hp1 | a0009 | c0009 | t0004 | g0032 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19067 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19068 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19070 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19070 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19072 | hp2 | a0018 | c0017 | t0001 | g0017 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19077 | hp1 | a0031 | c0032 | t0001 | g0082 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19077 | hp2 | a0003 | c0002 | t0005 | g0129 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19079 | hp1 | a0003 | c0002 | t0004 | g0139 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19079 | hp2 | a0003 | c0002 | t0005 | g0138 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19080 | hp2 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19085 | hp2 | a0009 | c0009 | t0001 | g0009 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19086 | hp1 | a0018 | c0017 | t0001 | g0017 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19086 | hp2 | a0004 | c0004 | t0005 | g0012 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19240 | hp1 | a0007 | c0006 | t0002 | g0111 | AFR | YRI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA19240 | hp2 | a0021 | c0023 | t0001 | g0090 | AFR | YRI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20129 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | ASW | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20129 | hp2 | a0006 | c0010 | t0001 | g0007 | AFR | ASW | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20752 | hp1 | a0014 | c0015 | t0001 | g0123 | EUR | TSI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20905 | hp2 | a0002 | c0003 | t0004 | g0056 | SAS | GIH | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01123 | hp1 | a0008 | c0007 | t0003 | g0004 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG01123 | hp2 | a0013 | c0013 | t0001 | g0114 | AMR | CLM | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02109 | hp1 | a0007 | c0006 | t0002 | g0022 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02109 | hp2 | a0016 | c0020 | t0001 | g0025 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02486 | hp1 | a0025 | c0039 | t0001 | g0084 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02486 | hp2 | a0026 | c0029 | t0001 | g0043 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG02559 | hp2 | a0005 | c0005 | t0001 | g0021 | AFR | ACB | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03471 | hp1 | a0010 | c0011 | t0001 | g0035 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG03471 | hp2 | a0016 | c0020 | t0001 | g0025 | AFR | MSL | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG06807 | hp1 | a0002 | c0008 | t0001 | g0008 | AFR | USA | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA18955 | hp2 | a0003 | c0002 | t0004 | g0036 | EAS | JPT | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20300 | hp1 | a0002 | c0038 | t0007 | g0048 | AFR | USA | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA20300 | hp2 | a0006 | c0010 | t0001 | g0007 | AFR | USA | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA21309 | hp1 | a0010 | c0011 | t0001 | g0126 | AFR | LWK | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
NA21309 | hp2 | a0021 | c0023 | t0001 | g0091 | AFR | LWK | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
homoSapiens | chm13v2 | a0011 | c0012 | t0001 | g0050 | REF | REF | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
homoSapiens | grch38p0 | a0003 | c0002 | t0003 | g0010 | REF | REF | CYP2A7_chr19_40870439_40887231 | CYP2A7 | chr19 | 40870439 | 40887231 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40875709 | C | T | 1 | a0020 | 2 | HG02056.hp2 HG02083.hp2 |
missense_variant | MODERATE | c.1469G>A | p.Ser490Asn | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 1490/1760 | 1469/1485 | 490/494 | chr19 | 40875709 | |||
chr19:40875742 | A | C | 24 | a0001 a0002 a0004 others(21): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
missense_variant | MODERATE | c.1436T>G | p.Val479Gly | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 1457/1760 | 1436/1485 | 479/494 | chr19 | 40875742 | |||
chr19:40875778 | G | T | 3 | a0006 a0026 a0027 |
22 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
stop_gained | HIGH | c.1400C>A | p.Ser467* | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 1421/1760 | 1400/1485 | 467/494 | chr19 | 40875778 | |||
chr19:40875866 | T | A | 3 | a0004 a0005 a0028 |
42 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(39): Show |
missense_variant | MODERATE | c.1312A>T | p.Asn438Tyr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 1333/1760 | 1312/1485 | 438/494 | chr19 | 40875866 | |||
chr19:40876571 | T | A | 2 | a0010 a0014 |
14 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(11): Show |
missense_variant | MODERATE | c.1259A>T | p.Lys420Met | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1280/1760 | 1259/1485 | 420/494 | chr19 | 40876571 | |||
chr19:40876573 | G | C | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.1257C>G | p.Asp419Glu | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1278/1760 | 1257/1485 | 419/494 | chr19 | 40876573 | |||
chr19:40876578 | C | T | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.1252G>A | p.Asp418Asn | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1273/1760 | 1252/1485 | 418/494 | chr19 | 40876578 | |||
chr19:40876655 | A | T | 2 | a0014 a0019 |
7 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(4): Show |
missense_variant | MODERATE | c.1175T>A | p.Phe392Tyr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1196/1760 | 1175/1485 | 392/494 | chr19 | 40876655 | |||
chr19:40876662 | C | T | 1 | a0030 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.1168G>A | p.Glu390Lys | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1189/1760 | 1168/1485 | 390/494 | chr19 | 40876662 | |||
chr19:40877200 | A | G | 1 | a0029 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.1151T>C | p.Phe384Ser | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1172/1760 | 1151/1485 | 384/494 | chr19 | 40877200 | |||
chr19:40877236 | C | T | 1 | a0021 | 2 | NA19240.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.1115G>A | p.Arg372His | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1136/1760 | 1115/1485 | 372/494 | chr19 | 40877236 | |||
chr19:40877242 | A | T | 1 | a0022 | 1 | HG01069.hp2 | stop_gained | HIGH | c.1109T>A | p.Leu370* | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1130/1760 | 1109/1485 | 370/494 | chr19 | 40877242 | |||
chr19:40877248 | A | G | 5 | a0001 a0008 a0022 others(2): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
missense_variant | MODERATE | c.1103T>C | p.Met368Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1124/1760 | 1103/1485 | 368/494 | chr19 | 40877248 | |||
chr19:40877269 | C | A | 1 | a0029 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.1082G>T | p.Arg361Ile | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1103/1760 | 1082/1485 | 361/494 | chr19 | 40877269 | |||
chr19:40877312 | T | C | 11 | a0004 a0005 a0009 others(8): Show |
83 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(80): Show |
missense_variant | MODERATE | c.1039A>G | p.Thr347Ala | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1060/1760 | 1039/1485 | 347/494 | chr19 | 40877312 | |||
chr19:40877315 | G | A | 1 | a0026 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1036C>T | p.Arg346Trp | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1057/1760 | 1036/1485 | 346/494 | chr19 | 40877315 | |||
chr19:40877335 | C | G | 1 | a0031 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.1016G>C | p.Arg339Pro | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1037/1760 | 1016/1485 | 339/494 | chr19 | 40877335 | |||
chr19:40877359 | A | G | 1 | a0027 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.992T>C | p.Ile331Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1013/1760 | 992/1485 | 331/494 | chr19 | 40877359 | |||
chr19:40877894 | G | A | 14 | a0001 a0002 a0006 others(11): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
missense_variant | MODERATE | c.931C>T | p.Arg311Cys | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 952/1760 | 931/1485 | 311/494 | chr19 | 40877894 | |||
chr19:40877923 | G | C | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.902C>G | p.Ala301Gly | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 923/1760 | 902/1485 | 301/494 | chr19 | 40877923 | |||
chr19:40877944 | C | G | 2 | a0011 a0019 |
7 | HG00140.hp1 HG01243.hp2 HG01256.hp2 others(4): Show |
missense_variant | MODERATE | c.881G>C | p.Ser294Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 902/1760 | 881/1485 | 294/494 | chr19 | 40877944 | |||
chr19:40877951 | T | C | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.874A>G | p.Met292Val | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 895/1760 | 874/1485 | 292/494 | chr19 | 40877951 | |||
chr19:40878770 | T | C | 28 | a0001 a0002 a0004 others(25): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
missense_variant | MODERATE | c.821A>G | p.His274Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 842/1760 | 821/1485 | 274/494 | chr19 | 40878770 | |||
chr19:40878797 | T | C | 6 | a0005 a0010 a0012 others(3): Show |
43 | HG00323.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
missense_variant | MODERATE | c.794A>G | p.Gln265Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 815/1760 | 794/1485 | 265/494 | chr19 | 40878797 | |||
chr19:40878876 | T | G | 5 | a0010 a0013 a0014 others(2): Show |
23 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(20): Show |
missense_variant | MODERATE | c.715A>C | p.Lys239Gln | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 736/1760 | 715/1485 | 239/494 | chr19 | 40878876 | |||
chr19:40878881 | G | C | 1 | a0015 | 3 | HG00423.hp1 HG00597.hp1 HG02015.hp2 |
missense_variant | MODERATE | c.710C>G | p.Ala237Gly | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 731/1760 | 710/1485 | 237/494 | chr19 | 40878881 | |||
chr19:40880128 | T | C | 5 | a0004 a0005 a0009 others(2): Show |
60 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
missense_variant | MODERATE | c.610A>G | p.Met204Val | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/9 | 631/1760 | 610/1485 | 204/494 | chr19 | 40880128 | |||
chr19:40880131 | T | G | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.607A>C | p.Ser203Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/9 | 628/1760 | 607/1485 | 203/494 | chr19 | 40880131 | |||
chr19:40880158 | C | T | 2 | a0019 a0024 |
3 | HG01243.hp2 HG01928.hp2 HG02273.hp2 |
missense_variant | MODERATE | c.580G>A | p.Glu194Lys | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/9 | 601/1760 | 580/1485 | 194/494 | chr19 | 40880158 | |||
chr19:40880231 | A | C | 14 | a0001 a0002 a0006 others(11): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
missense_variant | MODERATE | c.507T>G | p.Asp169Glu | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/9 | 528/1760 | 507/1485 | 169/494 | chr19 | 40880231 | |||
chr19:40880481 | T | C | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant&splice_region_variant | MODERATE | c.491A>G | p.His164Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 512/1760 | 491/1485 | 164/494 | chr19 | 40880481 | |||
chr19:40880482 | G | C | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.490C>G | p.His164Asp | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 511/1760 | 490/1485 | 164/494 | chr19 | 40880482 | |||
chr19:40880488 | T | C | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.484A>G | p.Ser162Gly | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 505/1760 | 484/1485 | 162/494 | chr19 | 40880488 | |||
chr19:40880494 | T | G | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.478A>C | p.Ile160Leu | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 499/1760 | 478/1485 | 160/494 | chr19 | 40880494 | |||
chr19:40880498 | C | G | 1 | a0019 | 2 | HG01243.hp2 HG01928.hp2 |
missense_variant | MODERATE | c.474G>C | p.Glu158Asp | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 495/1760 | 474/1485 | 158/494 | chr19 | 40880498 | |||
chr19:40880515 | A | C | 15 | a0001 a0002 a0006 others(12): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
missense_variant | MODERATE | c.457T>G | p.Ser153Ala | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 478/1760 | 457/1485 | 153/494 | chr19 | 40880515 | |||
chr19:40880575 | C | G | 1 | a0021 | 2 | NA19240.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.397G>C | p.Ala133Pro | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 418/1760 | 397/1485 | 133/494 | chr19 | 40880575 | |||
chr19:40880581 | C | A | 15 | a0001 a0002 a0006 others(12): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
missense_variant | MODERATE | c.391G>T | p.Ala131Ser | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 412/1760 | 391/1485 | 131/494 | chr19 | 40880581 | |||
chr19:40880589 | A | C | 15 | a0001 a0002 a0006 others(12): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
missense_variant | MODERATE | c.383T>G | p.Leu128Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 404/1760 | 383/1485 | 128/494 | chr19 | 40880589 | |||
chr19:40880622 | G | A | 15 | a0001 a0002 a0006 others(12): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
missense_variant | MODERATE | c.350C>T | p.Ala117Val | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 371/1760 | 350/1485 | 117/494 | chr19 | 40880622 | |||
chr19:40881631 | G | A | 1 | a0028 | 1 | NA18522.hp2 | stop_gained | HIGH | c.301C>T | p.Arg101* | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/9 | 322/1760 | 301/1485 | 101/494 | chr19 | 40881631 | |||
chr19:40881742 | A | G | 15 | a0001 a0002 a0006 others(12): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
missense_variant | MODERATE | c.190T>C | p.Cys64Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/9 | 211/1760 | 190/1485 | 64/494 | chr19 | 40881742 | |||
chr19:40881751 | A | T | 14 | a0001 a0002 a0006 others(11): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
missense_variant&splice_region_variant | MODERATE | c.181T>A | p.Phe61Ile | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/9 | 202/1760 | 181/1485 | 61/494 | chr19 | 40881751 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40875738 | A | G | 1 | a0002c0038 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1440T>C | p.Phe480Phe | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 1461/1760 | 1440/1485 | 480/494 | chr19 | 40875738 | |||
chr19:40876585 | A | G | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.1245T>C | p.His415His | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1266/1760 | 1245/1485 | 415/494 | chr19 | 40876585 | |||
chr19:40876606 | A | G | 1 | a0006c0028 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1224T>C | p.Pro408Pro | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1245/1760 | 1224/1485 | 408/494 | chr19 | 40876606 | |||
chr19:40876621 | G | A | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.1209C>T | p.Ser403Ser | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1230/1760 | 1209/1485 | 403/494 | chr19 | 40876621 | |||
chr19:40876639 | G | A | 3 | a0006c0022 a0006c0028 a0019c0025 |
5 | HG01243.hp2 HG01891.hp1 HG01928.hp2 others(2): Show |
synonymous_variant | LOW | c.1191C>T | p.Ser397Ser | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/9 | 1212/1760 | 1191/1485 | 397/494 | chr19 | 40876639 | |||
chr19:40877202 | A | G | 2 | a0018c0017 a0019c0025 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
synonymous_variant | LOW | c.1149T>C | p.Phe383Phe | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1170/1760 | 1149/1485 | 383/494 | chr19 | 40877202 | |||
chr19:40877229 | A | G | 2 | a0018c0017 a0019c0025 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
synonymous_variant | LOW | c.1122T>C | p.Val374Val | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1143/1760 | 1122/1485 | 374/494 | chr19 | 40877229 | |||
chr19:40877232 | C | T | 2 | a0018c0017 a0019c0025 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
synonymous_variant | LOW | c.1119G>A | p.Arg373Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1140/1760 | 1119/1485 | 373/494 | chr19 | 40877232 | |||
chr19:40877259 | G | A | 1 | a0002c0035 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1092C>T | p.Asp364Asp | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1113/1760 | 1092/1485 | 364/494 | chr19 | 40877259 | |||
chr19:40877310 | G | C | 6 | a0002c0003 a0011c0012 a0015c0018 others(3): Show |
62 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
synonymous_variant | LOW | c.1041C>G | p.Thr347Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/9 | 1062/1760 | 1041/1485 | 347/494 | chr19 | 40877310 | |||
chr19:40877910 | C | G | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.915G>C | p.Thr305Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 936/1760 | 915/1485 | 305/494 | chr19 | 40877910 | |||
chr19:40877916 | G | A | 1 | a0027c0040 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.909C>T | p.Thr303Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 930/1760 | 909/1485 | 303/494 | chr19 | 40877916 | |||
chr19:40877922 | T | C | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.903A>G | p.Ala301Ala | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 924/1760 | 903/1485 | 301/494 | chr19 | 40877922 | |||
chr19:40877958 | C | T | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.867G>A | p.Lys289Lys | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/9 | 888/1760 | 867/1485 | 289/494 | chr19 | 40877958 | |||
chr19:40878763 | C | T | 1 | a0010c0041 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.828G>A | p.Gln276Gln | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 849/1760 | 828/1485 | 276/494 | chr19 | 40878763 | |||
chr19:40878787 | G | A | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.804C>T | p.Ile268Ile | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 825/1760 | 804/1485 | 268/494 | chr19 | 40878787 | |||
chr19:40878916 | C | T | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.675G>A | p.Ser225Ser | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/9 | 696/1760 | 675/1485 | 225/494 | chr19 | 40878916 | |||
chr19:40880134 | G | A | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.604C>T | p.Leu202Leu | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/9 | 625/1760 | 604/1485 | 202/494 | chr19 | 40880134 | |||
chr19:40880174 | C | T | 1 | a0001c0030 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.564G>A | p.Gly188Gly | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/9 | 585/1760 | 564/1485 | 188/494 | chr19 | 40880174 | |||
chr19:40880483 | C | A | 1 | a0019c0025 | 2 | HG01243.hp2 HG01928.hp2 |
synonymous_variant | LOW | c.489G>T | p.Thr163Thr | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 510/1760 | 489/1485 | 163/494 | chr19 | 40880483 | |||
chr19:40880566 | T | G | 2 | a0002c0038 a0019c0025 |
3 | HG01243.hp2 HG01928.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.406A>C | p.Arg136Arg | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 427/1760 | 406/1485 | 136/494 | chr19 | 40880566 | |||
chr19:40880582 | A | G | 25 | a0001c0001 a0001c0026 a0001c0030 others(22): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
synonymous_variant | LOW | c.390T>C | p.Phe130Phe | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 411/1760 | 390/1485 | 130/494 | chr19 | 40880582 | |||
chr19:40880621 | C | T | 7 | a0001c0026 a0002c0027 a0006c0021 others(4): Show |
10 | HG01243.hp2 HG01891.hp1 HG01928.hp2 others(7): Show |
synonymous_variant | LOW | c.351G>A | p.Ala117Ala | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/9 | 372/1760 | 351/1485 | 117/494 | chr19 | 40880621 | |||
chr19:40881715 | A | G | 24 | a0001c0001 a0001c0026 a0001c0030 others(21): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
synonymous_variant | LOW | c.217T>C | p.Leu73Leu | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/9 | 238/1760 | 217/1485 | 73/494 | chr19 | 40881715 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40875450 | G | A | 1 | a0009c0009t0013 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*243C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 243 | chr19 | 40875450 | ||||||
chr19:40875490 | T | G | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(18): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*203A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 203 | chr19 | 40875490 | ||||||
chr19:40875493 | C | T | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(18): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*200G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 200 | chr19 | 40875493 | ||||||
chr19:40875510 | G | C | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0026t0002 others(43): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*183C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 183 | chr19 | 40875510 | ||||||
chr19:40875512 | T | A | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0026t0002 others(43): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 181 | chr19 | 40875512 | ||||||
chr19:40875543 | G | C | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(52): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 150 | chr19 | 40875543 | ||||||
chr19:40875590 | C | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*103G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 103 | chr19 | 40875590 | ||||||
chr19:40875591 | G | C | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*102C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 102 | chr19 | 40875591 | ||||||
chr19:40875596 | T | C | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*97A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 97 | chr19 | 40875596 | ||||||
chr19:40875598 | C | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*95G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 95 | chr19 | 40875598 | ||||||
chr19:40875605 | T | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*88A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 88 | chr19 | 40875605 | ||||||
chr19:40875611 | T | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 82 | chr19 | 40875611 | ||||||
chr19:40875612 | A | C | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*81T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 81 | chr19 | 40875612 | ||||||
chr19:40875613 | C | T | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*80G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 80 | chr19 | 40875613 | ||||||
chr19:40875614 | C | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*79G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 79 | chr19 | 40875614 | ||||||
chr19:40875619 | T | C | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*74A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 74 | chr19 | 40875619 | ||||||
chr19:40875622 | T | C | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*71A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 71 | chr19 | 40875622 | ||||||
chr19:40875623 | C | T | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*70G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 70 | chr19 | 40875623 | ||||||
chr19:40875625 | G | C | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 68 | chr19 | 40875625 | ||||||
chr19:40875627 | G | A | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*66C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 66 | chr19 | 40875627 | ||||||
chr19:40875629 | A | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 64 | chr19 | 40875629 | ||||||
chr19:40875635 | C | T | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*58G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 58 | chr19 | 40875635 | ||||||
chr19:40875637 | C | T | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*56G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 56 | chr19 | 40875637 | ||||||
chr19:40875640 | A | G | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*53T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 53 | chr19 | 40875640 | ||||||
chr19:40875644 | C | T | 1 | a0019c0025t0010 | 2 | HG01243.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 49 | chr19 | 40875644 | ||||||
chr19:40875670 | A | C | 4 | a0003c0002t0008 a0003c0002t0009 a0007c0006t0011 others(1): Show |
5 | HG02451.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*23T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 9/9 | 23 | chr19 | 40875670 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40875935 | G | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(68): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1304-61C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40875935 | |||||||
chr19:40875963 | G | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(49): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1304-89C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40875963 | |||||||
chr19:40875970 | G | A | 13 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(10): Show |
15 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1304-96C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40875970 | |||||||
chr19:40875971 | G | A | 1 | a0019c0025t0010g0085 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1304-97C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40875971 | |||||||
chr19:40876031 | G | A | 4 | a0007c0006t0002g0024 a0007c0006t0002g0117 a0019c0025t0010g0085 others(1): Show |
6 | HG01243.hp2 HG01928.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1304-157C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876031 | |||||||
chr19:40876042 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1304-168G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876042 | |||||||
chr19:40876106 | C | T | 4 | a0002c0003t0001g0054 a0014c0015t0001g0123 a0019c0025t0010g0085 others(1): Show |
4 | HG01243.hp2 HG01928.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-232G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876106 | |||||||
chr19:40876225 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+302A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876225 | |||||||
chr19:40876232 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+295T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876232 | |||||||
chr19:40876275 | G | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(55): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1303+252C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876275 | |||||||
chr19:40876340 | C | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+187G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876340 | |||||||
chr19:40876352 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+175A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876352 | |||||||
chr19:40876407 | G | C | 1 | a0016c0020t0001g0025 | 3 | HG02109.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1303+120C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876407 | |||||||
chr19:40876466 | T | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+61A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876466 | |||||||
chr19:40876480 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+47C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876480 | |||||||
chr19:40876496 | A | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1303+31T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 8/8 | chr19 | 40876496 | |||||||
chr19:40876702 | A | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-34T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876702 | |||||||
chr19:40876703 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-35C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876703 | |||||||
chr19:40876707 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-39G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876707 | |||||||
chr19:40876708 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-40C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876708 | |||||||
chr19:40876740 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-72C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876740 | |||||||
chr19:40876748 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-80T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876748 | |||||||
chr19:40876750 | T | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-82A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876750 | |||||||
chr19:40876760 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(104): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1162-92C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876760 | |||||||
chr19:40876778 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-110G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876778 | |||||||
chr19:40876798 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-130C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876798 | |||||||
chr19:40876802 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-134T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876802 | |||||||
chr19:40876818 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-150T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876818 | |||||||
chr19:40876873 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-205A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876873 | |||||||
chr19:40876875 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-207C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876875 | |||||||
chr19:40876879 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-211G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876879 | |||||||
chr19:40876886 | T | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-218A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876886 | |||||||
chr19:40876902 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-234T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876902 | |||||||
chr19:40876907 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-239C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876907 | |||||||
chr19:40876907 | G | T | 1 | a0027c0040t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1162-239C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876907 | |||||||
chr19:40876916 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-248T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876916 | |||||||
chr19:40876928 | T | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1162-260A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876928 | |||||||
chr19:40876968 | T | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+222A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876968 | |||||||
chr19:40876974 | T | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+216A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876974 | |||||||
chr19:40876977 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+213T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876977 | |||||||
chr19:40876990 | C | T | 14 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(11): Show |
16 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1161+200G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40876990 | |||||||
chr19:40877007 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+183C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877007 | |||||||
chr19:40877048 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+142A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877048 | |||||||
chr19:40877071 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+119G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877071 | |||||||
chr19:40877100 | T | G | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+90A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877100 | |||||||
chr19:40877102 | A | T | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+88T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877102 | |||||||
chr19:40877103 | G | C | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+87C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877103 | |||||||
chr19:40877120 | G | T | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+70C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877120 | |||||||
chr19:40877124 | C | T | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+66G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877124 | |||||||
chr19:40877125 | A | G | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+65T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877125 | |||||||
chr19:40877130 | T | G | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+60A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877130 | |||||||
chr19:40877146 | A | G | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+44T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877146 | |||||||
chr19:40877149 | G | A | 13 | a0007c0006t0001g0110 a0007c0006t0002g0022 a0007c0006t0002g0023 others(10): Show |
19 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1161+41C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877149 | |||||||
chr19:40877161 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1161+29G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877161 | |||||||
chr19:40877169 | A | G | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+21T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877169 | |||||||
chr19:40877175 | T | TG | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+14dupC | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877175 | |||||||
chr19:40877180 | A | C | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+10T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 7/8 | chr19 | 40877180 | |||||||
chr19:40877380 | G | C | 2 | a0003c0002t0003g0140 a0003c0002t0003g0142 |
2 | NA18970.hp1 NA18983.hp2 |
splice_region_variant&intron_variant | LOW | c.974-3C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877380 | |||||||
chr19:40877411 | G | A | 6 | a0001c0001t0005g0066 a0001c0001t0006g0019 a0001c0001t0006g0072 others(3): Show |
10 | HG01109.hp1 HG01168.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.974-34C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877411 | |||||||
chr19:40877414 | A | G | 6 | a0001c0001t0005g0066 a0001c0001t0006g0019 a0001c0001t0006g0072 others(3): Show |
10 | HG01109.hp1 HG01168.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.974-37T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877414 | |||||||
chr19:40877439 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(109): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.974-62A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877439 | |||||||
chr19:40877447 | T | C | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-70A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877447 | |||||||
chr19:40877452 | C | T | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-75G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877452 | |||||||
chr19:40877466 | C | T | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-89G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877466 | |||||||
chr19:40877473 | C | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(113): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.974-96G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877473 | |||||||
chr19:40877473 | C | G | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-96G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877473 | |||||||
chr19:40877484 | G | A | 1 | a0027c0040t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.974-107C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877484 | |||||||
chr19:40877486 | A | G | 1 | a0007c0006t0002g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974-109T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877486 | |||||||
chr19:40877487 | G | A | 3 | a0018c0017t0001g0017 a0019c0025t0010g0085 a0019c0025t0010g0086 |
5 | HG01243.hp2 HG01928.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-110C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877487 | |||||||
chr19:40877516 | G | A | 15 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(12): Show |
19 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.974-139C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877516 | |||||||
chr19:40877523 | C | G | 1 | a0005c0005t0001g0033 | 2 | HG00741.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.974-146G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877523 | |||||||
chr19:40877596 | A | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.974-219T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877596 | |||||||
chr19:40877607 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.974-230C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877607 | |||||||
chr19:40877612 | G | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(109): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.974-235C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877612 | |||||||
chr19:40877619 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.973+233G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877619 | |||||||
chr19:40877687 | G | T | 14 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(11): Show |
16 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.973+165C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877687 | |||||||
chr19:40877746 | G | A | 1 | a0003c0002t0008g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.973+106C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877746 | |||||||
chr19:40877746 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.973+106C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877746 | |||||||
chr19:40877762 | T | C | 1 | a0019c0025t0010g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.973+90A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877762 | |||||||
chr19:40877779 | A | G | 3 | a0002c0038t0007g0048 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01928.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.973+73T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877779 | |||||||
chr19:40877784 | C | T | 2 | a0021c0023t0001g0090 a0021c0023t0001g0091 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.973+68G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877784 | |||||||
chr19:40877820 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG00733.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.973+32C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877820 | |||||||
chr19:40877834 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.973+18C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 6/8 | chr19 | 40877834 | |||||||
chr19:40878039 | C | T | 1 | a0003c0002t0003g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.832-46G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878039 | |||||||
chr19:40878084 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(34): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.832-91G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878084 | |||||||
chr19:40878162 | T | C | 20 | a0004c0004t0003g0098 a0004c0004t0004g0005 a0004c0004t0004g0099 others(17): Show |
60 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.832-169A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878162 | |||||||
chr19:40878179 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(109): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.832-186A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878179 | |||||||
chr19:40878197 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-204C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878197 | |||||||
chr19:40878197 | G | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.832-204C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878197 | |||||||
chr19:40878217 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-224A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878217 | |||||||
chr19:40878237 | A | AGTTTTTT others(3): Show |
2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-254_832-245dup others(10): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878237 | |||||||
chr19:40878248 | T | C | 1 | a0027c0040t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.832-255A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878248 | |||||||
chr19:40878253 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-260G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878253 | |||||||
chr19:40878284 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-291A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878284 | |||||||
chr19:40878291 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-298C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878291 | |||||||
chr19:40878300 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-307C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878300 | |||||||
chr19:40878318 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-325G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878318 | |||||||
chr19:40878322 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-329A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878322 | |||||||
chr19:40878350 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.832-357G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878350 | |||||||
chr19:40878406 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+354C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878406 | |||||||
chr19:40878413 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+347A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878413 | |||||||
chr19:40878429 | A | G | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+331T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878429 | |||||||
chr19:40878431 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+329C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878431 | |||||||
chr19:40878441 | A | G | 3 | a0002c0008t0001g0008 a0002c0008t0001g0045 a0002c0027t0001g0046 |
12 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.831+319T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878441 | |||||||
chr19:40878442 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+318C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878442 | |||||||
chr19:40878480 | T | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(107): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.831+280A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878480 | |||||||
chr19:40878481 | C | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(107): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.831+279G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878481 | |||||||
chr19:40878491 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+269G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878491 | |||||||
chr19:40878493 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+267A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878493 | |||||||
chr19:40878494 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+266C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878494 | |||||||
chr19:40878497 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+263C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878497 | |||||||
chr19:40878524 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+236T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878524 | |||||||
chr19:40878554 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+206A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878554 | |||||||
chr19:40878573 | G | T | 1 | a0002c0035t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.831+187C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878573 | |||||||
chr19:40878586 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.831+174G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878586 | |||||||
chr19:40878628 | G | A | 18 | a0003c0002t0003g0037 a0003c0002t0003g0038 a0003c0002t0003g0137 others(15): Show |
22 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.831+132C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878628 | |||||||
chr19:40878662 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+98G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878662 | |||||||
chr19:40878664 | A | G | 1 | a0001c0001t0002g0029 | 2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.831+96T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878664 | |||||||
chr19:40878672 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+88G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878672 | |||||||
chr19:40878673 | G | C | 27 | a0007c0006t0001g0110 a0007c0006t0002g0022 a0007c0006t0002g0023 others(24): Show |
37 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.831+87C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878673 | |||||||
chr19:40878676 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+84A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878676 | |||||||
chr19:40878684 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+76C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878684 | |||||||
chr19:40878691 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+69G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878691 | |||||||
chr19:40878705 | T | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+55A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878705 | |||||||
chr19:40878732 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.831+28G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878732 | |||||||
chr19:40878739 | G | A | 1 | a0001c0001t0006g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.831+21C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878739 | |||||||
chr19:40878742 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.831+18G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 5/8 | chr19 | 40878742 | |||||||
chr19:40879051 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-115T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879051 | |||||||
chr19:40879074 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-138A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879074 | |||||||
chr19:40879125 | C | T | 1 | a0010c0041t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655-189G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879125 | |||||||
chr19:40879156 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-220C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879156 | |||||||
chr19:40879179 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-243C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879179 | |||||||
chr19:40879180 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-244G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879180 | |||||||
chr19:40879184 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-248A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879184 | |||||||
chr19:40879210 | G | A | 13 | a0002c0008t0001g0008 a0002c0008t0001g0045 a0002c0008t0001g0047 others(10): Show |
36 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.655-274C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879210 | |||||||
chr19:40879227 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.655-291C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879227 | |||||||
chr19:40879296 | T | G | 1 | a0021c0023t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655-360A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879296 | |||||||
chr19:40879318 | A | G | 3 | a0010c0041t0001g0120 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01928.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.655-382T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879318 | |||||||
chr19:40879391 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-455A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879391 | |||||||
chr19:40879430 | C | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.655-494G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879430 | |||||||
chr19:40879455 | C | G | 12 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(9): Show |
14 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.655-519G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879455 | |||||||
chr19:40879467 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-531G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879467 | |||||||
chr19:40879475 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.655-539T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879475 | |||||||
chr19:40879529 | T | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(57): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.654+555A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879529 | |||||||
chr19:40879559 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.654+525C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879559 | |||||||
chr19:40879603 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.654+481G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879603 | |||||||
chr19:40879625 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.654+459C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879625 | |||||||
chr19:40879628 | G | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.654+456C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879628 | |||||||
chr19:40879722 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.654+362G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879722 | |||||||
chr19:40879729 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654+355C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879729 | |||||||
chr19:40879733 | C | G | 1 | a0001c0001t0002g0064 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.654+351G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879733 | |||||||
chr19:40879734 | G | C | 1 | a0019c0025t0010g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.654+350C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879734 | |||||||
chr19:40879749 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.654+335A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879749 | |||||||
chr19:40879829 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.654+255G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879829 | |||||||
chr19:40879863 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(109): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.654+221A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879863 | |||||||
chr19:40879869 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(109): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.654+215T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879869 | |||||||
chr19:40879877 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.654+207C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879877 | |||||||
chr19:40879895 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(55): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.654+189A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879895 | |||||||
chr19:40879926 | A | AGGGTATT others(13): Show |
5 | a0002c0003t0001g0018 a0002c0003t0003g0061 a0019c0025t0010g0085 others(2): Show |
7 | HG00621.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+157_654+158ins others(20): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879926 | |||||||
chr19:40879929 | C | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.654+155G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879929 | |||||||
chr19:40879965 | G | A | 5 | a0002c0003t0001g0018 a0002c0003t0003g0061 a0019c0025t0010g0085 others(2): Show |
7 | HG00621.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+119C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879965 | |||||||
chr19:40879993 | C | G | 5 | a0002c0003t0001g0018 a0002c0003t0003g0061 a0019c0025t0010g0085 others(2): Show |
7 | HG00621.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+91G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879993 | |||||||
chr19:40879995 | G | C | 5 | a0002c0003t0001g0018 a0002c0003t0003g0061 a0019c0025t0010g0085 others(2): Show |
7 | HG00621.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+89C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 4/8 | chr19 | 40879995 | |||||||
chr19:40880253 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.494-9C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880253 | |||||||
chr19:40880257 | A | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.494-13T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880257 | |||||||
chr19:40880264 | A | T | 1 | a0015c0018t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.494-20T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880264 | |||||||
chr19:40880266 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.494-22C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880266 | |||||||
chr19:40880266 | G | C | 20 | a0004c0004t0003g0098 a0004c0004t0004g0005 a0004c0004t0004g0099 others(17): Show |
60 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.494-22C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880266 | |||||||
chr19:40880304 | A | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.494-60T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880304 | |||||||
chr19:40880328 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.494-84A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880328 | |||||||
chr19:40880367 | A | G | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+112T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880367 | |||||||
chr19:40880370 | T | C | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+109A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880370 | |||||||
chr19:40880377 | G | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(38): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.493+102C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880377 | |||||||
chr19:40880390 | T | G | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+89A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880390 | |||||||
chr19:40880393 | T | G | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+86A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880393 | |||||||
chr19:40880397 | C | G | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+82G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880397 | |||||||
chr19:40880398 | A | G | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+81T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880398 | |||||||
chr19:40880402 | G | C | 3 | a0006c0028t0007g0044 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01928.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.493+77C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880402 | |||||||
chr19:40880406 | G | A | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+73C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880406 | |||||||
chr19:40880418 | C | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.493+61G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880418 | |||||||
chr19:40880424 | C | G | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+55G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880424 | |||||||
chr19:40880429 | T | C | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+50A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880429 | |||||||
chr19:40880436 | T | C | 1 | a0006c0028t0007g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+43A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880436 | |||||||
chr19:40880461 | T | G | 20 | a0004c0004t0003g0098 a0004c0004t0004g0005 a0004c0004t0004g0099 others(17): Show |
60 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.493+18A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880461 | |||||||
chr19:40880467 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.493+12T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880467 | |||||||
chr19:40880468 | A | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.493+11T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880468 | |||||||
chr19:40880471 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
splice_region_variant&intron_variant | LOW | c.493+8A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880471 | |||||||
chr19:40880473 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
splice_region_variant&intron_variant | LOW | c.493+6T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 3/8 | chr19 | 40880473 | |||||||
chr19:40880639 | C | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(59): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.344-11G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880639 | |||||||
chr19:40880642 | G | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(59): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.344-14C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880642 | |||||||
chr19:40880648 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-20C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880648 | |||||||
chr19:40880649 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-21C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880649 | |||||||
chr19:40880656 | G | C | 4 | a0006c0010t0001g0007 a0006c0016t0001g0015 a0019c0025t0010g0085 others(1): Show |
17 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.344-28C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880656 | |||||||
chr19:40880660 | T | C | 4 | a0006c0010t0001g0007 a0006c0016t0001g0015 a0019c0025t0010g0085 others(1): Show |
17 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.344-32A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880660 | |||||||
chr19:40880674 | T | G | 3 | a0001c0001t0002g0076 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01928.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.344-46A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880674 | |||||||
chr19:40880675 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.344-47C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880675 | |||||||
chr19:40880679 | G | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(55): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.344-51C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880679 | |||||||
chr19:40880687 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-59G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880687 | |||||||
chr19:40880691 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-63A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880691 | |||||||
chr19:40880705 | C | G | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-77G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880705 | |||||||
chr19:40880706 | C | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-78G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880706 | |||||||
chr19:40880707 | A | G | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-79T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880707 | |||||||
chr19:40880710 | G | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-82C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880710 | |||||||
chr19:40880712 | T | A | 6 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(3): Show |
6 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-84A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880712 | |||||||
chr19:40880713 | G | A | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-85C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880713 | |||||||
chr19:40880713 | G | GA | 4 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(1): Show |
4 | HG01123.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-86_344-85insT | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880713 | |||||||
chr19:40880713 | G | GAGAGAGA others(22): Show |
1 | a0013c0013t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.344-86_344-85insTC others(27): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880713 | |||||||
chr19:40880716 | GC | G | 6 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(3): Show |
6 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-89delG | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880716 | |||||||
chr19:40880717 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-89G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880717 | |||||||
chr19:40880717 | C | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(70): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.344-89G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880717 | |||||||
chr19:40880722 | G | A | 9 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(6): Show |
9 | HG01123.hp2 HG01243.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-94C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880722 | |||||||
chr19:40880724 | G | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-96C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880724 | |||||||
chr19:40880725 | T | G | 9 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(6): Show |
9 | HG01123.hp2 HG01243.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-97A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880725 | |||||||
chr19:40880728 | T | A | 5 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0115 others(2): Show |
5 | HG01496.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-100A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880728 | |||||||
chr19:40880729 | G | A | 4 | a0013c0013t0001g0114 a0019c0025t0010g0085 a0019c0025t0010g0086 others(1): Show |
4 | HG01123.hp2 HG01243.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-101C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880729 | |||||||
chr19:40880729 | G | GA | 4 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0115 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-102_344-101ins others(1): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880729 | |||||||
chr19:40880731 | G | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-103C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880731 | |||||||
chr19:40880733 | T | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-105A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880733 | |||||||
chr19:40880735 | G | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-107C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880735 | |||||||
chr19:40880744 | T | G | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-116A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880744 | |||||||
chr19:40880745 | G | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-117C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880745 | |||||||
chr19:40880746 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.344-118C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880746 | |||||||
chr19:40880747 | ATTC | A | 4 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0013c0013t0001g0115 others(1): Show |
4 | HG01123.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-122_344-120del others(3): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880747 | |||||||
chr19:40880748 | T | G | 1 | a0013c0013t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.344-120A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880748 | |||||||
chr19:40880749 | T | A | 1 | a0013c0013t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.344-121A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880749 | |||||||
chr19:40880749 | T | G | 2 | a0013c0013t0001g0087 a0013c0013t0001g0118 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.344-121A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880749 | |||||||
chr19:40880750 | C | A | 2 | a0013c0013t0001g0087 a0013c0013t0001g0118 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.344-122G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880750 | |||||||
chr19:40880750 | C | G | 1 | a0013c0013t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.344-122G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880750 | |||||||
chr19:40880753 | T | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-125A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880753 | |||||||
chr19:40880753 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-125A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880753 | |||||||
chr19:40880755 | C | A | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-127G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880755 | |||||||
chr19:40880756 | C | G | 7 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-128G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880756 | |||||||
chr19:40880758 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-130C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880758 | |||||||
chr19:40880758 | GTGCCC | G | 3 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0025c0039t0001g0084 |
3 | HG01884.hp1 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-135_344-131del others(5): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880758 | |||||||
chr19:40880759 | T | A | 4 | a0013c0013t0001g0114 a0013c0013t0001g0115 a0013c0013t0001g0116 others(1): Show |
4 | HG01123.hp2 HG01496.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-131A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880759 | |||||||
chr19:40880761 | C | A | 1 | a0013c0013t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.344-133G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880761 | |||||||
chr19:40880761 | C | G | 3 | a0013c0013t0001g0114 a0013c0013t0001g0115 a0013c0013t0001g0118 |
3 | HG01123.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344-133G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880761 | |||||||
chr19:40880762 | C | A | 4 | a0013c0013t0001g0114 a0013c0013t0001g0115 a0013c0013t0001g0116 others(1): Show |
4 | HG01123.hp2 HG01496.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-134G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880762 | |||||||
chr19:40880763 | C | G | 4 | a0013c0013t0001g0114 a0013c0013t0001g0115 a0013c0013t0001g0116 others(1): Show |
4 | HG01123.hp2 HG01496.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-135G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(29): Show |
C | 1 | a0001c0001t0002g0001 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.344-171_344-136del others(36): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(31): Show |
C | 2 | a0001c0001t0001g0003 a0001c0001t0002g0001 |
2 | HG03579.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.344-173_344-136del others(38): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(33): Show |
C | 2 | a0001c0001t0001g0003 a0001c0001t0002g0001 |
2 | HG02280.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.344-175_344-136del others(40): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(35): Show |
C | 1 | a0006c0021t0007g0164 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.344-177_344-136del others(42): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(37): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0008c0007t0009g0070 |
9 | HG01109.hp2 HG02970.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.344-179_344-136del others(44): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(39): Show |
C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0002g0001 others(10): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.344-181_344-136del others(46): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(41): Show |
C | 17 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0001c0001t0002g0029 others(14): Show |
38 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.344-183_344-136del others(48): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(43): Show |
C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0078 others(11): Show |
37 | HG00323.hp1 HG00733.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.344-185_344-136del others(50): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(45): Show |
C | 10 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0001c0001t0002g0080 others(7): Show |
18 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.344-187_344-136del others(52): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(47): Show |
C | 11 | a0001c0001t0001g0003 a0002c0003t0001g0002 a0002c0003t0001g0018 others(8): Show |
18 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-189_344-136del others(54): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(49): Show |
C | 9 | a0001c0001t0002g0001 a0002c0003t0001g0002 a0002c0003t0001g0049 others(6): Show |
23 | HG00099.hp2 HG00639.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.344-191_344-136del others(56): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(51): Show |
C | 13 | a0002c0003t0001g0002 a0002c0003t0001g0016 a0002c0003t0001g0054 others(10): Show |
42 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.344-193_344-136del others(58): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880763 | CAGGACAG others(55): Show |
C | 1 | a0006c0010t0001g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.344-197_344-136del others(62): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880763 | |||||||
chr19:40880766 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-138C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880766 | |||||||
chr19:40880768 | C | G | 9 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(6): Show |
9 | HG01123.hp2 HG01243.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-140G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880768 | |||||||
chr19:40880770 | GGTGCAAA others(3): Show |
G | 1 | a0013c0013t0001g0087 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.344-152_344-143del others(10): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880770 | |||||||
chr19:40880771 | G | A | 3 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0025c0039t0001g0084 |
3 | HG01123.hp2 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-143C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880771 | |||||||
chr19:40880771 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-143C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880771 | |||||||
chr19:40880772 | T | A | 2 | a0013c0013t0001g0115 a0013c0013t0001g0118 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344-144A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880772 | |||||||
chr19:40880772 | T | G | 3 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0025c0039t0001g0084 |
3 | HG01123.hp2 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-144A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880772 | |||||||
chr19:40880773 | G | A | 3 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0025c0039t0001g0084 |
3 | HG01123.hp2 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-145C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880773 | |||||||
chr19:40880774 | C | A | 2 | a0013c0013t0001g0115 a0013c0013t0001g0118 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344-146G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880774 | |||||||
chr19:40880774 | C | G | 3 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0025c0039t0001g0084 |
3 | HG01123.hp2 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-146G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880774 | |||||||
chr19:40880775 | A | G | 2 | a0013c0013t0001g0115 a0013c0013t0001g0118 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344-147T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880775 | |||||||
chr19:40880776 | A | G | 3 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0025c0039t0001g0084 |
3 | HG01123.hp2 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-148T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880776 | |||||||
chr19:40880777 | A | G | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-149T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880777 | |||||||
chr19:40880778 | C | A | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-150G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880778 | |||||||
chr19:40880778 | C | G | 4 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0013c0013t0001g0115 others(1): Show |
4 | HG01123.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-150G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880778 | |||||||
chr19:40880779 | T | A | 5 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0013c0013t0001g0115 others(2): Show |
5 | HG01123.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-151A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880779 | |||||||
chr19:40880780 | C | G | 5 | a0013c0013t0001g0113 a0013c0013t0001g0114 a0013c0013t0001g0115 others(2): Show |
5 | HG01123.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-152G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880780 | |||||||
chr19:40880783 | T | A | 6 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(3): Show |
6 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-155A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880783 | |||||||
chr19:40880783 | T | G | 1 | a0025c0039t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.344-155A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880783 | |||||||
chr19:40880784 | C | A | 1 | a0025c0039t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.344-156G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880784 | |||||||
chr19:40880784 | C | G | 6 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(3): Show |
6 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-156G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880784 | |||||||
chr19:40880789 | A | G | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-161T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880789 | |||||||
chr19:40880790 | A | G | 6 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(3): Show |
6 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-162T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880790 | |||||||
chr19:40880791 | A | G | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-163T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880791 | |||||||
chr19:40880792 | C | A | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-164G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880792 | |||||||
chr19:40880792 | C | G | 6 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(3): Show |
6 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-164G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880792 | |||||||
chr19:40880793 | A | G | 1 | a0013c0013t0001g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344-165T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880793 | |||||||
chr19:40880794 | C | A | 3 | a0013c0013t0001g0113 a0013c0013t0001g0115 a0013c0013t0001g0118 |
3 | HG02257.hp2 HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344-166G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880794 | |||||||
chr19:40880794 | C | G | 2 | a0013c0013t0001g0114 a0025c0039t0001g0084 |
2 | HG01123.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.344-166G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880794 | |||||||
chr19:40880796 | A | AGGGGGGG others(3): Show |
1 | a0010c0011t0001g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.344-169_344-168ins others(10): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880796 | |||||||
chr19:40880796 | A | AGGGGGGG others(4): Show |
1 | a0010c0011t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.344-169_344-168ins others(11): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880796 | |||||||
chr19:40880796 | A | AGGGGGGG others(6): Show |
1 | a0010c0011t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344-169_344-168ins others(13): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880796 | |||||||
chr19:40880797 | G | T | 1 | a0019c0025t0010g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.344-169C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880797 | |||||||
chr19:40880797 | GGGAGAGA others(24): Show |
G | 1 | a0004c0004t0005g0100 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.344-200_344-170del others(31): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880797 | |||||||
chr19:40880798 | G | A | 8 | a0013c0013t0001g0087 a0013c0013t0001g0113 a0013c0013t0001g0114 others(5): Show |
8 | HG01123.hp2 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.344-170C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GAGAGAGA others(20): Show |
1 | a0003c0002t0003g0158 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.344-171_344-170ins others(27): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGA | 4 | a0003c0002t0003g0112 a0003c0002t0003g0141 a0003c0002t0003g0142 others(1): Show |
4 | HG02155.hp2 HG03704.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-172_344-171dup others(2): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGA | 4 | a0003c0002t0003g0027 a0003c0002t0003g0145 a0003c0002t0009g0144 others(1): Show |
6 | HG02735.hp2 HG03098.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-174_344-171dup others(4): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGA | 2 | a0003c0002t0003g0014 a0003c0002t0003g0147 |
5 | HG00735.hp2 HG01978.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-176_344-171dup others(6): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(1): Show |
6 | a0003c0002t0002g0150 a0003c0002t0003g0039 a0003c0002t0003g0151 others(3): Show |
7 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-178_344-171dup others(8): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(3): Show |
2 | a0003c0002t0002g0152 a0007c0006t0002g0024 |
4 | HG02280.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-180_344-171dup others(10): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(5): Show |
2 | a0003c0002t0005g0153 a0003c0002t0008g0154 |
2 | NA18970.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.344-182_344-171dup others(12): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(7): Show |
1 | a0003c0002t0003g0040 | 2 | HG01346.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.344-184_344-171dup others(14): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(11): Show |
2 | a0003c0002t0004g0156 a0020c0024t0005g0155 |
2 | HG00609.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.344-188_344-171dup others(18): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(15): Show |
1 | a0003c0002t0004g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.344-192_344-171dup others(22): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(23): Show |
1 | a0003c0002t0004g0159 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.344-200_344-171dup others(30): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(27): Show |
1 | a0003c0002t0004g0160 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.344-204_344-171dup others(34): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(31): Show |
1 | a0003c0002t0004g0161 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.344-208_344-171dup others(38): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGAGAGAG others(47): Show |
1 | a0003c0002t0004g0162 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.344-224_344-171dup others(54): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGGGGGGG others(5): Show |
1 | a0010c0011t0001g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.344-171_344-170ins others(12): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GGGGGGGG others(18): Show |
1 | a0010c0011t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344-171_344-170ins others(25): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | G | GTCGAGGT others(102): Show |
1 | a0019c0025t0010g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.344-171_344-170ins others(109): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGA | G | 9 | a0003c0002t0003g0137 a0007c0006t0002g0107 a0007c0006t0002g0109 others(6): Show |
9 | HG00609.hp2 HG00639.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-172_344-171del others(2): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGA | G | 5 | a0003c0002t0003g0037 a0003c0002t0003g0135 a0003c0002t0006g0134 others(2): Show |
8 | HG01978.hp2 HG02027.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.344-174_344-171del others(4): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGA | G | 3 | a0003c0002t0004g0036 a0007c0006t0002g0106 a0007c0006t0011g0105 |
4 | HG02451.hp1 HG02717.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-176_344-171del others(6): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(1): Show |
G | 1 | a0007c0006t0002g0022 | 3 | HG02109.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.344-178_344-171del others(8): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(3): Show |
G | 2 | a0003c0002t0003g0132 a0007c0006t0002g0104 |
2 | HG02015.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.344-180_344-171del others(10): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(9): Show |
G | 1 | a0003c0002t0004g0131 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.344-186_344-171del others(16): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(15): Show |
G | 1 | a0003c0002t0005g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-192_344-171del others(22): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(21): Show |
G | 1 | a0004c0004t0004g0099 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.344-198_344-171del others(28): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(23): Show |
G | 2 | a0004c0004t0003g0098 a0005c0005t0001g0021 |
4 | HG02559.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-200_344-171del others(30): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(25): Show |
G | 16 | a0004c0004t0004g0005 a0004c0004t0005g0012 a0004c0004t0005g0089 others(13): Show |
54 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.344-202_344-171del others(32): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880798 | GGAGAGAG others(29): Show |
G | 2 | a0021c0023t0001g0090 a0021c0023t0001g0091 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.344-206_344-171del others(36): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880798 | |||||||
chr19:40880799 | G | T | 1 | a0019c0025t0010g0085 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.344-171C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880799 | |||||||
chr19:40880800 | A | G | 4 | a0010c0011t0001g0035 a0010c0011t0001g0103 a0014c0015t0001g0123 others(1): Show |
5 | HG00733.hp2 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-172T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880800 | |||||||
chr19:40880800 | A | T | 1 | a0001c0001t0002g0001 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.344-172T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880800 | |||||||
chr19:40880801 | G | GAGAGAGA others(13): Show |
1 | a0016c0020t0001g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.344-174_344-173ins others(20): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880801 | |||||||
chr19:40880802 | A | G | 5 | a0010c0011t0001g0119 a0010c0041t0001g0120 a0014c0015t0001g0121 others(2): Show |
6 | HG00609.hp2 HG00733.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-174T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880802 | |||||||
chr19:40880802 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0002g0001 |
2 | HG03579.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.344-174T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880802 | |||||||
chr19:40880804 | A | G | 6 | a0010c0011t0001g0119 a0010c0041t0001g0120 a0014c0015t0001g0121 others(3): Show |
7 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.344-176T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880804 | |||||||
chr19:40880804 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0002g0001 |
2 | HG02280.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.344-176T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880804 | |||||||
chr19:40880806 | A | G | 6 | a0010c0011t0001g0119 a0010c0041t0001g0120 a0014c0015t0001g0121 others(3): Show |
7 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.344-178T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880806 | |||||||
chr19:40880806 | A | T | 1 | a0006c0021t0007g0164 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.344-178T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880806 | |||||||
chr19:40880808 | A | G | 5 | a0010c0011t0001g0119 a0010c0041t0001g0120 a0014c0015t0001g0121 others(2): Show |
6 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-180T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880808 | |||||||
chr19:40880808 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0008c0007t0009g0070 |
9 | HG01109.hp2 HG02970.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.344-180T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880808 | |||||||
chr19:40880810 | A | AGAGAGAG others(96): Show |
1 | a0019c0025t0010g0085 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.344-183_344-182ins others(103): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880810 | |||||||
chr19:40880810 | A | G | 5 | a0010c0011t0001g0119 a0010c0041t0001g0120 a0014c0015t0001g0121 others(2): Show |
5 | HG00323.hp2 HG00609.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-182T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880810 | |||||||
chr19:40880810 | A | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0002g0001 others(10): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.344-182T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880810 | |||||||
chr19:40880812 | A | G | 1 | a0010c0011t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.344-184T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880812 | |||||||
chr19:40880812 | A | T | 17 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0001c0001t0002g0029 others(14): Show |
38 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.344-184T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880812 | |||||||
chr19:40880813 | G | GAGAGAGA others(3): Show |
1 | a0027c0040t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.344-186_344-185ins others(10): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880813 | |||||||
chr19:40880814 | A | G | 1 | a0010c0011t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.344-186T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880814 | |||||||
chr19:40880814 | A | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0078 others(11): Show |
37 | HG00323.hp1 HG00733.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.344-186T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880814 | |||||||
chr19:40880816 | A | G | 1 | a0010c0011t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.344-188T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880816 | |||||||
chr19:40880816 | A | T | 10 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0001c0001t0002g0080 others(7): Show |
18 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.344-188T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880816 | |||||||
chr19:40880818 | A | T | 11 | a0001c0001t0001g0003 a0002c0003t0001g0002 a0002c0003t0001g0018 others(8): Show |
18 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-190T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880818 | |||||||
chr19:40880820 | A | T | 9 | a0001c0001t0002g0001 a0002c0003t0001g0002 a0002c0003t0001g0049 others(6): Show |
23 | HG00099.hp2 HG00639.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.344-192T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880820 | |||||||
chr19:40880822 | A | T | 13 | a0002c0003t0001g0002 a0002c0003t0001g0016 a0002c0003t0001g0054 others(10): Show |
42 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.344-194T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880822 | |||||||
chr19:40880826 | A | T | 1 | a0006c0010t0001g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.344-198T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880826 | |||||||
chr19:40880840 | A | AGAGAGAG others(10): Show |
1 | a0003c0002t0005g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.344-229_344-213dup others(17): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880840 | |||||||
chr19:40880852 | A | AGAGAGAG others(16): Show |
1 | a0003c0002t0005g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.344-225_344-224ins others(23): Show |
CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880852 | |||||||
chr19:40880864 | C | A | 1 | a0002c0008t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.344-236G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880864 | |||||||
chr19:40880865 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-237C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880865 | |||||||
chr19:40880869 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-241T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880869 | |||||||
chr19:40880870 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-242C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880870 | |||||||
chr19:40880882 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-254C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880882 | |||||||
chr19:40880891 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-263C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880891 | |||||||
chr19:40880909 | A | G | 12 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(9): Show |
14 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.344-281T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880909 | |||||||
chr19:40880910 | T | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-282A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880910 | |||||||
chr19:40880918 | C | T | 1 | a0002c0003t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.344-290G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880918 | |||||||
chr19:40880919 | G | A | 4 | a0006c0022t0002g0028 a0006c0028t0007g0044 a0019c0025t0010g0085 others(1): Show |
5 | HG01243.hp2 HG01891.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-291C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880919 | |||||||
chr19:40880922 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-294C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880922 | |||||||
chr19:40880944 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-316A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880944 | |||||||
chr19:40880952 | G | A | 14 | a0010c0011t0001g0035 a0010c0011t0001g0102 a0010c0011t0001g0103 others(11): Show |
18 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-324C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880952 | |||||||
chr19:40880962 | T | A | 3 | a0001c0001t0001g0078 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01928.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.344-334A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880962 | |||||||
chr19:40880968 | G | A | 1 | a0009c0009t0001g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.344-340C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880968 | |||||||
chr19:40880969 | T | G | 1 | a0009c0009t0001g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.344-341A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880969 | |||||||
chr19:40880970 | G | T | 1 | a0009c0009t0001g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.344-342C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880970 | |||||||
chr19:40880986 | A | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(60): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.344-358T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40880986 | |||||||
chr19:40881061 | C | G | 10 | a0002c0008t0001g0008 a0002c0008t0001g0045 a0002c0008t0001g0047 others(7): Show |
32 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.344-433G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881061 | |||||||
chr19:40881077 | T | A | 1 | a0002c0003t0001g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.344-449A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881077 | |||||||
chr19:40881096 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-468G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881096 | |||||||
chr19:40881102 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.344-474G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881102 | |||||||
chr19:40881157 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+432C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881157 | |||||||
chr19:40881171 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+418T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881171 | |||||||
chr19:40881177 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+412C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881177 | |||||||
chr19:40881179 | A | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+410T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881179 | |||||||
chr19:40881192 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+397C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881192 | |||||||
chr19:40881193 | G | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+396C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881193 | |||||||
chr19:40881201 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+388T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881201 | |||||||
chr19:40881210 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+379C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881210 | |||||||
chr19:40881216 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+373T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881216 | |||||||
chr19:40881218 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+371A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881218 | |||||||
chr19:40881226 | G | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+363C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881226 | |||||||
chr19:40881235 | T | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+354A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881235 | |||||||
chr19:40881236 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+353C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881236 | |||||||
chr19:40881240 | A | C | 1 | a0002c0008t0001g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343+349T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881240 | |||||||
chr19:40881244 | A | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+345T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881244 | |||||||
chr19:40881249 | A | G | 22 | a0004c0004t0003g0098 a0004c0004t0004g0005 a0004c0004t0004g0099 others(19): Show |
62 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.343+340T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881249 | |||||||
chr19:40881253 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+336C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881253 | |||||||
chr19:40881258 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+331G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881258 | |||||||
chr19:40881259 | A | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+330T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881259 | |||||||
chr19:40881284 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+305C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881284 | |||||||
chr19:40881319 | C | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+270G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881319 | |||||||
chr19:40881336 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(56): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.343+253C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881336 | |||||||
chr19:40881395 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.343+194C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881395 | |||||||
chr19:40881401 | C | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(61): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.343+188G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881401 | |||||||
chr19:40881410 | C | T | 1 | a0027c0040t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.343+179G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881410 | |||||||
chr19:40881411 | G | A | 1 | a0031c0032t0001g0082 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.343+178C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881411 | |||||||
chr19:40881421 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.343+168C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881421 | |||||||
chr19:40881449 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+140C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881449 | |||||||
chr19:40881467 | A | G | 3 | a0013c0013t0001g0087 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01884.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.343+122T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881467 | |||||||
chr19:40881468 | T | G | 3 | a0013c0013t0001g0087 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01884.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.343+121A>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881468 | |||||||
chr19:40881479 | C | T | 3 | a0013c0013t0001g0087 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01884.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.343+110G>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881479 | |||||||
chr19:40881484 | G | A | 3 | a0013c0013t0001g0087 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01884.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.343+105C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881484 | |||||||
chr19:40881485 | T | C | 3 | a0013c0013t0001g0087 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01884.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.343+104A>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881485 | |||||||
chr19:40881492 | A | G | 22 | a0004c0004t0003g0098 a0004c0004t0004g0005 a0004c0004t0004g0099 others(19): Show |
62 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.343+97T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881492 | |||||||
chr19:40881492 | A | T | 3 | a0007c0006t0004g0088 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG00639.hp2 HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+97T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881492 | |||||||
chr19:40881504 | G | T | 3 | a0013c0013t0001g0087 a0019c0025t0010g0085 a0019c0025t0010g0086 |
3 | HG01243.hp2 HG01884.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.343+85C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881504 | |||||||
chr19:40881531 | C | G | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+58G>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881531 | |||||||
chr19:40881544 | A | G | 5 | a0006c0021t0007g0163 a0006c0021t0007g0164 a0006c0022t0002g0028 others(2): Show |
6 | HG01891.hp1 HG02486.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.343+45T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881544 | |||||||
chr19:40881544 | A | T | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+45T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881544 | |||||||
chr19:40881553 | G | A | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+36C>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881553 | |||||||
chr19:40881570 | A | C | 2 | a0019c0025t0010g0085 a0019c0025t0010g0086 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.343+19T>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 2/8 | chr19 | 40881570 | |||||||
chr19:40881764 | A | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0077 others(117): Show |
336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.181-13T>C | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 1/8 | chr19 | 40881764 | |||||||
chr19:40881797 | T | A | 2 | a0006c0021t0007g0163 a0006c0021t0007g0164 |
2 | HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.181-46A>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 1/8 | chr19 | 40881797 | |||||||
chr19:40881798 | G | T | 1 | a0002c0008t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181-47C>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 1/8 | chr19 | 40881798 | |||||||
chr19:40881818 | A | T | 1 | a0009c0009t0001g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.181-67T>A | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 1/8 | chr19 | 40881818 | |||||||
chr19:40881928 | C | A | 1 | a0002c0035t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.180+103G>T | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 1/8 | chr19 | 40881928 | |||||||
chr19:40882002 | G | C | 2 | a0006c0010t0001g0007 a0006c0016t0001g0015 |
15 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.180+29C>G | CYP2A7 | ENSG00000198077.11 | transcript | ENST00000301146.9 | protein_coding | 1/8 | chr19 | 40882002 |