Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8170 |
| ensemblid | ENSG00000132874.15 |
| hgncid | 10919 |
| symbol | SLC14A2 |
| name | solute carrier family 14 member 2 |
| refseq_nuc | NM_007163.4 |
| refseq_prot | NP_009094.3 |
| ensembl_nuc | ENST00000255226.11 |
| ensembl_prot | ENSP00000255226.5 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 45615476 |
| end | 45683688 |
| strand | + |
| ver | v1.2 |
| region | chr18:45615476-45683688 |
| region5000 | chr18:45610476-45688688 |
| regionname0 | SLC14A2_chr18_45615476_45683688 |
| regionname5000 | SLC14A2_chr18_45610476_45688688 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 920 | 94 | 25 | 13 | 44 | 3 | 9 | 36 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0002 | 0/1 | 920 | 82 | 18 | 16 | 39 | 2 | 6 | 33 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0003 | 0/0 | 920 | 58 | 18 | 15 | 17 | 5 | 3 | 12 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0004 | 0/0 | 920 | 55 | 1 | 9 | 36 | 1 | 8 | 19 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0005 | 0/0 | 920 | 27 | 6 | 4 | 14 | 0 | 3 | 12 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0006 | 0/0 | 920 | 20 | 3 | 8 | 2 | 3 | 4 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0007 | 0/0 | 920 | 13 | 0 | 2 | 10 | 0 | 1 | 10 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0008 | 1/0 | 920 | 9 | 5 | 0 | 3 | 0 | 0 | 3 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0009 | 0/0 | 920 | 7 | 0 | 3 | 4 | 0 | 0 | 4 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0010 | 0/0 | 920 | 6 | 1 | 0 | 5 | 0 | 0 | 4 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0011 | 0/0 | 920 | 5 | 2 | 0 | 2 | 1 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0012 | 0/0 | 920 | 5 | 4 | 0 | 1 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0013 | 0/0 | 920 | 4 | 0 | 0 | 3 | 0 | 1 | 3 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0014 | 0/0 | 920 | 3 | 1 | 1 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0015 | 0/0 | 920 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0016 | 0/0 | 920 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0017 | 0/0 | 920 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0018 | 0/0 | 920 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0019 | 0/0 | 920 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0020 | 0/0 | 920 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0021 | 0/0 | 920 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0022 | 0/0 | 920 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0023 | 0/0 | 920 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0024 | 0/0 | 920 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| a0025 | 0/0 | 920 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | MSDPH others(915): Show |
chr18 | 45610476 | 45688688 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2760 | 56 | 14 | 3 | 34 | 0 | 5 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0001c0004 | 0/0 | 2760 | 35 | 9 | 9 | 10 | 3 | 4 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0001c0022 | 0/0 | 2760 | 2 | 1 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0001c0023 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0002c0001 | 0/1 | 2760 | 82 | 18 | 16 | 39 | 2 | 6 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0003c0005 | 0/0 | 2760 | 31 | 10 | 5 | 14 | 1 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0003c0006 | 0/0 | 2760 | 23 | 7 | 8 | 3 | 3 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0003c0018 | 0/0 | 2760 | 3 | 0 | 2 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0003c0033 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0004c0003 | 0/0 | 2760 | 52 | 1 | 9 | 33 | 1 | 8 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0004c0019 | 0/0 | 2760 | 3 | 0 | 0 | 3 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0005c0008 | 0/0 | 2760 | 16 | 1 | 1 | 12 | 0 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0005c0010 | 0/0 | 2760 | 11 | 5 | 3 | 2 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0006c0007 | 0/0 | 2760 | 20 | 3 | 8 | 2 | 3 | 4 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0007c0009 | 0/0 | 2760 | 13 | 0 | 2 | 10 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0008c0011 | 1/0 | 2760 | 8 | 4 | 0 | 3 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0008c0025 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0009c0012 | 0/0 | 2760 | 6 | 0 | 2 | 4 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0009c0035 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0010c0014 | 0/0 | 2760 | 5 | 1 | 0 | 4 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0010c0024 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0011c0015 | 0/0 | 2760 | 5 | 2 | 0 | 2 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0012c0013 | 0/0 | 2760 | 5 | 4 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0013c0016 | 0/0 | 2760 | 4 | 0 | 0 | 3 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0014c0020 | 0/0 | 2760 | 3 | 1 | 1 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0015c0017 | 0/0 | 2760 | 3 | 3 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0016c0021 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 0 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0017c0036 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0018c0028 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0019c0031 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0020c0026 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0021c0029 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0022c0027 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0023c0032 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0024c0034 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 | ||
| a0025c0030 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ATGTC others(2755): Show |
chr18 | 45610476 | 45688688 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003 | 0/0 | 4073 | 43 | 6 | 2 | 32 | 0 | 3 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0002t0004 | 0/0 | 4073 | 7 | 3 | 0 | 2 | 0 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0002t0008 | 0/0 | 4073 | 6 | 5 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0004t0003 | 0/0 | 4073 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0004t0004 | 0/0 | 4073 | 31 | 8 | 8 | 10 | 3 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0004t0013 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0001c0004t0016 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0001c0004t0023 | 0/0 | 4073 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0022t0004 | 0/0 | 4073 | 2 | 1 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0001c0023t0003 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0001 | 0/0 | 4072 | 14 | 0 | 1 | 11 | 0 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0002 | 0/0 | 4073 | 45 | 14 | 8 | 17 | 2 | 4 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0005 | 0/0 | 4073 | 14 | 0 | 4 | 10 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0006 | 0/0 | 4074 | 5 | 4 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0011 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0015 | 0/0 | 4073 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0018 | 0/1 | 4073 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0002c0001t0019 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0003c0005t0001 | 0/0 | 4072 | 7 | 0 | 0 | 7 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0003c0005t0002 | 0/0 | 4073 | 14 | 2 | 5 | 5 | 1 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0003c0005t0005 | 0/0 | 4073 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0003c0005t0006 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0003c0005t0007 | 0/0 | 4073 | 6 | 6 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0003c0005t0017 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0003c0006t0001 | 0/0 | 4072 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0003c0006t0002 | 0/0 | 4073 | 18 | 6 | 7 | 1 | 3 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0003c0006t0006 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0003c0006t0011 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0003c0006t0012 | 0/0 | 4072 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0003c0018t0002 | 0/0 | 4073 | 3 | 0 | 2 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0003c0033t0002 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0004c0003t0001 | 0/0 | 4072 | 49 | 1 | 9 | 33 | 1 | 5 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0004c0003t0005 | 0/0 | 4073 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0004c0003t0020 | 0/0 | 4072 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0004c0003t0021 | 0/0 | 4072 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0004c0019t0001 | 0/0 | 4072 | 3 | 0 | 0 | 3 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0005c0008t0003 | 0/0 | 4073 | 15 | 0 | 1 | 12 | 0 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0005c0008t0004 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0005c0010t0003 | 0/0 | 4073 | 3 | 0 | 3 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0005c0010t0004 | 0/0 | 4073 | 5 | 3 | 0 | 1 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0005c0010t0013 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0005c0010t0014 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4069): Show |
chr18 | 45610476 | 45688688 |
| a0006c0007t0003 | 0/0 | 4073 | 14 | 2 | 4 | 2 | 3 | 3 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0006c0007t0004 | 0/0 | 4073 | 6 | 1 | 4 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0007c0009t0001 | 0/0 | 4072 | 13 | 0 | 2 | 10 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0008c0011t0001 | 0/0 | 4072 | 2 | 2 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0008c0011t0002 | 1/0 | 4073 | 3 | 2 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0008c0011t0005 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0008c0011t0010 | 0/0 | 4073 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0008c0025t0009 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0009c0012t0002 | 0/0 | 4073 | 3 | 0 | 1 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0009c0012t0005 | 0/0 | 4073 | 3 | 0 | 1 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0009c0035t0002 | 0/0 | 4073 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0010c0014t0001 | 0/0 | 4072 | 5 | 1 | 0 | 4 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0010c0024t0001 | 0/0 | 4072 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0011c0015t0003 | 0/0 | 4073 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0011c0015t0004 | 0/0 | 4073 | 3 | 2 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0012c0013t0003 | 0/0 | 4073 | 4 | 3 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0012c0013t0022 | 0/0 | 4072 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0013c0016t0001 | 0/0 | 4072 | 4 | 0 | 0 | 3 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4067): Show |
chr18 | 45610476 | 45688688 |
| a0014c0020t0004 | 0/0 | 4073 | 3 | 1 | 1 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0015c0017t0002 | 0/0 | 4073 | 3 | 3 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0016c0021t0005 | 0/0 | 4073 | 2 | 0 | 0 | 0 | 0 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0017c0036t0002 | 0/0 | 4073 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0018c0028t0002 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0019c0031t0003 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0020c0026t0004 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0021c0029t0004 | 0/0 | 4073 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0022c0027t0009 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0023c0032t0002 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0024c0034t0009 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| a0025c0030t0004 | 0/0 | 4073 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | ACACC others(4068): Show |
chr18 | 45610476 | 45688688 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0002t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0013g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0016g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0004t0023g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0022t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0022t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0001c0023t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0011g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0015g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0018g0381 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0002c0001t0019g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0005g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0005t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0011g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0012g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0006t0012g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0018t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0018t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0018t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0003c0033t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0020g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0003t0021g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0019t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0019t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0004c0019t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0008t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0005c0010t0014g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0002 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0006c0007t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0007c0009t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0002g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0011t0010g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0008c0025t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0012t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0012t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0012t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0012t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0012t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0012t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0009c0035t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0010c0014t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0010c0014t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0010c0014t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0010c0014t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0010c0014t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0010c0024t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0011c0015t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0011c0015t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0011c0015t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0011c0015t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0011c0015t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0012c0013t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0012c0013t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0012c0013t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0012c0013t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0012c0013t0022g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0013c0016t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0013c0016t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0013c0016t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0013c0016t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0014c0020t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0014c0020t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0014c0020t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0015c0017t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0015c0017t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0015c0017t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0016c0021t0005g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0016c0021t0005g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0017c0036t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0018c0028t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0019c0031t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0020c0026t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0021c0029t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0022c0027t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0023c0032t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0024c0034t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| a0025c0030t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0006 | c0007 | t0003 | g0058 | EUR | GBR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00099 | hp2 | a0001 | c0004 | t0004 | g0261 | EUR | GBR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0224 | EUR | GBR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00140 | hp2 | a0011 | c0015 | t0004 | g0021 | EUR | GBR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00280 | hp1 | a0003 | c0006 | t0002 | g0318 | EUR | FIN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00280 | hp2 | a0006 | c0007 | t0003 | g0002 | EUR | FIN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00323 | hp1 | a0003 | c0006 | t0002 | g0067 | EUR | FIN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00323 | hp2 | a0006 | c0007 | t0003 | g0343 | EUR | FIN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00423 | hp1 | a0004 | c0003 | t0001 | g0289 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00423 | hp2 | a0001 | c0004 | t0004 | g0313 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00438 | hp1 | a0003 | c0005 | t0005 | g0357 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00438 | hp2 | a0004 | c0003 | t0001 | g0317 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00544 | hp1 | a0004 | c0003 | t0001 | g0075 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00544 | hp2 | a0004 | c0003 | t0001 | g0011 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0332 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00609 | hp2 | a0003 | c0005 | t0002 | g0329 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0355 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00621 | hp2 | a0005 | c0008 | t0003 | g0231 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00642 | hp1 | a0006 | c0007 | t0004 | g0184 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00642 | hp2 | a0005 | c0010 | t0003 | g0196 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00673 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00673 | hp2 | a0004 | c0019 | t0001 | g0264 | EAS | CHS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00733 | hp1 | a0001 | c0004 | t0004 | g0020 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00733 | hp2 | a0009 | c0012 | t0005 | g0241 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00735 | hp1 | a0001 | c0004 | t0004 | g0098 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00735 | hp2 | a0003 | c0005 | t0002 | g0139 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00738 | hp1 | a0005 | c0008 | t0003 | g0202 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00738 | hp2 | a0003 | c0006 | t0002 | g0145 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00741 | hp1 | a0001 | c0004 | t0004 | g0260 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG00741 | hp2 | a0002 | c0001 | t0011 | g0024 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01070 | hp1 | a0002 | c0001 | t0015 | g0016 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01070 | hp2 | a0003 | c0018 | t0002 | g0135 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01071 | hp1 | a0001 | c0004 | t0004 | g0276 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01071 | hp2 | a0003 | c0018 | t0002 | g0136 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01074 | hp1 | a0004 | c0003 | t0001 | g0292 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01074 | hp2 | a0005 | c0010 | t0003 | g0197 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01081 | hp1 | a0003 | c0006 | t0002 | g0281 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01081 | hp2 | a0006 | c0007 | t0004 | g0279 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01099 | hp1 | a0004 | c0003 | t0001 | g0137 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01099 | hp2 | a0004 | c0003 | t0001 | g0029 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01106 | hp1 | a0001 | c0004 | t0004 | g0227 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01106 | hp2 | a0004 | c0003 | t0001 | g0336 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01109 | hp1 | a0002 | c0001 | t0002 | g0064 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01109 | hp2 | a0002 | c0001 | t0006 | g0080 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01167 | hp1 | a0002 | c0001 | t0002 | g0287 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01167 | hp2 | a0004 | c0003 | t0001 | g0138 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01168 | hp1 | a0007 | c0009 | t0001 | g0132 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01168 | hp2 | a0002 | c0001 | t0002 | g0019 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01169 | hp1 | a0002 | c0001 | t0002 | g0018 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01169 | hp2 | a0002 | c0001 | t0002 | g0286 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01192 | hp1 | a0001 | c0022 | t0004 | g0338 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01192 | hp2 | a0002 | c0001 | t0005 | g0337 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0017 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01243 | hp2 | a0014 | c0020 | t0004 | g0275 | AMR | PUR | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01255 | hp1 | a0006 | c0007 | t0004 | g0223 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01255 | hp2 | a0003 | c0006 | t0002 | g0233 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01256 | hp1 | a0002 | c0001 | t0002 | g0068 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01256 | hp2 | a0003 | c0006 | t0002 | g0013 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01257 | hp1 | a0007 | c0009 | t0001 | g0001 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01257 | hp2 | a0003 | c0005 | t0002 | g0158 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01258 | hp1 | a0003 | c0005 | t0002 | g0004 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01258 | hp2 | a0003 | c0006 | t0002 | g0013 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01261 | hp1 | a0001 | c0004 | t0003 | g0051 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01261 | hp2 | a0002 | c0001 | t0002 | g0225 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0071 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01346 | hp2 | a0003 | c0006 | t0002 | g0229 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01358 | hp1 | a0006 | c0007 | t0003 | g0028 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01358 | hp2 | a0002 | c0001 | t0005 | g0333 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01433 | hp1 | a0002 | c0001 | t0005 | g0153 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01433 | hp2 | a0017 | c0036 | t0002 | g0288 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01496 | hp1 | a0001 | c0004 | t0004 | g0282 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01496 | hp2 | a0001 | c0002 | t0008 | g0255 | AMR | CLM | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01516 | hp1 | a0003 | c0018 | t0002 | g0030 | EUR | IBS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01516 | hp2 | a0001 | c0004 | t0004 | g0277 | EUR | IBS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01517 | hp1 | a0001 | c0004 | t0004 | g0278 | EUR | IBS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01517 | hp2 | a0003 | c0005 | t0002 | g0297 | EUR | IBS | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01884 | hp1 | a0005 | c0010 | t0014 | g0012 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01884 | hp2 | a0001 | c0002 | t0008 | g0143 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01891 | hp1 | a0003 | c0006 | t0002 | g0147 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01928 | hp1 | a0006 | c0007 | t0003 | g0114 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01928 | hp2 | a0001 | c0004 | t0004 | g0368 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01934 | hp1 | a0009 | c0035 | t0002 | g0217 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0226 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01952 | hp1 | a0003 | c0005 | t0002 | g0161 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01952 | hp2 | a0004 | c0003 | t0001 | g0335 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01975 | hp1 | a0003 | c0006 | t0011 | g0169 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0027 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01978 | hp1 | a0006 | c0007 | t0003 | g0160 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01978 | hp2 | a0004 | c0003 | t0001 | g0273 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01981 | hp1 | a0006 | c0007 | t0004 | g0183 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01981 | hp2 | a0003 | c0006 | t0002 | g0263 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01993 | hp1 | a0002 | c0001 | t0005 | g0334 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG01993 | hp2 | a0001 | c0004 | t0004 | g0351 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02015 | hp1 | a0014 | c0020 | t0004 | g0274 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02015 | hp2 | a0002 | c0001 | t0002 | g0359 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02027 | hp1 | a0004 | c0003 | t0001 | g0353 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02027 | hp2 | a0004 | c0003 | t0001 | g0162 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02040 | hp1 | a0006 | c0007 | t0003 | g0243 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02040 | hp2 | a0004 | c0003 | t0001 | g0291 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02055 | hp1 | a0002 | c0001 | t0002 | g0129 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02055 | hp2 | a0012 | c0013 | t0003 | g0201 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02056 | hp1 | a0003 | c0005 | t0002 | g0344 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02074 | hp1 | a0010 | c0014 | t0001 | g0213 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0285 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02083 | hp1 | a0004 | c0003 | t0001 | g0354 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02083 | hp2 | a0004 | c0003 | t0001 | g0314 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02129 | hp1 | a0003 | c0006 | t0002 | g0375 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02129 | hp2 | a0004 | c0003 | t0001 | g0120 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02132 | hp1 | a0002 | c0001 | t0002 | g0358 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02132 | hp2 | a0004 | c0019 | t0001 | g0093 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02135 | hp1 | a0004 | c0003 | t0001 | g0094 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02135 | hp2 | a0004 | c0003 | t0001 | g0316 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02145 | hp1 | a0001 | c0022 | t0004 | g0339 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0250 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02148 | hp1 | a0003 | c0005 | t0002 | g0004 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02148 | hp2 | a0009 | c0012 | t0002 | g0239 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02155 | hp1 | a0003 | c0005 | t0001 | g0081 | EAS | CDX | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0101 | EAS | CDX | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02165 | hp1 | a0005 | c0008 | t0003 | g0210 | EAS | CDX | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02165 | hp2 | a0001 | c0004 | t0004 | g0340 | EAS | CDX | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02257 | hp1 | a0003 | c0006 | t0002 | g0305 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02257 | hp2 | a0001 | c0004 | t0004 | g0307 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02258 | hp1 | a0006 | c0007 | t0003 | g0149 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02258 | hp2 | a0001 | c0023 | t0003 | g0374 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02273 | hp1 | a0004 | c0003 | t0001 | g0341 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02273 | hp2 | a0004 | c0003 | t0001 | g0159 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0376 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02280 | hp2 | a0002 | c0001 | t0002 | g0015 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02293 | hp1 | a0006 | c0007 | t0003 | g0164 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02293 | hp2 | a0005 | c0010 | t0003 | g0234 | AMR | PEL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02523 | hp1 | a0004 | c0003 | t0001 | g0315 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02523 | hp2 | a0002 | c0001 | t0002 | g0290 | EAS | KHV | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02572 | hp1 | a0005 | c0010 | t0004 | g0176 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02602 | hp1 | a0002 | c0001 | t0002 | g0066 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02602 | hp2 | a0001 | c0004 | t0004 | g0065 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02615 | hp1 | a0002 | c0001 | t0002 | g0023 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02615 | hp2 | a0012 | c0013 | t0003 | g0235 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02622 | hp1 | a0001 | c0004 | t0004 | g0306 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02622 | hp2 | a0002 | c0001 | t0002 | g0193 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02630 | hp1 | a0002 | c0001 | t0002 | g0130 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02630 | hp2 | a0003 | c0005 | t0007 | g0049 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02647 | hp1 | a0003 | c0005 | t0007 | g0267 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02647 | hp2 | a0001 | c0002 | t0008 | g0249 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02683 | hp1 | a0004 | c0003 | t0001 | g0308 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02683 | hp2 | a0003 | c0006 | t0002 | g0052 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02698 | hp1 | a0004 | c0003 | t0001 | g0324 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0361 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02717 | hp1 | a0003 | c0005 | t0002 | g0140 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0309 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02723 | hp2 | a0003 | c0033 | t0002 | g0134 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02735 | hp1 | a0004 | c0003 | t0001 | g0323 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02735 | hp2 | a0006 | c0007 | t0003 | g0057 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02738 | hp1 | a0001 | c0004 | t0004 | g0186 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02738 | hp2 | a0003 | c0006 | t0006 | g0185 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02809 | hp1 | a0018 | c0028 | t0002 | g0045 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02809 | hp2 | a0008 | c0011 | t0001 | g0174 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02818 | hp1 | a0001 | c0002 | t0008 | g0350 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02818 | hp2 | a0001 | c0004 | t0004 | g0148 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02886 | hp1 | a0006 | c0007 | t0004 | g0170 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02886 | hp2 | a0010 | c0014 | t0001 | g0221 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02895 | hp1 | a0002 | c0001 | t0006 | g0166 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02895 | hp2 | a0003 | c0005 | t0007 | g0295 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02896 | hp1 | a0011 | c0015 | t0004 | g0300 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02896 | hp2 | a0002 | c0001 | t0006 | g0111 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02897 | hp1 | a0002 | c0001 | t0006 | g0125 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02897 | hp2 | a0011 | c0015 | t0004 | g0299 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02922 | hp1 | a0008 | c0025 | t0009 | g0203 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02922 | hp2 | a0003 | c0006 | t0002 | g0165 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02965 | hp1 | a0005 | c0010 | t0014 | g0012 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02965 | hp2 | a0015 | c0017 | t0002 | g0042 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02970 | hp1 | a0002 | c0001 | t0002 | g0378 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02970 | hp2 | a0003 | c0005 | t0007 | g0048 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0242 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02976 | hp2 | a0012 | c0013 | t0003 | g0200 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03041 | hp1 | a0014 | c0020 | t0004 | g0280 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03041 | hp2 | a0003 | c0006 | t0001 | g0298 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03098 | hp1 | a0001 | c0002 | t0008 | g0312 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03098 | hp2 | a0019 | c0031 | t0003 | g0252 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03130 | hp1 | a0003 | c0006 | t0002 | g0146 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03130 | hp2 | a0006 | c0007 | t0003 | g0150 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03139 | hp1 | a0002 | c0001 | t0002 | g0128 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03139 | hp2 | a0012 | c0013 | t0022 | g0178 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03209 | hp1 | a0003 | c0005 | t0007 | g0014 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0311 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03225 | hp1 | a0001 | c0004 | t0004 | g0251 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03225 | hp2 | a0015 | c0017 | t0002 | g0043 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03453 | hp1 | a0020 | c0026 | t0004 | g0363 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03453 | hp2 | a0002 | c0001 | t0002 | g0044 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03486 | hp2 | a0005 | c0010 | t0004 | g0175 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03490 | hp1 | a0001 | c0004 | t0013 | g0322 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03490 | hp2 | a0006 | c0007 | t0003 | g0002 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03491 | hp1 | a0004 | c0003 | t0021 | g0349 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03491 | hp2 | a0005 | c0008 | t0003 | g0258 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03492 | hp1 | a0005 | c0008 | t0003 | g0256 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03492 | hp2 | a0006 | c0007 | t0003 | g0002 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03516 | hp1 | a0002 | c0001 | t0006 | g0303 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03516 | hp2 | a0003 | c0006 | t0002 | g0167 | AFR | ESN | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0126 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03540 | hp2 | a0003 | c0005 | t0006 | g0253 | AFR | GWD | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03579 | hp1 | a0008 | c0011 | t0002 | g0190 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03579 | hp2 | a0003 | c0005 | t0002 | g0090 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03669 | hp1 | a0007 | c0009 | t0001 | g0053 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03669 | hp2 | a0002 | c0001 | t0002 | g0059 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03704 | hp1 | a0016 | c0021 | t0005 | g0346 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03704 | hp2 | a0002 | c0001 | t0002 | g0240 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0142 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03710 | hp2 | a0003 | c0005 | t0002 | g0004 | SAS | PJL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03831 | hp1 | a0001 | c0002 | t0004 | g0360 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03831 | hp2 | a0004 | c0003 | t0020 | g0026 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0095 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03834 | hp2 | a0004 | c0003 | t0001 | g0352 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0347 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03927 | hp2 | a0005 | c0010 | t0004 | g0257 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03942 | hp1 | a0004 | c0003 | t0005 | g0070 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03942 | hp2 | a0002 | c0001 | t0002 | g0036 | SAS | BEB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0328 | SAS | STU | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG04115 | hp2 | a0016 | c0021 | t0005 | g0362 | SAS | STU | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG04199 | hp1 | a0001 | c0004 | t0023 | g0188 | SAS | STU | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG04199 | hp2 | a0004 | c0003 | t0001 | g0228 | SAS | STU | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG04228 | hp1 | a0021 | c0029 | t0004 | g0321 | SAS | STU | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0133 | SAS | STU | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18522 | hp1 | a0001 | c0004 | t0004 | g0310 | AFR | YRI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18522 | hp2 | a0001 | c0004 | t0004 | g0127 | AFR | YRI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18612 | hp1 | a0002 | c0001 | t0002 | g0009 | EAS | CHB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18612 | hp2 | a0011 | c0015 | t0003 | g0055 | EAS | CHB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18747 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | CHB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | CHB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18906 | hp1 | a0022 | c0027 | t0009 | g0187 | AFR | YRI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18906 | hp2 | a0015 | c0017 | t0002 | g0254 | AFR | YRI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18939 | hp1 | a0004 | c0003 | t0001 | g0371 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18940 | hp2 | a0008 | c0011 | t0010 | g0194 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18941 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18941 | hp2 | a0002 | c0001 | t0002 | g0063 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0083 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0296 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18945 | hp2 | a0001 | c0004 | t0004 | g0320 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18946 | hp1 | a0003 | c0005 | t0001 | g0379 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18947 | hp1 | a0004 | c0003 | t0001 | g0124 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18947 | hp2 | a0013 | c0016 | t0001 | g0238 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18948 | hp1 | a0002 | c0001 | t0002 | g0034 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0086 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0304 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0327 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18952 | hp2 | a0002 | c0001 | t0005 | g0006 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18953 | hp1 | a0001 | c0004 | t0004 | g0118 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18953 | hp2 | a0004 | c0003 | t0001 | g0155 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18954 | hp1 | a0005 | c0010 | t0004 | g0237 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18954 | hp2 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18956 | hp1 | a0002 | c0001 | t0002 | g0319 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18956 | hp2 | a0002 | c0001 | t0005 | g0266 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18957 | hp1 | a0003 | c0005 | t0001 | g0116 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18957 | hp2 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18959 | hp1 | a0002 | c0001 | t0002 | g0102 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18961 | hp1 | a0004 | c0003 | t0001 | g0088 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0301 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18962 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18963 | hp1 | a0010 | c0014 | t0001 | g0216 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18963 | hp2 | a0002 | c0001 | t0002 | g0069 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18964 | hp1 | a0011 | c0015 | t0003 | g0284 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18964 | hp2 | a0003 | c0005 | t0001 | g0152 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18965 | hp1 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18965 | hp2 | a0003 | c0005 | t0001 | g0091 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18966 | hp1 | a0001 | c0004 | t0004 | g0369 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18969 | hp1 | a0007 | c0009 | t0001 | g0109 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18969 | hp2 | a0003 | c0006 | t0012 | g0365 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18970 | hp1 | a0002 | c0001 | t0002 | g0326 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18970 | hp2 | a0003 | c0005 | t0001 | g0072 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18972 | hp1 | a0005 | c0008 | t0003 | g0212 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0342 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18974 | hp1 | a0004 | c0019 | t0001 | g0265 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18974 | hp2 | a0008 | c0011 | t0010 | g0195 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18977 | hp1 | a0007 | c0009 | t0001 | g0008 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18977 | hp2 | a0004 | c0003 | t0001 | g0270 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18979 | hp1 | a0007 | c0009 | t0001 | g0244 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18979 | hp2 | a0002 | c0001 | t0005 | g0039 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18980 | hp1 | a0001 | c0004 | t0004 | g0367 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18980 | hp2 | a0007 | c0009 | t0001 | g0008 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18981 | hp2 | a0010 | c0014 | t0001 | g0192 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18982 | hp1 | a0004 | c0003 | t0001 | g0082 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18982 | hp2 | a0005 | c0008 | t0003 | g0207 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18983 | hp2 | a0005 | c0008 | t0003 | g0208 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18984 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18984 | hp2 | a0001 | c0004 | t0004 | g0107 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18985 | hp1 | a0008 | c0011 | t0005 | g0199 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18985 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18986 | hp1 | a0002 | c0001 | t0005 | g0112 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18988 | hp2 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0293 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18989 | hp2 | a0004 | c0003 | t0001 | g0011 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18991 | hp1 | a0005 | c0008 | t0003 | g0181 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18991 | hp2 | a0013 | c0016 | t0001 | g0230 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18993 | hp1 | a0010 | c0024 | t0001 | g0182 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18993 | hp2 | a0001 | c0004 | t0004 | g0364 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18994 | hp1 | a0004 | c0003 | t0001 | g0271 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18994 | hp2 | a0002 | c0001 | t0002 | g0245 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18997 | hp1 | a0010 | c0014 | t0001 | g0179 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18997 | hp2 | a0002 | c0001 | t0002 | g0060 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18999 | hp1 | a0002 | c0001 | t0002 | g0032 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0269 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19000 | hp1 | a0003 | c0005 | t0002 | g0038 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19003 | hp2 | a0001 | c0004 | t0004 | g0373 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19004 | hp1 | a0005 | c0008 | t0003 | g0215 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19004 | hp2 | a0001 | c0004 | t0004 | g0366 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19005 | hp1 | a0005 | c0008 | t0003 | g0219 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19005 | hp2 | a0023 | c0032 | t0002 | g0331 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19009 | hp1 | a0004 | c0003 | t0001 | g0156 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19011 | hp1 | a0002 | c0001 | t0005 | g0247 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19012 | hp1 | a0004 | c0003 | t0001 | g0122 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19012 | hp2 | a0007 | c0009 | t0001 | g0246 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19030 | hp1 | a0024 | c0034 | t0009 | g0191 | AFR | LWK | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19030 | hp2 | a0002 | c0001 | t0002 | g0268 | AFR | LWK | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19043 | hp1 | a0003 | c0005 | t0007 | g0014 | AFR | LWK | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19043 | hp2 | a0003 | c0005 | t0017 | g0144 | AFR | LWK | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19056 | hp1 | a0002 | c0001 | t0002 | g0062 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19056 | hp2 | a0003 | c0006 | t0012 | g0370 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19057 | hp1 | a0003 | c0005 | t0002 | g0325 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19057 | hp2 | a0007 | c0009 | t0001 | g0022 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19058 | hp1 | a0009 | c0012 | t0005 | g0222 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19058 | hp2 | a0004 | c0003 | t0001 | g0232 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19060 | hp2 | a0004 | c0003 | t0001 | g0272 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19062 | hp1 | a0002 | c0001 | t0019 | g0041 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19062 | hp2 | a0005 | c0008 | t0003 | g0211 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19063 | hp1 | a0004 | c0003 | t0001 | g0077 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19063 | hp2 | a0013 | c0016 | t0001 | g0180 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19064 | hp1 | a0005 | c0008 | t0003 | g0214 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19064 | hp2 | a0002 | c0001 | t0005 | g0006 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19066 | hp1 | a0002 | c0001 | t0005 | g0006 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19066 | hp2 | a0009 | c0012 | t0005 | g0220 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19068 | hp1 | a0002 | c0001 | t0002 | g0050 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19068 | hp2 | a0005 | c0008 | t0003 | g0209 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19072 | hp1 | a0009 | c0012 | t0002 | g0236 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19072 | hp2 | a0003 | c0005 | t0001 | g0119 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19080 | hp1 | a0002 | c0001 | t0005 | g0100 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19080 | hp2 | a0005 | c0008 | t0003 | g0218 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19081 | hp1 | a0003 | c0005 | t0005 | g0372 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19081 | hp2 | a0012 | c0013 | t0003 | g0204 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19083 | hp1 | a0002 | c0001 | t0005 | g0033 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19083 | hp2 | a0005 | c0010 | t0013 | g0205 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19084 | hp1 | a0004 | c0003 | t0001 | g0302 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19084 | hp2 | a0003 | c0005 | t0002 | g0330 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19085 | hp1 | a0004 | c0003 | t0001 | g0151 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19085 | hp2 | a0007 | c0009 | t0001 | g0105 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0037 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19086 | hp2 | a0002 | c0001 | t0002 | g0104 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19087 | hp1 | a0004 | c0003 | t0001 | g0123 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0377 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19088 | hp2 | a0009 | c0012 | t0002 | g0206 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19090 | hp1 | a0006 | c0007 | t0003 | g0056 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19091 | hp1 | a0004 | c0003 | t0001 | g0157 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19240 | hp1 | a0004 | c0003 | t0001 | g0131 | AFR | YRI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA19240 | hp2 | a0002 | c0001 | t0002 | g0380 | AFR | YRI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20129 | hp1 | a0005 | c0008 | t0004 | g0171 | AFR | ASW | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0110 | AFR | ASW | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20752 | hp1 | a0025 | c0030 | t0004 | g0262 | EUR | TSI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20752 | hp2 | a0003 | c0006 | t0002 | g0141 | EUR | TSI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20805 | hp1 | a0004 | c0003 | t0001 | g0154 | EUR | TSI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20805 | hp2 | a0002 | c0001 | t0002 | g0035 | EUR | TSI | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20905 | hp1 | a0013 | c0016 | t0001 | g0198 | SAS | GIH | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA20905 | hp2 | a0006 | c0007 | t0004 | g0163 | SAS | GIH | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02109 | hp1 | a0002 | c0001 | t0002 | g0356 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02109 | hp2 | a0008 | c0011 | t0002 | g0173 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02486 | hp1 | a0008 | c0011 | t0001 | g0172 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02486 | hp2 | a0001 | c0004 | t0016 | g0259 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02559 | hp1 | a0002 | c0001 | t0002 | g0046 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG02559 | hp2 | a0003 | c0006 | t0002 | g0121 | AFR | ACB | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03471 | hp1 | a0005 | c0010 | t0004 | g0177 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG03471 | hp2 | a0002 | c0001 | t0002 | g0047 | AFR | MSL | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG06807 | hp1 | a0001 | c0004 | t0004 | g0348 | AFR | USA | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| HG06807 | hp2 | a0002 | c0001 | t0002 | g0113 | AFR | USA | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18955 | hp1 | a0002 | c0001 | t0005 | g0061 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0018 | g0381 | REF | REF | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| homoSapiens | grch38p0 | a0008 | c0011 | t0002 | g0189 | REF | REF | SLC14A2_chr18_45610476_45688688 | SLC14A2 | chr18 | 45610476 | 45688688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45624774 | C | T | 1 | a0017 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.110C>T | p.Thr37Ile | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/20 | 251/4073 | 110/2763 | 37/920 | chr18 | 45624774 | |||
| chr18:45627020 | A | G | 19 | a0001 a0002 a0003 others(16): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
missense_variant | MODERATE | c.394A>G | p.Ile132Val | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/20 | 535/4073 | 394/2763 | 132/920 | chr18 | 45627020 | |||
| chr18:45643140 | T | C | 2 | a0020 a0022 |
2 | HG03453.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1135T>C | p.Cys379Arg | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 9/20 | 1276/4073 | 1135/2763 | 379/920 | chr18 | 45643140 | |||
| chr18:45644136 | G | A | 1 | a0015 | 3 | HG02965.hp2 HG03225.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1327G>A | p.Gly443Ser | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/20 | 1468/4073 | 1327/2763 | 443/920 | chr18 | 45644136 | |||
| chr18:45644160 | G | A | 1 | a0018 | 1 | HG02809.hp1 | missense_variant&splice_region_variant | MODERATE | c.1351G>A | p.Gly451Arg | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/20 | 1492/4073 | 1351/2763 | 451/920 | chr18 | 45644160 | |||
| chr18:45666191 | G | A | 10 | a0002 a0006 a0007 others(7): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
missense_variant | MODERATE | c.1529G>A | p.Arg510Gln | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/20 | 1670/4073 | 1529/2763 | 510/920 | chr18 | 45666191 | |||
| chr18:45667868 | C | T | 1 | a0024 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.1753C>T | p.Leu585Phe | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 14/20 | 1894/4073 | 1753/2763 | 585/920 | chr18 | 45667868 | |||
| chr18:45672918 | G | A | 6 | a0004 a0007 a0010 others(3): Show |
84 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
missense_variant | MODERATE | c.2248G>A | p.Val750Ile | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/20 | 2389/4073 | 2248/2763 | 750/920 | chr18 | 45672918 | |||
| chr18:45672939 | G | A | 1 | a0016 | 2 | HG03704.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.2269G>A | p.Gly757Ser | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/20 | 2410/4073 | 2269/2763 | 757/920 | chr18 | 45672939 | |||
| chr18:45673794 | C | T | 2 | a0019 a0023 |
2 | HG03098.hp2 NA19005.hp2 |
missense_variant | MODERATE | c.2489C>T | p.Thr830Met | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/20 | 2630/4073 | 2489/2763 | 830/920 | chr18 | 45673794 | |||
| chr18:45682394 | G | A | 10 | a0001 a0005 a0006 others(7): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
missense_variant | MODERATE | c.2638G>A | p.Ala880Thr | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 2779/4073 | 2638/2763 | 880/920 | chr18 | 45682394 | |||
| chr18:45682443 | G | A | 2 | a0014 a0025 |
4 | HG01243.hp2 HG02015.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.2687G>A | p.Arg896His | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 2828/4073 | 2687/2763 | 896/920 | chr18 | 45682443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45624769 | G | A | 1 | a0001c0023 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.105G>A | p.Pro35Pro | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/20 | 246/4073 | 105/2763 | 35/920 | chr18 | 45624769 | |||
| chr18:45627004 | C | T | 1 | a0009c0035 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.378C>T | p.Thr126Thr | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/20 | 519/4073 | 378/2763 | 126/920 | chr18 | 45627004 | |||
| chr18:45663837 | G | A | 1 | a0003c0018 | 3 | HG01070.hp2 HG01071.hp2 HG01516.hp1 |
synonymous_variant | LOW | c.1404G>A | p.Ser468Ser | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/20 | 1545/4073 | 1404/2763 | 468/920 | chr18 | 45663837 | |||
| chr18:45667036 | C | G | 24 | a0001c0004 a0001c0022 a0001c0023 others(21): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
synonymous_variant | LOW | c.1659C>G | p.Val553Val | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/20 | 1800/4073 | 1659/2763 | 553/920 | chr18 | 45667036 | |||
| chr18:45668379 | C | T | 1 | a0003c0033 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1938C>T | p.Tyr646Tyr | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/20 | 2079/4073 | 1938/2763 | 646/920 | chr18 | 45668379 | |||
| chr18:45682483 | A | C | 1 | a0001c0022 | 2 | HG01192.hp1 HG02145.hp1 |
synonymous_variant | LOW | c.2727A>C | p.Ser909Ser | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 2868/4073 | 2727/2763 | 909/920 | chr18 | 45682483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45615504 | G | A | 1 | a0002c0001t0015 | 1 | HG01070.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/20 | 9161 | chr18 | 45615504 | ||||||
| chr18:45615547 | G | A | 1 | a0001c0004t0016 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/20 | 9118 | chr18 | 45615547 | ||||||
| chr18:45682536 | C | T | 27 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0008 others(24): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*17C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 17 | chr18 | 45682536 | ||||||
| chr18:45682546 | T | C | 2 | a0003c0005t0007 a0003c0005t0017 |
7 | HG02630.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*27T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 27 | chr18 | 45682546 | ||||||
| chr18:45682567 | C | A | 33 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0008 others(30): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*48C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 48 | chr18 | 45682567 | ||||||
| chr18:45682568 | G | A | 1 | a0008c0011t0010 | 2 | NA18940.hp2 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 49 | chr18 | 45682568 | ||||||
| chr18:45682699 | A | T | 13 | a0002c0001t0001 a0003c0005t0001 a0003c0006t0001 others(10): Show |
103 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*180A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 180 | chr18 | 45682699 | ||||||
| chr18:45683017 | C | A | 1 | a0001c0002t0008 | 6 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 498 | chr18 | 45683017 | ||||||
| chr18:45683028 | A | C | 7 | a0002c0001t0005 a0002c0001t0019 a0003c0005t0005 others(4): Show |
24 | HG00438.hp1 HG00733.hp2 HG01192.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*509A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 509 | chr18 | 45683028 | ||||||
| chr18:45683093 | C | CA | 10 | a0001c0004t0013 a0001c0004t0016 a0002c0001t0006 others(7): Show |
15 | HG00741.hp2 HG01109.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*588dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 589 | INFO_REALIGN_3_PRIME | chr18 | 45683093 | |||||
| chr18:45683107 | AG | A | 14 | a0002c0001t0001 a0003c0005t0001 a0003c0006t0001 others(11): Show |
104 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*592delG | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 592 | INFO_REALIGN_3_PRIME | chr18 | 45683107 | |||||
| chr18:45683108 | G | A | 49 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0008 others(46): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*589G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 589 | chr18 | 45683108 | ||||||
| chr18:45683135 | G | T | 13 | a0002c0001t0001 a0003c0005t0001 a0003c0006t0001 others(10): Show |
103 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*616G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 616 | chr18 | 45683135 | ||||||
| chr18:45683260 | A | G | 1 | a0001c0004t0023 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 741 | chr18 | 45683260 | ||||||
| chr18:45683285 | C | G | 2 | a0001c0004t0016 a0005c0010t0014 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*766C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 766 | chr18 | 45683285 | ||||||
| chr18:45683304 | A | C | 1 | a0003c0006t0012 | 2 | NA18969.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*785A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 785 | chr18 | 45683304 | ||||||
| chr18:45683321 | G | A | 10 | a0001c0002t0003 a0001c0004t0003 a0001c0023t0003 others(7): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*802G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 802 | chr18 | 45683321 | ||||||
| chr18:45683380 | T | C | 1 | a0004c0003t0020 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*861T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 861 | chr18 | 45683380 | ||||||
| chr18:45683397 | G | A | 1 | a0003c0005t0007 | 6 | HG02630.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*878G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 878 | chr18 | 45683397 | ||||||
| chr18:45683471 | T | C | 1 | a0004c0003t0021 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 20/20 | 952 | chr18 | 45683471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45615600 | C | CT | 113 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(110): Show |
115 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-35+32dupT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615600 | ||||||
| chr18:45615600 | CT | C | 7 | a0001c0002t0003g0010 a0001c0002t0003g0168 a0001c0004t0004g0020 others(4): Show |
7 | HG00733.hp1 HG02258.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35+32delT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615600 | ||||||
| chr18:45615618 | A | G | 1 | a0002c0001t0002g0380 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-35+36A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615618 | |||||||
| chr18:45615713 | A | C | 1 | a0003c0005t0001g0379 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-35+131A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615713 | |||||||
| chr18:45615817 | A | ATG | 92 | a0001c0002t0003g0283 a0001c0002t0003g0293 a0001c0002t0003g0294 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-35+254_-35+255dup others(2): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615817 | ||||||
| chr18:45615817 | A | ATGTG | 4 | a0001c0002t0003g0377 a0001c0002t0004g0376 a0001c0023t0003g0374 others(1): Show |
4 | HG02129.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+252_-35+255dup others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615817 | ||||||
| chr18:45615836 | T | TGTGA | 4 | a0001c0002t0003g0269 a0004c0003t0001g0270 a0004c0003t0001g0271 others(1): Show |
4 | NA18977.hp2 NA18994.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+255_-35+256ins others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615836 | ||||||
| chr18:45615836 | T | TGTGAGA | 3 | a0002c0001t0002g0268 a0003c0005t0007g0014 a0003c0005t0007g0267 |
4 | HG02647.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+255_-35+256ins others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615836 | ||||||
| chr18:45615836 | T | TGTGTGAG others(1): Show |
10 | a0001c0004t0004g0364 a0001c0004t0004g0366 a0001c0004t0004g0367 others(7): Show |
10 | HG01928.hp2 NA18939.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+255_-35+256ins others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615836 | ||||||
| chr18:45615836 | TGA | T | 15 | a0001c0002t0003g0005 a0001c0002t0003g0248 a0001c0002t0003g0250 others(12): Show |
17 | HG01496.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-35+276_-35+277del others(2): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615836 | ||||||
| chr18:45615836 | TGAGAGA | T | 4 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0003c0006t0002g0263 others(1): Show |
4 | HG00099.hp2 HG00741.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+272_-35+277del others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615836 | ||||||
| chr18:45615836 | TGAGAGAG others(5): Show |
T | 2 | a0004c0019t0001g0264 a0004c0019t0001g0265 |
2 | HG00673.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-35+266_-35+277del others(12): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45615836 | ||||||
| chr18:45615838 | A | T | 169 | a0001c0002t0003g0007 a0001c0002t0003g0017 a0001c0002t0003g0031 others(166): Show |
181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.-35+256A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615838 | |||||||
| chr18:45615840 | A | T | 4 | a0002c0001t0002g0378 a0002c0001t0002g0380 a0002c0001t0005g0006 others(1): Show |
6 | HG02970.hp1 NA18952.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+258A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615840 | |||||||
| chr18:45615842 | A | T | 1 | a0002c0001t0002g0378 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-35+260A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615842 | |||||||
| chr18:45615900 | A | G | 1 | a0001c0004t0016g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-35+318A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615900 | |||||||
| chr18:45615923 | T | A | 10 | a0001c0004t0004g0276 a0001c0004t0004g0277 a0001c0004t0004g0278 others(7): Show |
10 | HG01071.hp1 HG01081.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+341T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615923 | |||||||
| chr18:45615980 | G | A | 6 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+398G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45615980 | |||||||
| chr18:45616058 | C | T | 1 | a0020c0026t0004g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-35+476C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616058 | |||||||
| chr18:45616137 | G | A | 2 | a0001c0002t0003g0283 a0011c0015t0003g0284 |
2 | HG02080.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-35+555G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616137 | |||||||
| chr18:45616174 | T | A | 3 | a0001c0002t0003g0283 a0002c0001t0001g0285 a0011c0015t0003g0284 |
3 | HG02074.hp2 HG02080.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-35+592T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616174 | |||||||
| chr18:45616200 | A | G | 1 | a0016c0021t0005g0362 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-35+618A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616200 | |||||||
| chr18:45616387 | T | C | 21 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(18): Show |
23 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-35+805T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616387 | |||||||
| chr18:45616399 | C | A | 2 | a0002c0001t0002g0018 a0002c0001t0002g0019 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-35+817C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616399 | |||||||
| chr18:45616473 | G | A | 1 | a0002c0001t0002g0378 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-35+891G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616473 | |||||||
| chr18:45616476 | G | A | 1 | a0002c0001t0002g0380 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-35+894G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616476 | |||||||
| chr18:45616639 | T | C | 125 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(122): Show |
128 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-35+1057T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616639 | |||||||
| chr18:45616844 | T | C | 3 | a0001c0023t0003g0374 a0002c0001t0002g0286 a0002c0001t0002g0287 |
3 | HG01167.hp1 HG01169.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-35+1262T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45616844 | |||||||
| chr18:45617496 | C | G | 11 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0001c0023t0003g0374 others(8): Show |
11 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35+1914C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617496 | |||||||
| chr18:45617526 | C | G | 5 | a0002c0001t0002g0245 a0002c0001t0005g0247 a0007c0009t0001g0001 others(2): Show |
8 | HG01257.hp1 NA18954.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+1944C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617526 | |||||||
| chr18:45617612 | C | T | 6 | a0001c0002t0003g0355 a0001c0002t0003g0377 a0002c0001t0002g0380 others(3): Show |
6 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+2030C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617612 | |||||||
| chr18:45617716 | G | C | 1 | a0001c0004t0004g0020 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-35+2134G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617716 | |||||||
| chr18:45617733 | T | C | 3 | a0001c0023t0003g0374 a0002c0001t0002g0286 a0002c0001t0002g0287 |
3 | HG01167.hp1 HG01169.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-35+2151T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617733 | |||||||
| chr18:45617814 | C | T | 10 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(7): Show |
12 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+2232C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617814 | |||||||
| chr18:45617920 | G | C | 1 | a0011c0015t0004g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-35+2338G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45617920 | |||||||
| chr18:45618033 | G | A | 1 | a0017c0036t0002g0288 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-35+2451G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618033 | |||||||
| chr18:45618140 | A | G | 1 | a0006c0007t0003g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-35+2558A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618140 | |||||||
| chr18:45618176 | T | C | 178 | a0001c0002t0003g0007 a0001c0002t0003g0010 a0001c0002t0003g0031 others(175): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.-35+2594T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618176 | |||||||
| chr18:45618353 | T | C | 120 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(117): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-35+2771T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618353 | |||||||
| chr18:45618669 | C | CA | 33 | a0001c0002t0003g0031 a0001c0004t0004g0186 a0002c0001t0001g0025 others(30): Show |
35 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-35+3116dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45618669 | ||||||
| chr18:45618669 | CA | C | 58 | a0001c0002t0003g0017 a0001c0002t0003g0110 a0001c0002t0003g0115 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-35+3116delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45618669 | ||||||
| chr18:45618669 | CAA | C | 66 | a0001c0002t0003g0005 a0001c0002t0003g0250 a0001c0002t0003g0327 others(63): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-35+3115_-35+3116d others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45618669 | ||||||
| chr18:45618669 | CAAA | C | 8 | a0001c0002t0003g0355 a0001c0002t0004g0242 a0001c0004t0004g0282 others(5): Show |
8 | HG00621.hp1 HG01496.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+3114_-35+3116d others(5): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45618669 | ||||||
| chr18:45618669 | CAAAAAAA others(2): Show |
C | 53 | a0001c0002t0003g0010 a0001c0002t0003g0133 a0001c0002t0003g0361 others(50): Show |
57 | HG00140.hp2 HG00544.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35+3108_-35+3116d others(11): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45618669 | ||||||
| chr18:45618669 | CAAAAAAA others(3): Show |
C | 5 | a0001c0002t0003g0168 a0002c0001t0006g0166 a0003c0006t0002g0165 others(2): Show |
5 | HG01975.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+3107_-35+3116d others(12): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr18 | 45618669 | ||||||
| chr18:45618673 | A | C | 1 | a0020c0026t0004g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-35+3091A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618673 | |||||||
| chr18:45618696 | A | C | 10 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(7): Show |
12 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+3114A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618696 | |||||||
| chr18:45618696 | A | G | 1 | a0001c0002t0008g0350 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+3114A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618696 | |||||||
| chr18:45618828 | T | A | 1 | a0001c0004t0023g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-35+3246T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45618828 | |||||||
| chr18:45619062 | T | G | 1 | a0014c0020t0004g0274 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-35+3480T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619062 | |||||||
| chr18:45619073 | C | T | 14 | a0001c0002t0003g0099 a0001c0002t0003g0101 a0001c0002t0003g0106 others(11): Show |
15 | HG02056.hp2 HG02155.hp2 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.-35+3491C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619073 | |||||||
| chr18:45619290 | C | G | 1 | a0002c0001t0005g0033 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-35+3708C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619290 | |||||||
| chr18:45619304 | C | T | 2 | a0002c0001t0002g0286 a0002c0001t0002g0287 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-35+3722C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619304 | |||||||
| chr18:45619332 | G | A | 6 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+3750G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619332 | |||||||
| chr18:45619443 | A | C | 6 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+3861A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619443 | |||||||
| chr18:45619875 | C | G | 3 | a0002c0001t0002g0286 a0002c0001t0002g0287 a0002c0001t0002g0378 |
3 | HG01167.hp1 HG01169.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-35+4293C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45619875 | |||||||
| chr18:45620026 | C | T | 1 | a0001c0004t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-35+4444C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620026 | |||||||
| chr18:45620050 | A | T | 11 | a0001c0002t0003g0092 a0001c0002t0003g0097 a0002c0001t0001g0095 others(8): Show |
13 | HG00673.hp1 HG02015.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-35+4468A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620050 | |||||||
| chr18:45620097 | T | C | 117 | a0001c0002t0003g0007 a0001c0002t0003g0031 a0001c0002t0003g0040 others(114): Show |
129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-35+4515T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620097 | |||||||
| chr18:45620173 | A | T | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-34-4458A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620173 | |||||||
| chr18:45620185 | A | C | 319 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(316): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-4446A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620185 | |||||||
| chr18:45620431 | G | A | 1 | a0001c0002t0008g0249 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-34-4200G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620431 | |||||||
| chr18:45620463 | C | G | 1 | a0002c0001t0001g0089 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-34-4168C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620463 | |||||||
| chr18:45620647 | T | C | 14 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(11): Show |
17 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34-3984T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620647 | |||||||
| chr18:45620654 | C | A | 2 | a0003c0005t0002g0297 a0004c0003t0001g0292 |
2 | HG01074.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-34-3977C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620654 | |||||||
| chr18:45620675 | C | T | 1 | a0004c0003t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-34-3956C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620675 | |||||||
| chr18:45620688 | C | T | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-34-3943C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45620688 | |||||||
| chr18:45621060 | G | A | 1 | a0002c0001t0002g0034 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-34-3571G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45621060 | |||||||
| chr18:45621176 | T | C | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-34-3455T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45621176 | |||||||
| chr18:45621204 | C | G | 1 | a0001c0004t0004g0348 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-34-3427C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45621204 | |||||||
| chr18:45621445 | G | A | 7 | a0005c0008t0004g0171 a0005c0010t0004g0175 a0005c0010t0004g0176 others(4): Show |
7 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-3186G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45621445 | |||||||
| chr18:45621578 | G | A | 2 | a0002c0001t0002g0286 a0002c0001t0002g0287 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-34-3053G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45621578 | |||||||
| chr18:45621648 | G | A | 52 | a0001c0002t0003g0327 a0001c0002t0003g0328 a0001c0002t0003g0332 others(49): Show |
52 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-2983G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45621648 | |||||||
| chr18:45622011 | G | A | 1 | a0010c0014t0001g0192 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-34-2620G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622011 | |||||||
| chr18:45622081 | C | T | 3 | a0001c0002t0004g0086 a0001c0002t0004g0087 a0007c0009t0001g0008 |
4 | NA18948.hp2 NA18951.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-2550C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622081 | |||||||
| chr18:45622106 | A | T | 20 | a0001c0002t0003g0361 a0001c0002t0004g0360 a0002c0001t0005g0153 others(17): Show |
22 | HG00140.hp2 HG00673.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-2525A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622106 | |||||||
| chr18:45622109 | G | T | 3 | a0001c0002t0003g0168 a0003c0005t0001g0152 a0004c0003t0001g0151 |
3 | NA18964.hp2 NA19003.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-34-2522G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622109 | |||||||
| chr18:45622118 | T | G | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-34-2513T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622118 | |||||||
| chr18:45622146 | G | A | 7 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-2485G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622146 | |||||||
| chr18:45622439 | C | T | 306 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(303): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.-34-2192C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622439 | |||||||
| chr18:45622449 | G | A | 1 | a0001c0004t0016g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-34-2182G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622449 | |||||||
| chr18:45622535 | G | A | 1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-34-2096G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622535 | |||||||
| chr18:45622613 | G | A | 1 | a0004c0003t0001g0352 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-34-2018G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622613 | |||||||
| chr18:45622626 | G | C | 1 | a0002c0001t0002g0378 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-34-2005G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622626 | |||||||
| chr18:45622700 | A | G | 1 | a0002c0001t0002g0380 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-1931A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622700 | |||||||
| chr18:45622754 | G | A | 1 | a0003c0006t0002g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-34-1877G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45622754 | |||||||
| chr18:45623136 | G | A | 1 | a0004c0003t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-34-1495G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623136 | |||||||
| chr18:45623627 | T | A | 86 | a0001c0002t0003g0005 a0001c0002t0003g0010 a0001c0002t0003g0017 others(83): Show |
93 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-34-1004T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623627 | |||||||
| chr18:45623740 | G | A | 15 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(12): Show |
18 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-34-891G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623740 | |||||||
| chr18:45623784 | C | A | 2 | a0011c0015t0004g0299 a0011c0015t0004g0300 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-34-847C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623784 | |||||||
| chr18:45623792 | A | G | 2 | a0002c0001t0002g0286 a0002c0001t0002g0287 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-34-839A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623792 | |||||||
| chr18:45623820 | C | T | 85 | a0001c0002t0003g0005 a0001c0002t0003g0010 a0001c0002t0003g0017 others(82): Show |
92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-34-811C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623820 | |||||||
| chr18:45623895 | A | G | 7 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-736A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623895 | |||||||
| chr18:45623926 | G | A | 1 | a0004c0003t0001g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-34-705G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623926 | |||||||
| chr18:45623964 | A | G | 1 | a0003c0006t0002g0233 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34-667A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45623964 | |||||||
| chr18:45624163 | A | G | 1 | a0001c0002t0004g0242 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-34-468A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624163 | |||||||
| chr18:45624291 | G | A | 74 | a0001c0002t0003g0005 a0001c0002t0003g0010 a0001c0002t0003g0017 others(71): Show |
81 | HG00140.hp2 HG00544.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.-34-340G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624291 | |||||||
| chr18:45624306 | C | T | 4 | a0002c0001t0001g0083 a0002c0001t0001g0084 a0002c0001t0001g0085 others(1): Show |
4 | NA18941.hp1 NA18944.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-325C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624306 | |||||||
| chr18:45624312 | T | C | 1 | a0003c0006t0002g0121 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-34-319T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624312 | |||||||
| chr18:45624441 | G | A | 1 | a0001c0002t0003g0250 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-34-190G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624441 | |||||||
| chr18:45624592 | G | A | 1 | a0002c0001t0002g0035 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-34-39G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624592 | |||||||
| chr18:45624625 | G | A | 2 | a0001c0004t0023g0188 a0004c0003t0001g0270 |
2 | HG04199.hp1 NA18977.hp2 |
splice_region_variant&intron_variant | LOW | c.-34-6G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 1/19 | chr18 | 45624625 | |||||||
| chr18:45624883 | C | T | 6 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+69C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45624883 | |||||||
| chr18:45624903 | G | C | 2 | a0002c0001t0002g0018 a0002c0001t0002g0019 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.150+89G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45624903 | |||||||
| chr18:45624994 | G | A | 1 | a0002c0001t0002g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.150+180G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45624994 | |||||||
| chr18:45625253 | C | T | 1 | a0004c0003t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.151-430C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45625253 | |||||||
| chr18:45625259 | C | A | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.151-424C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45625259 | |||||||
| chr18:45625408 | T | C | 2 | a0001c0002t0003g0168 a0003c0005t0001g0152 |
2 | NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.151-275T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45625408 | |||||||
| chr18:45625425 | T | C | 6 | a0001c0002t0003g0010 a0004c0003t0001g0011 a0004c0003t0001g0120 others(3): Show |
8 | HG00544.hp2 HG02129.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.151-258T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45625425 | |||||||
| chr18:45625665 | G | A | 7 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-18G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 2/19 | chr18 | 45625665 | |||||||
| chr18:45626391 | T | C | 1 | a0002c0001t0002g0380 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.331+528T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 3/19 | chr18 | 45626391 | |||||||
| chr18:45626641 | CCCTTGGA others(5): Show |
C | 2 | a0005c0008t0004g0171 a0008c0011t0001g0172 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.332-314_332-303del others(12): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr18 | 45626641 | ||||||
| chr18:45626866 | A | T | 2 | a0004c0003t0001g0232 a0004c0003t0001g0291 |
2 | HG02040.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.332-92A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 3/19 | chr18 | 45626866 | |||||||
| chr18:45627267 | T | A | 1 | a0002c0001t0001g0083 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.521+120T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627267 | |||||||
| chr18:45627322 | G | A | 3 | a0001c0002t0003g0301 a0001c0002t0003g0345 a0004c0003t0001g0302 |
3 | NA18961.hp2 NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.521+175G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627322 | |||||||
| chr18:45627620 | G | A | 54 | a0001c0002t0003g0010 a0001c0002t0003g0110 a0001c0002t0003g0133 others(51): Show |
58 | HG00140.hp2 HG00544.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.521+473G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627620 | |||||||
| chr18:45627691 | G | A | 3 | a0001c0004t0004g0320 a0002c0001t0002g0319 a0003c0006t0002g0318 |
3 | HG00280.hp1 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.521+544G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627691 | |||||||
| chr18:45627743 | T | C | 1 | a0002c0001t0001g0037 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.521+596T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627743 | |||||||
| chr18:45627839 | G | A | 2 | a0001c0023t0003g0374 a0002c0001t0002g0380 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.521+692G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627839 | |||||||
| chr18:45627870 | C | T | 1 | a0003c0005t0001g0081 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.521+723C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45627870 | |||||||
| chr18:45628000 | C | CA | 18 | a0001c0002t0003g0040 a0001c0002t0003g0092 a0001c0002t0003g0283 others(15): Show |
19 | HG00423.hp1 HG00738.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.521+873dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628000 | ||||||
| chr18:45628000 | CA | C | 9 | a0001c0002t0004g0087 a0001c0004t0004g0098 a0001c0004t0004g0373 others(6): Show |
9 | HG00735.hp1 HG01168.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.521+873delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628000 | ||||||
| chr18:45628000 | CAAA | C | 65 | a0001c0002t0003g0010 a0001c0002t0003g0110 a0001c0002t0003g0133 others(62): Show |
69 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.521+871_521+873del others(3): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628000 | ||||||
| chr18:45628000 | CAAAA | C | 6 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.521+870_521+873del others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628000 | ||||||
| chr18:45628016 | A | G | 68 | a0001c0002t0003g0010 a0001c0002t0003g0110 a0001c0002t0003g0133 others(65): Show |
72 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.521+869A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628016 | |||||||
| chr18:45628021 | G | A | 21 | a0001c0002t0003g0283 a0001c0002t0003g0293 a0001c0002t0003g0294 others(18): Show |
21 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.521+874G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628021 | |||||||
| chr18:45628089 | G | A | 1 | a0001c0004t0004g0020 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.521+942G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628089 | |||||||
| chr18:45628305 | G | A | 1 | a0001c0002t0008g0350 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.521+1158G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628305 | |||||||
| chr18:45628360 | C | CT | 7 | a0001c0002t0004g0376 a0001c0023t0003g0374 a0002c0001t0002g0380 others(4): Show |
7 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+1215dupT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628360 | ||||||
| chr18:45628392 | C | T | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.521+1245C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628392 | |||||||
| chr18:45628399 | G | A | 1 | a0001c0004t0004g0310 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.521+1252G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628399 | |||||||
| chr18:45628400 | C | T | 1 | a0004c0003t0001g0302 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.521+1253C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628400 | |||||||
| chr18:45628442 | CA | C | 289 | a0001c0002t0003g0007 a0001c0002t0003g0010 a0001c0002t0003g0031 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.521+1312delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628442 | ||||||
| chr18:45628442 | CAA | C | 9 | a0001c0002t0004g0376 a0001c0023t0003g0374 a0002c0001t0001g0085 others(6): Show |
9 | HG00323.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.521+1311_521+1312d others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45628442 | ||||||
| chr18:45628478 | G | A | 95 | a0001c0002t0003g0054 a0001c0002t0003g0092 a0001c0002t0003g0099 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.521+1331G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628478 | |||||||
| chr18:45628694 | G | T | 3 | a0001c0002t0004g0242 a0001c0004t0016g0259 a0002c0001t0006g0080 |
3 | HG01109.hp2 HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.521+1547G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628694 | |||||||
| chr18:45628740 | G | A | 7 | a0001c0002t0004g0376 a0001c0023t0003g0374 a0002c0001t0002g0380 others(4): Show |
7 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+1593G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628740 | |||||||
| chr18:45628847 | C | G | 1 | a0006c0007t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.521+1700C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45628847 | |||||||
| chr18:45629037 | T | A | 6 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0002c0001t0002g0015 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.521+1890T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629037 | |||||||
| chr18:45629215 | C | T | 99 | a0001c0002t0003g0054 a0001c0002t0003g0092 a0001c0002t0003g0099 others(96): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.521+2068C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629215 | |||||||
| chr18:45629247 | TA | T | 4 | a0005c0010t0004g0175 a0005c0010t0004g0176 a0005c0010t0004g0177 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+2101delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629247 | |||||||
| chr18:45629256 | G | C | 3 | a0001c0002t0004g0242 a0001c0004t0016g0259 a0002c0001t0006g0080 |
3 | HG01109.hp2 HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.521+2109G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629256 | |||||||
| chr18:45629261 | A | T | 1 | a0004c0003t0005g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.521+2114A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629261 | |||||||
| chr18:45629419 | C | T | 91 | a0001c0002t0003g0007 a0001c0002t0003g0010 a0001c0002t0003g0031 others(88): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.521+2272C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629419 | |||||||
| chr18:45629459 | C | A | 1 | a0004c0003t0001g0302 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.521+2312C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629459 | |||||||
| chr18:45629621 | A | G | 1 | a0001c0002t0003g0108 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.521+2474A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629621 | |||||||
| chr18:45629645 | G | A | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.521+2498G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629645 | |||||||
| chr18:45629745 | G | A | 1 | a0003c0005t0002g0325 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.521+2598G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629745 | |||||||
| chr18:45629993 | C | A | 3 | a0001c0002t0004g0242 a0001c0004t0016g0259 a0002c0001t0006g0080 |
3 | HG01109.hp2 HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.522-2357C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45629993 | |||||||
| chr18:45630229 | G | A | 143 | a0001c0002t0003g0007 a0001c0002t0003g0010 a0001c0002t0003g0031 others(140): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.522-2121G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45630229 | |||||||
| chr18:45630288 | G | C | 1 | a0002c0001t0002g0378 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.522-2062G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45630288 | |||||||
| chr18:45630294 | C | T | 1 | a0003c0018t0002g0030 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.522-2056C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45630294 | |||||||
| chr18:45630337 | A | G | 1 | a0002c0001t0001g0347 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.522-2013A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45630337 | |||||||
| chr18:45630657 | A | G | 1 | a0006c0007t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.522-1693A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45630657 | |||||||
| chr18:45630914 | G | A | 9 | a0002c0001t0002g0023 a0002c0001t0002g0044 a0002c0001t0002g0046 others(6): Show |
9 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.522-1436G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45630914 | |||||||
| chr18:45631035 | C | G | 2 | a0001c0002t0008g0249 a0001c0002t0008g0255 |
2 | HG01496.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.522-1315C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631035 | |||||||
| chr18:45631151 | C | T | 3 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0002c0001t0006g0080 |
3 | HG01109.hp2 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.522-1199C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631151 | |||||||
| chr18:45631355 | C | T | 45 | a0001c0002t0003g0007 a0001c0002t0003g0031 a0001c0002t0003g0040 others(42): Show |
47 | HG00438.hp2 HG00544.hp1 HG02083.hp2 others(44): Show |
intron_variant | MODIFIER | c.522-995C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631355 | |||||||
| chr18:45631387 | G | A | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.522-963G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631387 | |||||||
| chr18:45631537 | G | C | 2 | a0006c0007t0003g0149 a0006c0007t0003g0150 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.522-813G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631537 | |||||||
| chr18:45631542 | T | C | 1 | a0002c0001t0011g0024 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.522-808T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631542 | |||||||
| chr18:45631725 | G | C | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.522-625G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631725 | |||||||
| chr18:45631738 | T | C | 1 | a0001c0004t0004g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.522-612T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45631738 | |||||||
| chr18:45632128 | GGTGTGTG others(11): Show |
G | 1 | a0002c0001t0001g0117 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.522-205_522-188del others(18): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45632128 | ||||||
| chr18:45632135 | GTGTGTGT others(3): Show |
G | 116 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0054 others(113): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.522-205_522-196del others(10): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45632135 | ||||||
| chr18:45632145 | TTG | T | 14 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0008g0249 others(11): Show |
14 | HG01109.hp2 HG01496.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.522-181_522-180del others(2): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45632145 | ||||||
| chr18:45632145 | TTGTG | T | 182 | a0001c0002t0003g0007 a0001c0002t0003g0031 a0001c0002t0003g0040 others(179): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.522-183_522-180del others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr18 | 45632145 | ||||||
| chr18:45632151 | G | T | 116 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0054 others(113): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.522-199G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45632151 | |||||||
| chr18:45632297 | G | A | 3 | a0001c0002t0003g0054 a0006c0007t0003g0056 a0011c0015t0003g0055 |
3 | NA18612.hp2 NA19000.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.522-53G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45632297 | |||||||
| chr18:45632323 | T | C | 9 | a0001c0002t0008g0249 a0001c0002t0008g0255 a0001c0002t0008g0311 others(6): Show |
9 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.522-27T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 4/19 | chr18 | 45632323 | |||||||
| chr18:45632540 | T | C | 1 | a0001c0004t0004g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.650+62T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45632540 | |||||||
| chr18:45632694 | T | G | 144 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0054 others(141): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.650+216T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45632694 | |||||||
| chr18:45632827 | G | A | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+349G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45632827 | |||||||
| chr18:45632923 | T | C | 1 | a0002c0001t0002g0380 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.650+445T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45632923 | |||||||
| chr18:45632973 | A | G | 317 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.650+495A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45632973 | |||||||
| chr18:45633040 | C | T | 27 | a0001c0002t0003g0332 a0003c0005t0001g0091 a0005c0008t0003g0181 others(24): Show |
27 | HG00609.hp1 HG00621.hp2 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.650+562C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633040 | |||||||
| chr18:45633164 | C | T | 2 | a0002c0001t0001g0226 a0002c0001t0002g0225 |
2 | HG01261.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.650+686C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633164 | |||||||
| chr18:45633315 | C | T | 1 | a0001c0002t0003g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.650+837C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633315 | |||||||
| chr18:45633507 | A | T | 1 | a0001c0002t0003g0250 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.650+1029A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633507 | |||||||
| chr18:45633508 | C | T | 144 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0054 others(141): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.650+1030C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633508 | |||||||
| chr18:45633525 | C | T | 1 | a0004c0003t0001g0029 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.650+1047C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633525 | |||||||
| chr18:45633608 | C | A | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1130C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633608 | |||||||
| chr18:45633651 | C | T | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1173C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633651 | |||||||
| chr18:45633735 | C | A | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.650+1257C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633735 | |||||||
| chr18:45633801 | A | G | 1 | a0001c0002t0003g0361 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.650+1323A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633801 | |||||||
| chr18:45633887 | T | C | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1409T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633887 | |||||||
| chr18:45633994 | T | C | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1516T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45633994 | |||||||
| chr18:45634068 | C | G | 1 | a0001c0002t0004g0376 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.650+1590C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634068 | |||||||
| chr18:45634097 | CA | C | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1626delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr18 | 45634097 | ||||||
| chr18:45634142 | C | G | 1 | a0012c0013t0003g0204 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.650+1664C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634142 | |||||||
| chr18:45634334 | G | A | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1856G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634334 | |||||||
| chr18:45634684 | G | A | 2 | a0003c0006t0002g0052 a0006c0007t0004g0170 |
2 | HG02683.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.650+2206G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634684 | |||||||
| chr18:45634684 | G | C | 1 | a0001c0002t0003g0099 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.650+2206G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634684 | |||||||
| chr18:45634709 | A | G | 9 | a0001c0002t0008g0249 a0001c0002t0008g0255 a0001c0002t0008g0311 others(6): Show |
9 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.650+2231A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634709 | |||||||
| chr18:45634781 | T | C | 1 | a0002c0001t0001g0025 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.651-2209T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634781 | |||||||
| chr18:45634782 | G | T | 3 | a0002c0001t0002g0128 a0002c0001t0002g0129 a0002c0001t0002g0130 |
3 | HG02055.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.651-2208G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45634782 | |||||||
| chr18:45634904 | CCA | C | 6 | a0001c0004t0004g0306 a0001c0004t0004g0307 a0001c0004t0004g0310 others(3): Show |
6 | HG02257.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.651-2083_651-2082d others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr18 | 45634904 | ||||||
| chr18:45635036 | A | G | 3 | a0006c0007t0003g0114 a0006c0007t0003g0164 a0009c0012t0005g0241 |
3 | HG00733.hp2 HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.651-1954A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635036 | |||||||
| chr18:45635074 | C | G | 1 | a0002c0001t0011g0024 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.651-1916C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635074 | |||||||
| chr18:45635117 | T | G | 1 | a0002c0001t0005g0100 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.651-1873T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635117 | |||||||
| chr18:45635145 | A | G | 146 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0054 others(143): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.651-1845A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635145 | |||||||
| chr18:45635451 | G | C | 5 | a0001c0004t0004g0306 a0001c0004t0004g0310 a0001c0004t0004g0348 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.651-1539G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635451 | |||||||
| chr18:45635578 | G | A | 1 | a0002c0001t0002g0034 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.651-1412G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635578 | |||||||
| chr18:45635674 | G | A | 2 | a0002c0001t0002g0358 a0002c0001t0002g0359 |
2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.651-1316G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635674 | |||||||
| chr18:45635692 | G | A | 2 | a0002c0001t0006g0125 a0002c0001t0006g0166 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.651-1298G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635692 | |||||||
| chr18:45635996 | C | G | 73 | a0001c0002t0003g0327 a0001c0002t0003g0355 a0001c0002t0003g0377 others(70): Show |
74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.651-994C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45635996 | |||||||
| chr18:45636045 | C | T | 275 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(272): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.651-945C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636045 | |||||||
| chr18:45636285 | C | G | 1 | a0008c0011t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.651-705C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636285 | |||||||
| chr18:45636294 | C | T | 1 | a0006c0007t0004g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.651-696C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636294 | |||||||
| chr18:45636311 | A | G | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.651-679A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636311 | |||||||
| chr18:45636411 | C | T | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.651-579C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636411 | |||||||
| chr18:45636450 | G | T | 2 | a0002c0001t0006g0125 a0002c0001t0006g0166 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.651-540G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636450 | |||||||
| chr18:45636479 | C | A | 2 | a0003c0006t0002g0121 a0003c0006t0002g0167 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.651-511C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636479 | |||||||
| chr18:45636754 | A | C | 1 | a0003c0005t0001g0081 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.651-236A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636754 | |||||||
| chr18:45636784 | C | CA | 12 | a0001c0002t0004g0376 a0001c0002t0008g0249 a0001c0002t0008g0255 others(9): Show |
12 | HG01496.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.651-196dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr18 | 45636784 | ||||||
| chr18:45636897 | G | A | 3 | a0002c0001t0001g0347 a0016c0021t0005g0346 a0016c0021t0005g0362 |
3 | HG03704.hp1 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.651-93G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 5/19 | chr18 | 45636897 | |||||||
| chr18:45637196 | C | A | 2 | a0003c0006t0002g0052 a0006c0007t0004g0170 |
2 | HG02683.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.843+14C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637196 | |||||||
| chr18:45637227 | G | T | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+45G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637227 | |||||||
| chr18:45637298 | G | C | 23 | a0001c0002t0003g0293 a0001c0002t0003g0294 a0001c0002t0003g0304 others(20): Show |
23 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.843+116G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637298 | |||||||
| chr18:45637525 | A | G | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+343A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637525 | |||||||
| chr18:45637647 | G | A | 1 | a0006c0007t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.843+465G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637647 | |||||||
| chr18:45637738 | G | T | 1 | a0004c0003t0001g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.843+556G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637738 | |||||||
| chr18:45637900 | C | A | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.843+718C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45637900 | |||||||
| chr18:45638005 | T | C | 1 | a0016c0021t0005g0362 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.843+823T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638005 | |||||||
| chr18:45638080 | T | C | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+898T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638080 | |||||||
| chr18:45638083 | G | A | 1 | a0004c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.843+901G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638083 | |||||||
| chr18:45638088 | C | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.843+906C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638088 | |||||||
| chr18:45638099 | G | A | 1 | a0001c0002t0003g0007 | 2 | NA18959.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.843+917G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638099 | |||||||
| chr18:45638107 | G | C | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.843+925G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638107 | |||||||
| chr18:45638207 | G | A | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+1025G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638207 | |||||||
| chr18:45638391 | C | T | 7 | a0001c0002t0008g0249 a0001c0002t0008g0255 a0001c0002t0008g0311 others(4): Show |
7 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+1209C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638391 | |||||||
| chr18:45638464 | C | G | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.843+1282C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638464 | |||||||
| chr18:45638692 | A | G | 1 | a0002c0001t0002g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.844-1054A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638692 | |||||||
| chr18:45638692 | A | T | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.844-1054A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638692 | |||||||
| chr18:45638952 | A | G | 1 | a0013c0016t0001g0230 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.844-794A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638952 | |||||||
| chr18:45638960 | G | A | 1 | a0005c0010t0003g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.844-786G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45638960 | |||||||
| chr18:45639013 | C | A | 275 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(272): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.844-733C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639013 | |||||||
| chr18:45639179 | G | A | 1 | a0006c0007t0003g0164 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.844-567G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639179 | |||||||
| chr18:45639287 | C | A | 10 | a0001c0002t0003g0092 a0002c0001t0001g0095 a0002c0001t0002g0032 others(7): Show |
12 | HG00673.hp1 HG02015.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.844-459C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639287 | |||||||
| chr18:45639311 | G | C | 1 | a0004c0003t0020g0026 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.844-435G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639311 | |||||||
| chr18:45639356 | T | C | 1 | a0005c0010t0013g0205 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.844-390T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639356 | |||||||
| chr18:45639373 | G | A | 5 | a0001c0004t0004g0251 a0005c0010t0004g0175 a0005c0010t0004g0176 others(2): Show |
5 | HG02572.hp1 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-373G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639373 | |||||||
| chr18:45639414 | G | A | 4 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0016g0259 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-332G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639414 | |||||||
| chr18:45639456 | A | C | 1 | a0004c0003t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.844-290A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639456 | |||||||
| chr18:45639723 | C | T | 1 | a0004c0003t0001g0341 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.844-23C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 6/19 | chr18 | 45639723 | |||||||
| chr18:45640019 | C | T | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.991+126C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640019 | |||||||
| chr18:45640074 | A | T | 3 | a0001c0004t0004g0340 a0001c0022t0004g0338 a0001c0022t0004g0339 |
3 | HG01192.hp1 HG02145.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.991+181A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640074 | |||||||
| chr18:45640154 | T | C | 2 | a0002c0001t0006g0125 a0002c0001t0006g0166 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.991+261T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640154 | |||||||
| chr18:45640191 | A | G | 376 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(373): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.991+298A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640191 | |||||||
| chr18:45640245 | C | A | 1 | a0004c0003t0001g0314 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.991+352C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640245 | |||||||
| chr18:45640275 | TA | T | 10 | a0001c0002t0003g0293 a0001c0002t0003g0294 a0001c0002t0003g0304 others(7): Show |
10 | HG01256.hp1 HG02895.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.991+396delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr18 | 45640275 | ||||||
| chr18:45640366 | A | G | 87 | a0001c0002t0003g0007 a0001c0002t0003g0031 a0001c0002t0003g0076 others(84): Show |
90 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.991+473A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640366 | |||||||
| chr18:45640422 | G | A | 1 | a0004c0003t0001g0075 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.991+529G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640422 | |||||||
| chr18:45640522 | T | C | 316 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(313): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.991+629T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640522 | |||||||
| chr18:45640813 | G | A | 150 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0040 others(147): Show |
164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.992-396G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640813 | |||||||
| chr18:45640863 | T | C | 15 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(12): Show |
18 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.992-346T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640863 | |||||||
| chr18:45640881 | T | G | 322 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.992-328T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640881 | |||||||
| chr18:45640910 | G | T | 322 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.992-299G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45640910 | |||||||
| chr18:45641056 | G | A | 1 | a0004c0003t0001g0291 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.992-153G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45641056 | |||||||
| chr18:45641124 | C | T | 2 | a0007c0009t0001g0105 a0007c0009t0001g0109 |
2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.992-85C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45641124 | |||||||
| chr18:45641194 | C | T | 2 | a0002c0001t0006g0125 a0002c0001t0006g0166 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.992-15C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 7/19 | chr18 | 45641194 | |||||||
| chr18:45641371 | G | A | 1 | a0001c0002t0008g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1126+28G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45641371 | |||||||
| chr18:45641376 | T | C | 322 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1126+33T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45641376 | |||||||
| chr18:45641581 | G | A | 3 | a0004c0003t0001g0323 a0004c0003t0001g0324 a0004c0003t0021g0349 |
3 | HG02698.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1126+238G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45641581 | |||||||
| chr18:45641823 | C | T | 3 | a0001c0004t0016g0259 a0002c0001t0006g0125 a0002c0001t0006g0166 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1126+480C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45641823 | |||||||
| chr18:45641941 | C | A | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1126+598C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45641941 | |||||||
| chr18:45642115 | C | G | 6 | a0001c0002t0004g0142 a0003c0005t0002g0139 a0003c0018t0002g0135 others(3): Show |
6 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126+772C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642115 | |||||||
| chr18:45642133 | A | G | 1 | a0003c0006t0002g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1126+790A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642133 | |||||||
| chr18:45642193 | G | C | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1126+850G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642193 | |||||||
| chr18:45642200 | G | A | 4 | a0001c0004t0003g0051 a0002c0001t0005g0153 a0005c0010t0003g0196 others(1): Show |
4 | HG00642.hp2 HG01261.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126+857G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642200 | |||||||
| chr18:45642339 | A | C | 1 | a0002c0001t0002g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1127-793A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642339 | |||||||
| chr18:45642367 | C | T | 109 | a0001c0002t0003g0040 a0001c0002t0003g0054 a0001c0002t0003g0071 others(106): Show |
120 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(117): Show |
intron_variant | MODIFIER | c.1127-765C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642367 | |||||||
| chr18:45642376 | T | C | 321 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(318): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1127-756T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642376 | |||||||
| chr18:45642458 | C | T | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1127-674C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642458 | |||||||
| chr18:45642492 | G | A | 2 | a0005c0008t0003g0207 a0005c0008t0003g0208 |
2 | NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1127-640G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642492 | |||||||
| chr18:45642507 | G | A | 18 | a0001c0002t0003g0296 a0001c0002t0003g0361 a0001c0002t0004g0360 others(15): Show |
20 | HG00140.hp2 HG00438.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1127-625G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642507 | |||||||
| chr18:45642538 | G | A | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1127-594G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642538 | |||||||
| chr18:45642544 | G | A | 156 | a0001c0002t0003g0031 a0001c0002t0003g0073 a0001c0002t0003g0074 others(153): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1127-588G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642544 | |||||||
| chr18:45642575 | C | T | 8 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1127-557C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642575 | |||||||
| chr18:45642601 | C | G | 1 | a0005c0010t0004g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1127-531C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642601 | |||||||
| chr18:45642611 | T | C | 1 | a0005c0008t0003g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1127-521T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 8/19 | chr18 | 45642611 | |||||||
| chr18:45643604 | C | T | 1 | a0003c0005t0002g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1177-382C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 9/19 | chr18 | 45643604 | |||||||
| chr18:45643693 | C | T | 8 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-293C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 9/19 | chr18 | 45643693 | |||||||
| chr18:45643723 | A | G | 1 | a0001c0004t0016g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1177-263A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 9/19 | chr18 | 45643723 | |||||||
| chr18:45643795 | G | T | 6 | a0001c0004t0004g0251 a0005c0010t0004g0175 a0005c0010t0004g0176 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-191G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 9/19 | chr18 | 45643795 | |||||||
| chr18:45644188 | G | A | 6 | a0001c0004t0004g0251 a0005c0010t0004g0175 a0005c0010t0004g0176 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1351+28G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644188 | |||||||
| chr18:45644368 | T | G | 154 | a0001c0002t0003g0031 a0001c0002t0003g0073 a0001c0002t0003g0074 others(151): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1351+208T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644368 | |||||||
| chr18:45644399 | C | T | 1 | a0004c0003t0001g0162 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1351+239C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644399 | |||||||
| chr18:45644400 | G | A | 2 | a0005c0008t0003g0209 a0005c0010t0004g0237 |
2 | NA18954.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1351+240G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644400 | |||||||
| chr18:45644445 | C | T | 1 | a0004c0003t0001g0341 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1351+285C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644445 | |||||||
| chr18:45644460 | T | G | 24 | a0001c0002t0003g0332 a0003c0005t0001g0091 a0004c0003t0001g0232 others(21): Show |
24 | HG00609.hp1 HG00621.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.1351+300T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644460 | |||||||
| chr18:45644542 | T | G | 1 | a0016c0021t0005g0362 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1351+382T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644542 | |||||||
| chr18:45644682 | G | A | 1 | a0003c0033t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1351+522G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644682 | |||||||
| chr18:45644935 | G | A | 156 | a0001c0002t0003g0031 a0001c0002t0003g0073 a0001c0002t0003g0074 others(153): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1351+775G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644935 | |||||||
| chr18:45644946 | C | G | 143 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(140): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1351+786C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45644946 | |||||||
| chr18:45645088 | C | T | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1351+928C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645088 | |||||||
| chr18:45645278 | G | A | 1 | a0001c0004t0016g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1351+1118G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645278 | |||||||
| chr18:45645582 | A | G | 9 | a0001c0002t0004g0376 a0001c0004t0004g0251 a0003c0033t0002g0134 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1351+1422A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645582 | |||||||
| chr18:45645619 | A | ATATATAC others(35): Show |
7 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(4): Show |
9 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(46): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(61): Show |
24 | a0001c0002t0003g0007 a0001c0002t0003g0079 a0001c0002t0003g0108 others(21): Show |
25 | HG01167.hp1 HG01169.hp2 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(72): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(59): Show |
1 | a0001c0004t0004g0260 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(70): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(39): Show |
3 | a0002c0001t0002g0225 a0004c0003t0001g0088 a0006c0007t0004g0223 |
3 | HG01255.hp1 HG01261.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(50): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(37): Show |
7 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0002c0001t0002g0268 others(4): Show |
8 | HG01109.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(48): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(77): Show |
1 | a0002c0001t0002g0356 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(88): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(81): Show |
1 | a0009c0012t0002g0206 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(92): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(61): Show |
8 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(72): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(41): Show |
65 | a0001c0002t0003g0040 a0001c0002t0003g0054 a0001c0002t0003g0071 others(62): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(52): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(39): Show |
8 | a0001c0004t0016g0259 a0002c0001t0002g0027 a0002c0001t0002g0035 others(5): Show |
8 | HG01975.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(50): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(37): Show |
1 | a0002c0001t0002g0104 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(48): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(65): Show |
2 | a0002c0001t0006g0125 a0002c0001t0006g0166 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(76): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(67): Show |
2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(78): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(43): Show |
13 | a0001c0023t0003g0374 a0002c0001t0002g0036 a0002c0001t0019g0041 others(10): Show |
13 | HG01358.hp1 HG02148.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(54): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(41): Show |
6 | a0002c0001t0001g0095 a0002c0001t0002g0015 a0002c0001t0002g0023 others(3): Show |
6 | HG01070.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(52): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(39): Show |
3 | a0002c0001t0002g0128 a0002c0001t0002g0129 a0002c0001t0002g0130 |
3 | HG02055.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(50): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(45): Show |
5 | a0001c0002t0003g0092 a0002c0001t0002g0358 a0002c0001t0002g0359 others(2): Show |
7 | HG00673.hp1 HG02015.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(56): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(43): Show |
1 | a0003c0005t0017g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(54): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(19): Show |
1 | a0001c0004t0004g0065 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(30): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645619 | A | ATATATAC others(17): Show |
2 | a0003c0005t0007g0048 a0003c0005t0007g0049 |
2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(28): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645619 | ||||||
| chr18:45645622 | T | TATACATA others(29): Show |
2 | a0001c0022t0004g0338 a0001c0022t0004g0339 |
2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(40): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(23): Show |
57 | a0001c0002t0003g0031 a0001c0002t0003g0076 a0001c0002t0003g0110 others(54): Show |
59 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(34): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(25): Show |
7 | a0001c0002t0003g0078 a0002c0001t0002g0290 a0003c0006t0002g0067 others(4): Show |
7 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(36): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(27): Show |
29 | a0001c0002t0003g0099 a0001c0002t0003g0106 a0001c0002t0003g0283 others(26): Show |
30 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(38): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(61): Show |
1 | a0003c0006t0002g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(72): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(29): Show |
36 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0115 others(33): Show |
36 | HG00423.hp1 HG00733.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(40): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(31): Show |
13 | a0002c0001t0005g0334 a0002c0001t0005g0337 a0003c0006t0002g0121 others(10): Show |
13 | HG01074.hp2 HG01081.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(42): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(33): Show |
5 | a0001c0004t0004g0340 a0003c0006t0002g0146 a0003c0006t0002g0147 others(2): Show |
5 | HG01081.hp2 HG01891.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351+1463_1351+146 others(44): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATACATA others(45): Show |
1 | a0006c0007t0003g0343 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(56): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645622 | T | TATATATA others(19): Show |
1 | a0004c0003t0001g0324 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1351+1463_1351+146 others(30): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45645622 | ||||||
| chr18:45645648 | G | A | 161 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(158): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1351+1488G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645648 | |||||||
| chr18:45645767 | A | T | 1 | a0004c0003t0001g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1351+1607A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645767 | |||||||
| chr18:45645954 | G | A | 8 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1351+1794G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645954 | |||||||
| chr18:45645978 | A | G | 152 | a0001c0002t0003g0031 a0001c0002t0003g0073 a0001c0002t0003g0074 others(149): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1351+1818A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645978 | |||||||
| chr18:45645988 | T | G | 12 | a0002c0001t0002g0023 a0002c0001t0002g0044 a0002c0001t0002g0046 others(9): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1351+1828T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45645988 | |||||||
| chr18:45646051 | T | C | 1 | a0002c0001t0002g0068 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1351+1891T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646051 | |||||||
| chr18:45646135 | G | A | 1 | a0017c0036t0002g0288 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1351+1975G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646135 | |||||||
| chr18:45646360 | A | G | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351+2200A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646360 | |||||||
| chr18:45646379 | C | T | 2 | a0001c0004t0004g0277 a0001c0004t0004g0278 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1351+2219C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646379 | |||||||
| chr18:45646475 | C | A | 151 | a0001c0002t0003g0031 a0001c0002t0003g0073 a0001c0002t0003g0074 others(148): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1351+2315C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646475 | |||||||
| chr18:45646725 | T | C | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351+2565T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646725 | |||||||
| chr18:45646786 | G | A | 148 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(145): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1351+2626G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646786 | |||||||
| chr18:45646894 | C | T | 1 | a0002c0001t0001g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1351+2734C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45646894 | |||||||
| chr18:45647008 | G | T | 1 | a0012c0013t0022g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1351+2848G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647008 | |||||||
| chr18:45647240 | A | G | 152 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(149): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1351+3080A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647240 | |||||||
| chr18:45647324 | A | G | 323 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(320): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1351+3164A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647324 | |||||||
| chr18:45647428 | G | A | 322 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1351+3268G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647428 | |||||||
| chr18:45647438 | T | C | 151 | a0001c0002t0003g0031 a0001c0002t0003g0073 a0001c0002t0003g0074 others(148): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1351+3278T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647438 | |||||||
| chr18:45647781 | C | CTT | 170 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(167): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1351+3622_1351+362 others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45647781 | ||||||
| chr18:45647891 | C | T | 1 | a0003c0033t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1351+3731C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647891 | |||||||
| chr18:45647949 | T | C | 170 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(167): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1351+3789T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45647949 | |||||||
| chr18:45648052 | T | A | 163 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1351+3892T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648052 | |||||||
| chr18:45648061 | A | AGTTT | 163 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1351+3901_1351+390 others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648061 | |||||||
| chr18:45648101 | TACC | T | 3 | a0001c0004t0016g0259 a0002c0001t0006g0125 a0002c0001t0006g0166 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1351+3944_1351+394 others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648101 | ||||||
| chr18:45648195 | C | CT | 17 | a0001c0002t0003g0106 a0001c0004t0003g0051 a0003c0005t0002g0038 others(14): Show |
18 | HG00544.hp2 HG00621.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1351+4063dupT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | C | CTTT | 7 | a0001c0004t0004g0251 a0002c0001t0002g0193 a0005c0010t0004g0175 others(4): Show |
8 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1351+4061_1351+406 others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | C | CTTTTTTT others(5): Show |
6 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1351+4052_1351+406 others(16): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | C | CTTTTTTT others(6): Show |
3 | a0001c0002t0008g0311 a0001c0002t0008g0312 a0001c0023t0003g0374 |
3 | HG02258.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1351+4051_1351+406 others(17): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | C | CTTTTTTT others(7): Show |
1 | a0015c0017t0002g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1351+4050_1351+406 others(18): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | C | CTTTTTTT others(8): Show |
1 | a0015c0017t0002g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1351+4049_1351+406 others(19): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | CT | C | 103 | a0001c0002t0003g0073 a0001c0002t0003g0076 a0001c0002t0003g0110 others(100): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1351+4063delT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | CTTTTTTT others(6): Show |
C | 4 | a0001c0002t0003g0168 a0002c0001t0001g0025 a0006c0007t0003g0057 others(1): Show |
4 | HG02735.hp2 NA18985.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+4051_1351+406 others(17): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648195 | CTTTTTTT others(7): Show |
C | 145 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(142): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1351+4050_1351+406 others(18): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45648195 | ||||||
| chr18:45648266 | C | T | 1 | a0001c0004t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1351+4106C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648266 | |||||||
| chr18:45648267 | A | G | 1 | a0001c0004t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1351+4107A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648267 | |||||||
| chr18:45648269 | C | G | 1 | a0001c0004t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1351+4109C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648269 | |||||||
| chr18:45648274 | G | C | 1 | a0001c0004t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1351+4114G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648274 | |||||||
| chr18:45648300 | G | T | 161 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(158): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1351+4140G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648300 | |||||||
| chr18:45648427 | G | A | 5 | a0001c0002t0003g0005 a0001c0002t0003g0017 a0001c0002t0003g0248 others(2): Show |
7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1351+4267G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648427 | |||||||
| chr18:45648481 | A | C | 1 | a0001c0004t0004g0366 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1351+4321A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648481 | |||||||
| chr18:45648482 | G | C | 1 | a0001c0004t0004g0366 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1351+4322G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648482 | |||||||
| chr18:45648492 | A | G | 162 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(159): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1351+4332A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648492 | |||||||
| chr18:45648494 | C | T | 158 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(155): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1351+4334C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648494 | |||||||
| chr18:45648495 | A | G | 162 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(159): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1351+4335A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648495 | |||||||
| chr18:45648497 | G | A | 91 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(88): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1351+4337G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648497 | |||||||
| chr18:45648539 | C | A | 7 | a0001c0004t0004g0148 a0001c0004t0004g0306 a0001c0004t0004g0307 others(4): Show |
7 | HG02257.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351+4379C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648539 | |||||||
| chr18:45648602 | C | T | 162 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(159): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1351+4442C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648602 | |||||||
| chr18:45648741 | CTAAT | C | 109 | a0001c0002t0003g0040 a0001c0002t0003g0054 a0001c0002t0003g0071 others(106): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1351+4582_1351+458 others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648741 | |||||||
| chr18:45648815 | G | A | 1 | a0001c0002t0003g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1351+4655G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648815 | |||||||
| chr18:45648821 | G | C | 163 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1351+4661G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648821 | |||||||
| chr18:45648853 | T | G | 1 | a0021c0029t0004g0321 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1351+4693T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648853 | |||||||
| chr18:45648922 | C | T | 6 | a0001c0004t0004g0148 a0001c0004t0004g0306 a0001c0004t0004g0310 others(3): Show |
6 | HG02257.hp1 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1351+4762C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648922 | |||||||
| chr18:45648944 | C | T | 322 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1351+4784C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648944 | |||||||
| chr18:45648974 | A | G | 1 | a0003c0033t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1351+4814A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648974 | |||||||
| chr18:45648995 | C | A | 1 | a0004c0003t0001g0075 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1351+4835C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648995 | |||||||
| chr18:45648998 | T | C | 164 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(161): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1351+4838T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45648998 | |||||||
| chr18:45649022 | A | C | 3 | a0001c0004t0016g0259 a0002c0001t0006g0125 a0002c0001t0006g0166 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1351+4862A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649022 | |||||||
| chr18:45649180 | A | AAAAAAC | 163 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1351+5032_1351+503 others(10): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45649180 | ||||||
| chr18:45649180 | A | AAAAAACA others(5): Show |
1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1351+5026_1351+503 others(16): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45649180 | ||||||
| chr18:45649207 | G | A | 1 | a0008c0011t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1351+5047G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649207 | |||||||
| chr18:45649289 | G | A | 95 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(92): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1351+5129G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649289 | |||||||
| chr18:45649324 | T | C | 163 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1351+5164T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649324 | |||||||
| chr18:45649390 | G | A | 163 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1351+5230G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649390 | |||||||
| chr18:45649466 | C | T | 95 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(92): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1351+5306C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649466 | |||||||
| chr18:45649486 | C | A | 89 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(86): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1351+5326C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649486 | |||||||
| chr18:45649498 | C | G | 2 | a0001c0004t0004g0320 a0002c0001t0002g0319 |
2 | NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1351+5338C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649498 | |||||||
| chr18:45649731 | T | G | 105 | a0001c0002t0003g0040 a0001c0002t0003g0054 a0001c0002t0003g0071 others(102): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1351+5571T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649731 | |||||||
| chr18:45649869 | C | A | 1 | a0019c0031t0003g0252 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1351+5709C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649869 | |||||||
| chr18:45649893 | G | A | 1 | a0006c0007t0003g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1351+5733G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649893 | |||||||
| chr18:45649899 | C | T | 2 | a0005c0008t0004g0171 a0008c0011t0001g0172 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1351+5739C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649899 | |||||||
| chr18:45649900 | G | A | 2 | a0006c0007t0003g0243 a0007c0009t0001g0022 |
2 | HG02040.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1351+5740G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45649900 | |||||||
| chr18:45650009 | G | A | 2 | a0005c0008t0004g0171 a0008c0011t0001g0172 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1351+5849G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650009 | |||||||
| chr18:45650093 | G | A | 3 | a0002c0001t0002g0378 a0020c0026t0004g0363 a0022c0027t0009g0187 |
3 | HG02970.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1351+5933G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650093 | |||||||
| chr18:45650102 | A | T | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351+5942A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650102 | |||||||
| chr18:45650107 | A | C | 164 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(161): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1351+5947A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650107 | |||||||
| chr18:45650171 | TCCATTTG others(1): Show |
T | 321 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(318): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1351+6015_1351+602 others(12): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45650171 | ||||||
| chr18:45650519 | A | G | 1 | a0003c0033t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1351+6359A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650519 | |||||||
| chr18:45650746 | GT | G | 161 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(158): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1351+6590delT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45650746 | ||||||
| chr18:45650801 | A | G | 322 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1351+6641A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650801 | |||||||
| chr18:45650928 | G | A | 96 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(93): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1351+6768G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45650928 | |||||||
| chr18:45651183 | C | T | 96 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(93): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1351+7023C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651183 | |||||||
| chr18:45651270 | G | T | 59 | a0001c0002t0003g0031 a0001c0002t0003g0076 a0001c0002t0003g0078 others(56): Show |
61 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1351+7110G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651270 | |||||||
| chr18:45651353 | A | G | 96 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0099 others(93): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1351+7193A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651353 | |||||||
| chr18:45651620 | C | T | 1 | a0001c0004t0016g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1351+7460C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651620 | |||||||
| chr18:45651657 | G | A | 325 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0017 others(322): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1351+7497G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651657 | |||||||
| chr18:45651670 | G | A | 9 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0002c0001t0002g0268 others(6): Show |
10 | HG01109.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1351+7510G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651670 | |||||||
| chr18:45651724 | T | C | 1 | a0002c0001t0002g0378 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1351+7564T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651724 | |||||||
| chr18:45651749 | C | T | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351+7589C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651749 | |||||||
| chr18:45651808 | C | T | 3 | a0001c0004t0004g0126 a0003c0005t0002g0090 a0003c0005t0002g0140 |
3 | HG02717.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1351+7648C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651808 | |||||||
| chr18:45651888 | C | A | 1 | a0009c0012t0005g0222 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1351+7728C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651888 | |||||||
| chr18:45651909 | A | G | 1 | a0002c0001t0002g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1351+7749A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651909 | |||||||
| chr18:45651961 | A | G | 1 | a0001c0004t0003g0051 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1351+7801A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45651961 | |||||||
| chr18:45652016 | G | A | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351+7856G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652016 | |||||||
| chr18:45652195 | C | T | 1 | a0006c0007t0004g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1351+8035C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652195 | |||||||
| chr18:45652309 | A | C | 174 | a0001c0002t0003g0007 a0001c0002t0003g0040 a0001c0002t0003g0054 others(171): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1351+8149A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652309 | |||||||
| chr18:45652576 | G | A | 2 | a0003c0005t0007g0267 a0003c0005t0007g0295 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1351+8416G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652576 | |||||||
| chr18:45652597 | C | T | 1 | a0001c0002t0008g0249 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1351+8437C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652597 | |||||||
| chr18:45652616 | C | T | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1351+8456C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652616 | |||||||
| chr18:45652623 | T | C | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1351+8463T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652623 | |||||||
| chr18:45652667 | C | T | 283 | a0001c0002t0003g0071 a0001c0002t0003g0092 a0001c0002t0003g0133 others(280): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1351+8507C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652667 | |||||||
| chr18:45652696 | G | C | 3 | a0001c0004t0004g0261 a0003c0006t0002g0229 a0014c0020t0004g0275 |
3 | HG00099.hp2 HG01243.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1351+8536G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652696 | |||||||
| chr18:45652961 | G | T | 10 | a0001c0002t0008g0249 a0001c0004t0004g0126 a0001c0004t0004g0127 others(7): Show |
10 | HG02257.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1351+8801G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45652961 | |||||||
| chr18:45653113 | G | C | 12 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(9): Show |
13 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1351+8953G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653113 | |||||||
| chr18:45653226 | C | G | 11 | a0001c0002t0008g0249 a0001c0004t0004g0126 a0001c0004t0004g0127 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1351+9066C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653226 | |||||||
| chr18:45653435 | T | C | 22 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0008g0249 others(19): Show |
23 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(20): Show |
intron_variant | MODIFIER | c.1351+9275T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653435 | |||||||
| chr18:45653664 | G | T | 2 | a0003c0006t0002g0165 a0003c0006t0002g0305 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1351+9504G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653664 | |||||||
| chr18:45653687 | G | A | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1351+9527G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653687 | |||||||
| chr18:45653820 | G | A | 1 | a0001c0002t0003g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1351+9660G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653820 | |||||||
| chr18:45653845 | C | T | 1 | a0003c0005t0017g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1351+9685C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653845 | |||||||
| chr18:45653921 | C | T | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1351+9761C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45653921 | |||||||
| chr18:45654001 | C | T | 1 | a0001c0002t0008g0249 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1352-9784C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654001 | |||||||
| chr18:45654022 | C | A | 2 | a0008c0025t0009g0203 a0022c0027t0009g0187 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1352-9763C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654022 | |||||||
| chr18:45654137 | T | TGG | 195 | a0001c0002t0008g0249 a0001c0004t0003g0051 a0001c0004t0004g0020 others(192): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1352-9642_1352-964 others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45654137 | ||||||
| chr18:45654145 | A | G | 227 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(224): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1352-9640A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654145 | |||||||
| chr18:45654226 | G | A | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1352-9559G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654226 | |||||||
| chr18:45654399 | C | T | 4 | a0001c0002t0003g0040 a0005c0008t0003g0231 a0011c0015t0003g0055 others(1): Show |
4 | HG00621.hp2 NA18612.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352-9386C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654399 | |||||||
| chr18:45654424 | G | A | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1352-9361G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654424 | |||||||
| chr18:45654490 | C | CG | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1352-9295_1352-929 others(5): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654490 | |||||||
| chr18:45654501 | A | G | 208 | a0001c0002t0008g0249 a0001c0004t0003g0051 a0001c0004t0004g0020 others(205): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1352-9284A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654501 | |||||||
| chr18:45654835 | G | A | 205 | a0001c0002t0008g0249 a0001c0004t0003g0051 a0001c0004t0004g0020 others(202): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1352-8950G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654835 | |||||||
| chr18:45654939 | G | A | 205 | a0001c0002t0008g0249 a0001c0004t0003g0051 a0001c0004t0004g0020 others(202): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1352-8846G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45654939 | |||||||
| chr18:45655045 | C | G | 1 | a0001c0002t0003g0296 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1352-8740C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655045 | |||||||
| chr18:45655288 | G | T | 1 | a0002c0001t0002g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1352-8497G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655288 | |||||||
| chr18:45655337 | G | T | 1 | a0001c0002t0004g0376 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1352-8448G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655337 | |||||||
| chr18:45655373 | T | G | 1 | a0001c0004t0004g0351 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1352-8412T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655373 | |||||||
| chr18:45655381 | C | T | 1 | a0001c0004t0004g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1352-8404C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655381 | |||||||
| chr18:45655464 | T | C | 1 | a0001c0002t0004g0376 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1352-8321T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655464 | |||||||
| chr18:45655534 | T | C | 129 | a0001c0004t0004g0127 a0002c0001t0001g0025 a0002c0001t0001g0037 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1352-8251T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655534 | |||||||
| chr18:45655571 | G | A | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-8214G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655571 | |||||||
| chr18:45655651 | C | T | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1352-8134C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655651 | |||||||
| chr18:45655850 | C | A | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1352-7935C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655850 | |||||||
| chr18:45655917 | T | G | 218 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(215): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1352-7868T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45655917 | |||||||
| chr18:45656047 | G | A | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1352-7738G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656047 | |||||||
| chr18:45656099 | C | G | 1 | a0001c0002t0008g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1352-7686C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656099 | |||||||
| chr18:45656111 | A | G | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1352-7674A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656111 | |||||||
| chr18:45656140 | C | T | 206 | a0001c0002t0004g0142 a0001c0002t0004g0360 a0001c0004t0003g0051 others(203): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1352-7645C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656140 | |||||||
| chr18:45656173 | A | C | 218 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(215): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1352-7612A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656173 | |||||||
| chr18:45656220 | G | A | 1 | a0001c0002t0004g0360 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1352-7565G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656220 | |||||||
| chr18:45656330 | G | GA | 204 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1352-7454dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45656330 | ||||||
| chr18:45656361 | G | A | 5 | a0001c0004t0004g0251 a0003c0018t0002g0030 a0005c0010t0004g0175 others(2): Show |
5 | HG01516.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1352-7424G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656361 | |||||||
| chr18:45656381 | A | G | 204 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1352-7404A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656381 | |||||||
| chr18:45656465 | G | A | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-7320G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656465 | |||||||
| chr18:45656558 | T | C | 3 | a0004c0003t0001g0075 a0004c0003t0001g0082 a0004c0003t0001g0088 |
3 | HG00544.hp1 NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1352-7227T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656558 | |||||||
| chr18:45656561 | T | C | 1 | a0005c0008t0003g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1352-7224T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656561 | |||||||
| chr18:45656629 | G | A | 76 | a0002c0001t0001g0025 a0002c0001t0001g0095 a0002c0001t0001g0096 others(73): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1352-7156G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656629 | |||||||
| chr18:45656653 | G | A | 1 | a0002c0001t0002g0378 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1352-7132G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656653 | |||||||
| chr18:45656681 | T | C | 16 | a0001c0004t0004g0126 a0001c0004t0004g0127 a0001c0004t0004g0148 others(13): Show |
16 | HG00673.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1352-7104T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656681 | |||||||
| chr18:45656716 | A | C | 204 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1352-7069A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656716 | |||||||
| chr18:45656766 | C | T | 126 | a0002c0001t0001g0025 a0002c0001t0001g0037 a0002c0001t0001g0083 others(123): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1352-7019C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656766 | |||||||
| chr18:45656796 | C | A | 1 | a0001c0002t0003g0099 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1352-6989C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656796 | |||||||
| chr18:45656796 | C | T | 7 | a0004c0003t0001g0029 a0004c0003t0001g0323 a0004c0003t0001g0324 others(4): Show |
7 | HG01099.hp2 HG01106.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352-6989C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656796 | |||||||
| chr18:45656893 | C | G | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-6892C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656893 | |||||||
| chr18:45656952 | T | C | 1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1352-6833T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656952 | |||||||
| chr18:45656965 | A | G | 18 | a0001c0004t0003g0051 a0001c0004t0004g0065 a0001c0004t0004g0320 others(15): Show |
18 | HG00642.hp2 HG01074.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1352-6820A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45656965 | |||||||
| chr18:45657081 | G | A | 1 | a0004c0003t0001g0315 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1352-6704G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657081 | |||||||
| chr18:45657119 | A | G | 1 | a0001c0004t0016g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1352-6666A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657119 | |||||||
| chr18:45657129 | G | A | 2 | a0003c0006t0002g0165 a0003c0006t0002g0305 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1352-6656G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657129 | |||||||
| chr18:45657222 | A | G | 2 | a0003c0006t0002g0165 a0003c0006t0002g0305 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1352-6563A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657222 | |||||||
| chr18:45657325 | C | CAA | 14 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(11): Show |
15 | HG00673.hp2 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1352-6449_1352-644 others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45657325 | ||||||
| chr18:45657418 | C | T | 1 | a0004c0003t0001g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1352-6367C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657418 | |||||||
| chr18:45657468 | C | G | 204 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1352-6317C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657468 | |||||||
| chr18:45657488 | G | GA | 6 | a0001c0004t0004g0186 a0001c0004t0016g0259 a0004c0003t0001g0308 others(3): Show |
7 | HG01884.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-6282dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45657488 | ||||||
| chr18:45657488 | GA | G | 6 | a0001c0004t0013g0322 a0002c0001t0002g0193 a0008c0025t0009g0203 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-6282delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45657488 | ||||||
| chr18:45657519 | AAAGG | A | 126 | a0002c0001t0001g0025 a0002c0001t0001g0037 a0002c0001t0001g0083 others(123): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1352-6247_1352-624 others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45657519 | ||||||
| chr18:45657527 | G | C | 1 | a0012c0013t0022g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1352-6258G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657527 | |||||||
| chr18:45657671 | T | A | 1 | a0005c0010t0013g0205 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1352-6114T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657671 | |||||||
| chr18:45657784 | T | C | 6 | a0003c0006t0002g0165 a0003c0006t0002g0305 a0003c0006t0006g0185 others(3): Show |
6 | HG00673.hp2 HG02257.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-6001T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657784 | |||||||
| chr18:45657829 | G | C | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1352-5956G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45657829 | |||||||
| chr18:45658057 | C | T | 215 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(212): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1352-5728C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658057 | |||||||
| chr18:45658170 | T | C | 1 | a0003c0005t0001g0072 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1352-5615T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658170 | |||||||
| chr18:45658353 | T | G | 215 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(212): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1352-5432T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658353 | |||||||
| chr18:45658460 | A | G | 60 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1352-5325A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658460 | |||||||
| chr18:45658461 | G | A | 1 | a0001c0002t0003g0269 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1352-5324G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658461 | |||||||
| chr18:45658528 | C | T | 60 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1352-5257C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658528 | |||||||
| chr18:45658568 | G | A | 1 | a0007c0009t0001g0053 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1352-5217G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658568 | |||||||
| chr18:45658580 | CA | C | 60 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1352-5193delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45658580 | ||||||
| chr18:45658647 | G | A | 1 | a0006c0007t0003g0002 | 3 | HG00280.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1352-5138G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658647 | |||||||
| chr18:45658832 | G | A | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-4953G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658832 | |||||||
| chr18:45658833 | C | A | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-4952C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658833 | |||||||
| chr18:45658885 | T | C | 1 | a0002c0001t0001g0285 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1352-4900T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658885 | |||||||
| chr18:45658938 | T | C | 60 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1352-4847T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45658938 | |||||||
| chr18:45659240 | A | G | 1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1352-4545A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659240 | |||||||
| chr18:45659385 | A | T | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1352-4400A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659385 | |||||||
| chr18:45659429 | C | T | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-4356C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659429 | |||||||
| chr18:45659430 | G | A | 56 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(53): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1352-4355G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659430 | |||||||
| chr18:45659440 | T | C | 6 | a0001c0002t0003g0054 a0001c0002t0003g0073 a0001c0002t0003g0074 others(3): Show |
6 | HG00438.hp1 NA18981.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-4345T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659440 | |||||||
| chr18:45659599 | C | T | 7 | a0001c0004t0004g0148 a0001c0004t0004g0306 a0001c0004t0004g0307 others(4): Show |
7 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352-4186C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659599 | |||||||
| chr18:45659615 | C | A | 1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1352-4170C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659615 | |||||||
| chr18:45659616 | T | G | 208 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(205): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1352-4169T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659616 | |||||||
| chr18:45659634 | C | G | 2 | a0001c0002t0003g0071 a0005c0008t0003g0202 |
2 | HG00738.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1352-4151C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659634 | |||||||
| chr18:45659820 | T | C | 6 | a0004c0003t0001g0271 a0004c0003t0001g0272 a0004c0003t0001g0314 others(3): Show |
6 | HG00438.hp2 HG02083.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-3965T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45659820 | |||||||
| chr18:45659961 | C | CA | 141 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0004g0127 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1352-3808dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr18 | 45659961 | ||||||
| chr18:45660009 | T | C | 56 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(53): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1352-3776T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660009 | |||||||
| chr18:45660114 | T | C | 2 | a0011c0015t0004g0299 a0011c0015t0004g0300 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1352-3671T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660114 | |||||||
| chr18:45660138 | A | C | 64 | a0001c0002t0003g0092 a0001c0002t0003g0296 a0001c0002t0003g0328 others(61): Show |
67 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1352-3647A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660138 | |||||||
| chr18:45660192 | G | A | 1 | a0001c0004t0013g0322 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1352-3593G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660192 | |||||||
| chr18:45660204 | C | A | 1 | a0008c0025t0009g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1352-3581C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660204 | |||||||
| chr18:45660266 | A | G | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1352-3519A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660266 | |||||||
| chr18:45660275 | C | T | 216 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(213): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1352-3510C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660275 | |||||||
| chr18:45660297 | T | C | 128 | a0001c0004t0004g0127 a0002c0001t0001g0025 a0002c0001t0001g0037 others(125): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1352-3488T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660297 | |||||||
| chr18:45660632 | T | C | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-3153T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660632 | |||||||
| chr18:45660866 | G | A | 69 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(66): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1352-2919G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660866 | |||||||
| chr18:45660948 | A | G | 1 | a0015c0017t0002g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1352-2837A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45660948 | |||||||
| chr18:45661023 | T | C | 225 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(222): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1352-2762T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661023 | |||||||
| chr18:45661064 | C | T | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1352-2721C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661064 | |||||||
| chr18:45661109 | G | A | 1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1352-2676G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661109 | |||||||
| chr18:45661176 | T | C | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-2609T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661176 | |||||||
| chr18:45661191 | T | A | 1 | a0003c0006t0011g0169 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1352-2594T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661191 | |||||||
| chr18:45661197 | G | T | 3 | a0001c0023t0003g0374 a0003c0006t0002g0165 a0003c0006t0002g0305 |
3 | HG02257.hp1 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1352-2588G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661197 | |||||||
| chr18:45661215 | C | A | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1352-2570C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661215 | |||||||
| chr18:45661231 | G | C | 9 | a0001c0002t0004g0376 a0003c0006t0006g0185 a0004c0019t0001g0264 others(6): Show |
9 | HG00673.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1352-2554G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661231 | |||||||
| chr18:45661422 | C | T | 1 | a0004c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1352-2363C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661422 | |||||||
| chr18:45661490 | A | T | 1 | a0001c0002t0004g0376 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1352-2295A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661490 | |||||||
| chr18:45661759 | T | A | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-2026T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661759 | |||||||
| chr18:45661833 | C | T | 1 | a0008c0011t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1352-1952C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661833 | |||||||
| chr18:45661861 | A | G | 219 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(216): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1352-1924A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661861 | |||||||
| chr18:45661886 | C | T | 2 | a0008c0025t0009g0203 a0022c0027t0009g0187 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1352-1899C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661886 | |||||||
| chr18:45661908 | C | T | 216 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(213): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1352-1877C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45661908 | |||||||
| chr18:45662042 | C | T | 2 | a0003c0006t0002g0165 a0003c0006t0002g0305 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1352-1743C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662042 | |||||||
| chr18:45662146 | T | C | 2 | a0006c0007t0003g0149 a0006c0007t0003g0150 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1352-1639T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662146 | |||||||
| chr18:45662314 | G | A | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-1471G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662314 | |||||||
| chr18:45662362 | C | T | 6 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-1423C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662362 | |||||||
| chr18:45662428 | C | T | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-1357C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662428 | |||||||
| chr18:45662703 | G | A | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-1082G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662703 | |||||||
| chr18:45662871 | C | T | 11 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0007g0014 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1352-914C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45662871 | |||||||
| chr18:45663038 | C | G | 6 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-747C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45663038 | |||||||
| chr18:45663136 | G | A | 1 | a0006c0007t0003g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1352-649G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45663136 | |||||||
| chr18:45663260 | C | T | 4 | a0001c0004t0004g0251 a0005c0010t0004g0175 a0005c0010t0004g0176 others(1): Show |
4 | HG02572.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352-525C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45663260 | |||||||
| chr18:45663574 | G | A | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-211G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45663574 | |||||||
| chr18:45663714 | A | G | 293 | a0001c0002t0003g0092 a0001c0002t0003g0296 a0001c0002t0003g0328 others(290): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1352-71A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45663714 | |||||||
| chr18:45663774 | C | T | 1 | a0002c0001t0001g0347 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1352-11C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 10/19 | chr18 | 45663774 | |||||||
| chr18:45663917 | T | TC | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474+12dupC | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45663917 | ||||||
| chr18:45664142 | G | A | 1 | a0001c0004t0004g0351 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1474+235G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664142 | |||||||
| chr18:45664347 | C | T | 6 | a0001c0004t0004g0148 a0001c0004t0004g0306 a0001c0004t0004g0307 others(3): Show |
6 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474+440C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664347 | |||||||
| chr18:45664393 | G | A | 203 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(200): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1474+486G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664393 | |||||||
| chr18:45664546 | C | A | 5 | a0005c0008t0004g0171 a0008c0011t0001g0172 a0008c0011t0001g0174 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474+639C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664546 | |||||||
| chr18:45664553 | C | T | 3 | a0002c0001t0005g0333 a0002c0001t0005g0334 a0002c0001t0005g0337 |
3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1474+646C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664553 | |||||||
| chr18:45664793 | G | C | 63 | a0001c0002t0003g0092 a0001c0002t0003g0296 a0001c0002t0003g0328 others(60): Show |
66 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1474+886G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664793 | |||||||
| chr18:45664912 | C | T | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474+1005C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664912 | |||||||
| chr18:45664968 | G | A | 1 | a0003c0005t0002g0329 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1474+1061G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45664968 | |||||||
| chr18:45665172 | C | T | 1 | a0003c0005t0001g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1475-965C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665172 | |||||||
| chr18:45665207 | A | G | 6 | a0003c0006t0002g0165 a0003c0006t0002g0305 a0003c0006t0006g0185 others(3): Show |
6 | HG00673.hp2 HG02257.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1475-930A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665207 | |||||||
| chr18:45665243 | T | C | 1 | a0002c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1475-894T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665243 | |||||||
| chr18:45665350 | G | T | 225 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(222): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1475-787G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665350 | |||||||
| chr18:45665638 | C | T | 1 | a0006c0007t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1475-499C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665638 | |||||||
| chr18:45665661 | T | C | 208 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(205): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1475-476T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665661 | |||||||
| chr18:45665688 | C | CT | 104 | a0001c0002t0003g0040 a0001c0002t0003g0074 a0001c0002t0003g0101 others(101): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1475-421dupT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | C | CTT | 42 | a0001c0004t0004g0126 a0001c0004t0004g0127 a0001c0004t0004g0148 others(39): Show |
42 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1475-422_1475-421d others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | C | CTTTTTTT others(3): Show |
2 | a0003c0006t0001g0298 a0024c0034t0009g0191 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1475-430_1475-421d others(12): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | C | CTTTTTTT others(6): Show |
1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1475-433_1475-421d others(15): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | C | CTTTTTTT others(9): Show |
1 | a0004c0019t0001g0265 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1475-436_1475-421d others(18): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | C | CTTTTTTT others(10): Show |
1 | a0004c0019t0001g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1475-437_1475-421d others(19): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | CT | C | 8 | a0001c0002t0003g0283 a0001c0002t0003g0301 a0001c0002t0003g0345 others(5): Show |
8 | HG01257.hp2 HG02027.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475-421delT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | CTTTT | C | 20 | a0001c0004t0003g0051 a0001c0004t0004g0065 a0001c0004t0004g0320 others(17): Show |
20 | HG00642.hp2 HG01074.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1475-424_1475-421d others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | CTTTTT | C | 101 | a0001c0002t0003g0092 a0001c0002t0003g0296 a0001c0002t0003g0328 others(98): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1475-425_1475-421d others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665688 | CTTTTTT | C | 9 | a0001c0002t0004g0086 a0003c0018t0002g0135 a0004c0003t0001g0082 others(6): Show |
9 | HG01070.hp2 HG02486.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1475-426_1475-421d others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr18 | 45665688 | ||||||
| chr18:45665719 | T | C | 63 | a0001c0002t0003g0092 a0001c0002t0003g0296 a0001c0002t0003g0328 others(60): Show |
66 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1475-418T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665719 | |||||||
| chr18:45665739 | T | C | 296 | a0001c0002t0003g0092 a0001c0002t0003g0296 a0001c0002t0003g0328 others(293): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1475-398T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45665739 | |||||||
| chr18:45666021 | T | G | 208 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(205): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1475-116T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45666021 | |||||||
| chr18:45666050 | C | T | 1 | a0001c0004t0004g0276 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1475-87C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 11/19 | chr18 | 45666050 | |||||||
| chr18:45666342 | T | C | 3 | a0001c0004t0003g0051 a0005c0010t0003g0196 a0005c0010t0003g0234 |
3 | HG00642.hp2 HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1557+123T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | chr18 | 45666342 | |||||||
| chr18:45666364 | G | T | 207 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(204): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1557+145G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | chr18 | 45666364 | |||||||
| chr18:45666381 | TCA | T | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+165_1557+166d others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666381 | ||||||
| chr18:45666602 | T | TA | 6 | a0001c0002t0003g0010 a0001c0002t0003g0101 a0004c0003t0001g0122 others(3): Show |
7 | HG02155.hp2 HG02165.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558-320dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666602 | ||||||
| chr18:45666602 | T | TAA | 12 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0002c0001t0002g0068 others(9): Show |
13 | HG01256.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1558-321_1558-320d others(4): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666602 | ||||||
| chr18:45666602 | T | TAAA | 13 | a0001c0004t0004g0186 a0002c0001t0001g0095 a0002c0001t0001g0226 others(10): Show |
13 | HG00323.hp2 HG00741.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1558-322_1558-320d others(5): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666602 | ||||||
| chr18:45666602 | T | TAAAA | 152 | a0001c0004t0004g0020 a0001c0004t0004g0065 a0001c0004t0004g0098 others(149): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1558-323_1558-320d others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666602 | ||||||
| chr18:45666602 | T | TAAAAA | 41 | a0001c0002t0004g0376 a0001c0004t0003g0051 a0001c0004t0004g0126 others(38): Show |
44 | HG01109.hp1 HG01261.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.1558-324_1558-320d others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666602 | ||||||
| chr18:45666602 | T | TAAAAAA | 7 | a0002c0001t0001g0285 a0003c0006t0002g0165 a0003c0006t0002g0305 others(4): Show |
7 | HG00673.hp2 HG02074.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-325_1558-320d others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr18 | 45666602 | ||||||
| chr18:45666709 | G | A | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1558-226G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | chr18 | 45666709 | |||||||
| chr18:45666732 | G | A | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-203G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | chr18 | 45666732 | |||||||
| chr18:45666738 | CA | C | 9 | a0001c0002t0003g0283 a0001c0002t0003g0301 a0001c0002t0003g0345 others(6): Show |
9 | HG00621.hp1 HG02027.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-196delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | chr18 | 45666738 | |||||||
| chr18:45666814 | C | T | 225 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(222): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1558-121C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 12/19 | chr18 | 45666814 | |||||||
| chr18:45667248 | C | T | 1 | a0008c0011t0010g0195 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1717+154C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/19 | chr18 | 45667248 | |||||||
| chr18:45667392 | G | A | 6 | a0001c0002t0004g0376 a0005c0008t0004g0171 a0008c0011t0001g0172 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717+298G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/19 | chr18 | 45667392 | |||||||
| chr18:45667444 | G | C | 3 | a0002c0001t0001g0096 a0002c0001t0002g0358 a0002c0001t0002g0359 |
3 | HG02015.hp2 HG02132.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1717+350G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/19 | chr18 | 45667444 | |||||||
| chr18:45667566 | T | G | 225 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(222): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1718-267T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/19 | chr18 | 45667566 | |||||||
| chr18:45667742 | G | A | 1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1718-91G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/19 | chr18 | 45667742 | |||||||
| chr18:45667819 | C | T | 125 | a0002c0001t0001g0025 a0002c0001t0001g0037 a0002c0001t0001g0083 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1718-14C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 13/19 | chr18 | 45667819 | |||||||
| chr18:45668133 | T | C | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1907+111T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 14/19 | chr18 | 45668133 | |||||||
| chr18:45668199 | T | C | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1908-150T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 14/19 | chr18 | 45668199 | |||||||
| chr18:45668247 | C | T | 225 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(222): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1908-102C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 14/19 | chr18 | 45668247 | |||||||
| chr18:45668288 | A | C | 5 | a0003c0006t0002g0165 a0003c0006t0002g0305 a0003c0006t0006g0185 others(2): Show |
5 | HG00673.hp2 HG02257.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908-61A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 14/19 | chr18 | 45668288 | |||||||
| chr18:45668539 | T | C | 223 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(220): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2036+62T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668539 | |||||||
| chr18:45668544 | T | C | 204 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2036+67T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668544 | |||||||
| chr18:45668545 | G | A | 2 | a0008c0025t0009g0203 a0022c0027t0009g0187 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2036+68G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668545 | |||||||
| chr18:45668566 | A | T | 1 | a0005c0010t0013g0205 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2036+89A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668566 | |||||||
| chr18:45668613 | C | A | 204 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0065 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2036+136C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668613 | |||||||
| chr18:45668622 | A | C | 1 | a0012c0013t0022g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2036+145A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668622 | |||||||
| chr18:45668669 | A | T | 1 | a0006c0007t0004g0184 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2036+192A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668669 | |||||||
| chr18:45668733 | T | C | 1 | a0001c0004t0004g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2036+256T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668733 | |||||||
| chr18:45668929 | T | C | 1 | a0001c0002t0003g0377 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2037-377T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45668929 | |||||||
| chr18:45668979 | CA | C | 94 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(91): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2037-320delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr18 | 45668979 | ||||||
| chr18:45669175 | C | T | 1 | a0014c0020t0004g0274 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2037-131C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45669175 | |||||||
| chr18:45669195 | C | A | 1 | a0002c0001t0002g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2037-111C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45669195 | |||||||
| chr18:45669268 | G | A | 1 | a0003c0005t0002g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2037-38G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45669268 | |||||||
| chr18:45669283 | A | G | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2037-23A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 15/19 | chr18 | 45669283 | |||||||
| chr18:45669668 | G | A | 59 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0098 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2229+170G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669668 | |||||||
| chr18:45669707 | A | G | 2 | a0003c0006t0002g0067 a0003c0006t0002g0318 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2229+209A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669707 | |||||||
| chr18:45669728 | G | A | 58 | a0001c0004t0003g0051 a0001c0004t0004g0020 a0001c0004t0004g0098 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.2229+230G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669728 | |||||||
| chr18:45669786 | A | G | 1 | a0008c0011t0002g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2229+288A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669786 | |||||||
| chr18:45669840 | T | C | 213 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0003g0051 others(210): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2229+342T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669840 | |||||||
| chr18:45669874 | T | G | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.2229+376T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669874 | |||||||
| chr18:45669903 | C | T | 1 | a0001c0002t0004g0360 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2229+405C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669903 | |||||||
| chr18:45669904 | G | A | 8 | a0004c0003t0001g0271 a0004c0003t0001g0272 a0004c0003t0001g0302 others(5): Show |
8 | HG00438.hp2 HG02083.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2229+406G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45669904 | |||||||
| chr18:45670110 | C | G | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.2229+612C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670110 | |||||||
| chr18:45670144 | C | A | 4 | a0001c0002t0003g0054 a0001c0002t0003g0073 a0001c0002t0003g0074 others(1): Show |
4 | HG00438.hp1 NA18981.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2229+646C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670144 | |||||||
| chr18:45670145 | G | A | 9 | a0002c0001t0005g0006 a0002c0001t0005g0039 a0002c0001t0005g0100 others(6): Show |
11 | HG01358.hp1 HG01433.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.2229+647G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670145 | |||||||
| chr18:45670187 | GC | G | 64 | a0001c0004t0004g0020 a0001c0004t0004g0098 a0001c0004t0004g0107 others(61): Show |
66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2229+690delC | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670187 | |||||||
| chr18:45670189 | T | G | 64 | a0001c0004t0004g0020 a0001c0004t0004g0098 a0001c0004t0004g0107 others(61): Show |
66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2229+691T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670189 | |||||||
| chr18:45670208 | T | C | 5 | a0005c0008t0004g0171 a0008c0011t0001g0172 a0008c0011t0001g0174 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2229+710T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670208 | |||||||
| chr18:45670248 | TATAAC | T | 3 | a0003c0006t0006g0185 a0004c0019t0001g0264 a0004c0019t0001g0265 |
3 | HG00673.hp2 HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.2229+752_2229+756d others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr18 | 45670248 | ||||||
| chr18:45670250 | T | C | 1 | a0003c0005t0017g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2229+752T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670250 | |||||||
| chr18:45670414 | A | G | 152 | a0001c0002t0003g0092 a0001c0002t0004g0376 a0001c0002t0008g0143 others(149): Show |
162 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.2229+916A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670414 | |||||||
| chr18:45670436 | C | A | 1 | a0002c0001t0002g0035 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2229+938C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670436 | |||||||
| chr18:45670443 | C | T | 13 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0002g0090 others(10): Show |
14 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2229+945C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670443 | |||||||
| chr18:45670551 | C | T | 13 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0002g0090 others(10): Show |
14 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2229+1053C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670551 | |||||||
| chr18:45670556 | T | C | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2229+1058T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670556 | |||||||
| chr18:45670697 | G | A | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2229+1199G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45670697 | |||||||
| chr18:45671013 | C | A | 1 | a0004c0003t0001g0162 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2229+1515C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671013 | |||||||
| chr18:45671090 | A | G | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2229+1592A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671090 | |||||||
| chr18:45671233 | A | C | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2230-1667A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671233 | |||||||
| chr18:45671284 | C | T | 1 | a0002c0001t0001g0037 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2230-1616C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671284 | |||||||
| chr18:45671301 | G | C | 1 | a0004c0003t0001g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2230-1599G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671301 | |||||||
| chr18:45671456 | G | A | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2230-1444G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671456 | |||||||
| chr18:45671487 | C | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2230-1413C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671487 | |||||||
| chr18:45671490 | C | G | 79 | a0001c0002t0004g0376 a0003c0006t0006g0185 a0004c0003t0001g0003 others(76): Show |
86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2230-1410C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671490 | |||||||
| chr18:45671627 | C | A | 4 | a0003c0006t0001g0298 a0005c0008t0004g0171 a0008c0011t0001g0172 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2230-1273C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671627 | |||||||
| chr18:45671672 | C | A | 1 | a0004c0003t0001g0341 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2230-1228C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671672 | |||||||
| chr18:45671753 | C | T | 2 | a0001c0004t0004g0107 a0001c0004t0004g0118 |
2 | NA18953.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2230-1147C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671753 | |||||||
| chr18:45671808 | G | A | 77 | a0004c0003t0001g0003 a0004c0003t0001g0011 a0004c0003t0001g0029 others(74): Show |
84 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2230-1092G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671808 | |||||||
| chr18:45671826 | C | A | 77 | a0004c0003t0001g0003 a0004c0003t0001g0011 a0004c0003t0001g0029 others(74): Show |
84 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2230-1074C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671826 | |||||||
| chr18:45671902 | G | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2230-998G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45671902 | |||||||
| chr18:45672052 | T | A | 2 | a0001c0002t0004g0376 a0006c0007t0004g0170 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2230-848T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672052 | |||||||
| chr18:45672088 | C | T | 4 | a0014c0020t0004g0274 a0014c0020t0004g0275 a0014c0020t0004g0280 others(1): Show |
4 | HG01243.hp2 HG02015.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2230-812C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672088 | |||||||
| chr18:45672101 | G | A | 1 | a0004c0003t0020g0026 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2230-799G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672101 | |||||||
| chr18:45672399 | T | C | 245 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(242): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2230-501T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672399 | |||||||
| chr18:45672454 | G | A | 13 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0002g0090 others(10): Show |
14 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2230-446G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672454 | |||||||
| chr18:45672501 | C | G | 1 | a0002c0001t0002g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2230-399C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672501 | |||||||
| chr18:45672529 | C | CA | 25 | a0001c0004t0004g0364 a0001c0004t0004g0366 a0001c0004t0004g0367 others(22): Show |
26 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(23): Show |
intron_variant | MODIFIER | c.2230-355dupA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr18 | 45672529 | ||||||
| chr18:45672529 | CA | C | 78 | a0002c0001t0002g0019 a0003c0006t0006g0185 a0004c0003t0001g0003 others(75): Show |
85 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2230-355delA | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr18 | 45672529 | ||||||
| chr18:45672614 | C | T | 86 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(83): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.2230-286C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672614 | |||||||
| chr18:45672664 | C | T | 106 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(103): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2230-236C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672664 | |||||||
| chr18:45672811 | G | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2230-89G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672811 | |||||||
| chr18:45672821 | A | G | 377 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(374): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.2230-79A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672821 | |||||||
| chr18:45672886 | T | G | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2230-14T>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 16/19 | chr18 | 45672886 | |||||||
| chr18:45673086 | A | G | 1 | a0001c0023t0003g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2377+39A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673086 | |||||||
| chr18:45673135 | C | T | 168 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(165): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2377+88C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673135 | |||||||
| chr18:45673330 | A | G | 106 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(103): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2377+283A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673330 | |||||||
| chr18:45673335 | A | G | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2377+288A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673335 | |||||||
| chr18:45673375 | G | A | 4 | a0001c0004t0004g0227 a0001c0004t0004g0260 a0003c0006t0002g0165 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2378-308G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673375 | |||||||
| chr18:45673395 | C | T | 87 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(84): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2378-288C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673395 | |||||||
| chr18:45673498 | T | C | 6 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2378-185T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673498 | |||||||
| chr18:45673577 | A | G | 1 | a0004c0003t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2378-106A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673577 | |||||||
| chr18:45673677 | T | C | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.2378-6T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 17/19 | chr18 | 45673677 | |||||||
| chr18:45673858 | G | T | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2512+41G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45673858 | |||||||
| chr18:45673954 | C | T | 1 | a0005c0008t0003g0207 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2512+137C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45673954 | |||||||
| chr18:45674104 | C | T | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2512+287C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674104 | |||||||
| chr18:45674196 | G | A | 13 | a0001c0004t0004g0126 a0001c0004t0004g0148 a0001c0004t0004g0306 others(10): Show |
13 | HG01081.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2512+379G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674196 | |||||||
| chr18:45674317 | A | T | 2 | a0001c0002t0004g0376 a0006c0007t0004g0170 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2512+500A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674317 | |||||||
| chr18:45674410 | C | A | 126 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(123): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.2512+593C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674410 | |||||||
| chr18:45674410 | C | T | 1 | a0004c0003t0001g0323 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2512+593C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674410 | |||||||
| chr18:45674521 | C | T | 2 | a0008c0011t0010g0194 a0008c0011t0010g0195 |
2 | NA18940.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.2512+704C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674521 | |||||||
| chr18:45674695 | C | T | 2 | a0003c0006t0002g0067 a0003c0006t0002g0318 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2512+878C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674695 | |||||||
| chr18:45674727 | T | C | 1 | a0004c0003t0001g0289 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2512+910T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674727 | |||||||
| chr18:45674739 | T | C | 1 | a0001c0004t0004g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2512+922T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674739 | |||||||
| chr18:45674742 | G | T | 2 | a0001c0002t0004g0376 a0006c0007t0004g0170 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2512+925G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674742 | |||||||
| chr18:45674755 | G | A | 1 | a0001c0022t0004g0339 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2512+938G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674755 | |||||||
| chr18:45674775 | A | G | 1 | a0008c0011t0010g0195 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2512+958A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674775 | |||||||
| chr18:45674908 | A | T | 13 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0002g0090 others(10): Show |
14 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2512+1091A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674908 | |||||||
| chr18:45674918 | C | T | 2 | a0011c0015t0004g0299 a0011c0015t0004g0300 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2512+1101C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674918 | |||||||
| chr18:45674956 | G | A | 1 | a0008c0011t0002g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2512+1139G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674956 | |||||||
| chr18:45674973 | C | T | 4 | a0003c0006t0001g0298 a0005c0008t0004g0171 a0008c0011t0001g0172 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2512+1156C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45674973 | |||||||
| chr18:45675020 | G | A | 4 | a0001c0004t0004g0251 a0005c0010t0004g0175 a0005c0010t0004g0176 others(1): Show |
4 | HG02572.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2512+1203G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675020 | |||||||
| chr18:45675027 | T | C | 6 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2512+1210T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675027 | |||||||
| chr18:45675035 | C | T | 8 | a0004c0003t0001g0094 a0004c0003t0001g0271 a0004c0003t0001g0272 others(5): Show |
8 | HG00438.hp2 HG02074.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.2512+1218C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675035 | |||||||
| chr18:45675199 | C | A | 1 | a0004c0003t0001g0122 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2512+1382C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675199 | |||||||
| chr18:45675451 | G | T | 203 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(200): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.2512+1634G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675451 | |||||||
| chr18:45675501 | G | T | 3 | a0003c0033t0002g0134 a0015c0017t0002g0042 a0015c0017t0002g0043 |
3 | HG02723.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2512+1684G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675501 | |||||||
| chr18:45675685 | C | A | 1 | a0008c0011t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2512+1868C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675685 | |||||||
| chr18:45675685 | C | CTA | 11 | a0001c0004t0004g0307 a0002c0001t0002g0015 a0002c0001t0002g0044 others(8): Show |
11 | HG01081.hp1 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.2512+1892_2512+189 others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675685 | ||||||
| chr18:45675685 | C | CTATA | 4 | a0002c0001t0002g0128 a0002c0001t0006g0111 a0002c0001t0006g0303 others(1): Show |
4 | HG01255.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2512+1890_2512+189 others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675685 | ||||||
| chr18:45675685 | C | CTATATA | 7 | a0002c0001t0002g0129 a0002c0001t0002g0130 a0002c0001t0006g0080 others(4): Show |
7 | HG01074.hp1 HG01109.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2512+1888_2512+189 others(10): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675685 | ||||||
| chr18:45675685 | C | CTATATAT others(3): Show |
3 | a0004c0003t0020g0026 a0007c0009t0001g0105 a0013c0016t0001g0230 |
3 | HG03831.hp2 NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2512+1884_2512+189 others(14): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675685 | ||||||
| chr18:45675694 | T | TATATATC others(81): Show |
1 | a0005c0010t0004g0176 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2512+1883_2512+188 others(92): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675694 | ||||||
| chr18:45675694 | T | TATATATC others(81): Show |
2 | a0001c0004t0004g0251 a0005c0010t0004g0175 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2512+1883_2512+188 others(92): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675694 | ||||||
| chr18:45675694 | T | TATATATC others(119): Show |
1 | a0005c0010t0004g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2512+1883_2512+188 others(130): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675694 | ||||||
| chr18:45675701 | A | C | 2 | a0001c0002t0004g0376 a0006c0007t0004g0170 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2512+1884A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675701 | |||||||
| chr18:45675701 | ATATATAT others(6): Show |
A | 2 | a0011c0015t0004g0299 a0011c0015t0004g0300 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2512+1886_2512+189 others(17): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675701 | ||||||
| chr18:45675704 | TATATA | T | 5 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(2): Show |
5 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2512+1888_2512+189 others(9): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675704 | |||||||
| chr18:45675706 | TATA | T | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2512+1890_2512+189 others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675706 | |||||||
| chr18:45675707 | A | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2512+1890A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675707 | |||||||
| chr18:45675707 | ATATT | A | 32 | a0001c0002t0003g0054 a0001c0002t0004g0086 a0001c0002t0004g0087 others(29): Show |
34 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2512+1892_2512+189 others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675707 | ||||||
| chr18:45675707 | ATATTT | A | 63 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(60): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2512+1892_2512+189 others(9): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675707 | ||||||
| chr18:45675709 | A | ATATATAT | 49 | a0004c0003t0001g0011 a0004c0003t0001g0075 a0004c0003t0001g0077 others(46): Show |
51 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2512+1893_2512+189 others(11): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | ATATATAT others(2): Show |
11 | a0003c0005t0001g0072 a0003c0005t0001g0116 a0004c0003t0001g0029 others(8): Show |
11 | HG01099.hp2 HG01106.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2512+1893_2512+189 others(13): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | ATATATAT others(4): Show |
4 | a0003c0005t0001g0379 a0004c0003t0001g0003 a0004c0003t0001g0302 others(1): Show |
6 | HG00673.hp1 NA18747.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.2512+1893_2512+189 others(15): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | ATATATAT others(8): Show |
1 | a0010c0014t0001g0216 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(19): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | ATATATAT others(9): Show |
1 | a0008c0011t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(20): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | ATATATAT others(3): Show |
1 | a0008c0011t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(14): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | ATATATAT others(5): Show |
1 | a0003c0006t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(16): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | A | T | 2 | a0001c0002t0008g0311 a0003c0006t0006g0185 |
2 | HG02738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2512+1892A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675709 | |||||||
| chr18:45675709 | ATT | A | 37 | a0001c0002t0003g0092 a0001c0004t0003g0051 a0001c0004t0004g0351 others(34): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.2512+1911_2512+191 others(6): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | ATTT | A | 9 | a0001c0002t0003g0005 a0001c0002t0003g0097 a0002c0001t0002g0064 others(6): Show |
9 | HG01109.hp1 HG01433.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2512+1910_2512+191 others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | ATTTT | A | 29 | a0001c0002t0003g0133 a0001c0002t0004g0360 a0001c0004t0004g0020 others(26): Show |
29 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2512+1909_2512+191 others(8): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675709 | ATTTTT | A | 7 | a0001c0002t0003g0031 a0001c0002t0003g0071 a0001c0002t0003g0076 others(4): Show |
7 | HG01346.hp1 HG03041.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2512+1908_2512+191 others(9): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675709 | ||||||
| chr18:45675710 | T | TA | 13 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0004t0004g0126 others(10): Show |
14 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.2512+1893_2512+189 others(5): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675710 | |||||||
| chr18:45675710 | T | TATA | 3 | a0003c0033t0002g0134 a0015c0017t0002g0042 a0015c0017t0002g0043 |
3 | HG02723.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2512+1893_2512+189 others(7): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675710 | |||||||
| chr18:45675710 | T | TATATA | 3 | a0002c0001t0006g0125 a0002c0001t0006g0166 a0003c0005t0007g0048 |
3 | HG02895.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2512+1893_2512+189 others(9): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675710 | |||||||
| chr18:45675710 | T | TATATATA others(4): Show |
1 | a0007c0009t0001g0109 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(15): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675710 | |||||||
| chr18:45675710 | T | TATCTATA others(44): Show |
1 | a0006c0007t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(55): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675710 | |||||||
| chr18:45675710 | T | TATCTATA others(44): Show |
1 | a0001c0002t0004g0376 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2512+1893_2512+189 others(55): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675710 | |||||||
| chr18:45675711 | T | A | 71 | a0001c0004t0004g0127 a0001c0004t0004g0148 a0001c0004t0004g0306 others(68): Show |
72 | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.2512+1894T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675711 | |||||||
| chr18:45675712 | T | A | 22 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(19): Show |
23 | HG01070.hp1 HG01891.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.2512+1895T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675712 | |||||||
| chr18:45675713 | T | A | 84 | a0001c0002t0003g0092 a0001c0004t0003g0051 a0001c0004t0004g0127 others(81): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2512+1896T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675713 | |||||||
| chr18:45675714 | T | A | 20 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0001c0002t0004g0376 others(17): Show |
21 | HG01070.hp1 HG01109.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.2512+1897T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675714 | |||||||
| chr18:45675715 | T | A | 6 | a0001c0002t0003g0092 a0001c0004t0023g0188 a0002c0001t0002g0225 others(3): Show |
6 | HG00621.hp2 HG01261.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.2512+1898T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675715 | |||||||
| chr18:45675716 | T | A | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2512+1899T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675716 | |||||||
| chr18:45675718 | T | A | 2 | a0015c0017t0002g0042 a0015c0017t0002g0043 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2512+1901T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675718 | |||||||
| chr18:45675738 | AG | A | 112 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(109): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2512+1924delG | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45675738 | ||||||
| chr18:45675864 | C | T | 13 | a0001c0002t0004g0242 a0001c0002t0004g0309 a0003c0005t0002g0090 others(10): Show |
14 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2512+2047C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45675864 | |||||||
| chr18:45676214 | G | A | 1 | a0002c0001t0005g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2512+2397G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45676214 | |||||||
| chr18:45676388 | C | T | 1 | a0001c0004t0004g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2512+2571C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45676388 | |||||||
| chr18:45676412 | T | C | 1 | a0001c0002t0003g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2513-2563T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45676412 | |||||||
| chr18:45676639 | C | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2513-2336C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45676639 | |||||||
| chr18:45676866 | C | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2513-2109C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45676866 | |||||||
| chr18:45677089 | C | T | 5 | a0001c0004t0004g0020 a0001c0004t0004g0186 a0001c0004t0004g0261 others(2): Show |
5 | HG00099.hp2 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2513-1886C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677089 | |||||||
| chr18:45677099 | C | T | 287 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(284): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2513-1876C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677099 | |||||||
| chr18:45677113 | C | T | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2513-1862C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677113 | |||||||
| chr18:45677200 | T | A | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2513-1775T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677200 | |||||||
| chr18:45677351 | C | A | 2 | a0011c0015t0004g0299 a0011c0015t0004g0300 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2513-1624C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677351 | |||||||
| chr18:45677366 | C | G | 1 | a0005c0010t0004g0257 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2513-1609C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677366 | |||||||
| chr18:45677380 | G | A | 81 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.2513-1595G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677380 | |||||||
| chr18:45677507 | G | T | 3 | a0001c0002t0003g0115 a0001c0002t0003g0293 a0001c0002t0003g0294 |
3 | NA18946.hp2 NA18955.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2513-1468G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677507 | |||||||
| chr18:45677696 | C | T | 4 | a0001c0004t0004g0251 a0005c0010t0004g0175 a0005c0010t0004g0176 others(1): Show |
4 | HG02572.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-1279C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677696 | |||||||
| chr18:45677811 | G | A | 2 | a0001c0002t0003g0078 a0001c0002t0003g0097 |
2 | NA19009.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2513-1164G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677811 | |||||||
| chr18:45677937 | G | T | 12 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(9): Show |
13 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2513-1038G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45677937 | |||||||
| chr18:45678011 | A | G | 9 | a0001c0002t0004g0376 a0001c0004t0004g0251 a0005c0010t0004g0175 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2513-964A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678011 | |||||||
| chr18:45678050 | C | T | 1 | a0010c0014t0001g0216 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2513-925C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678050 | |||||||
| chr18:45678117 | T | C | 374 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(371): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.2513-858T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678117 | |||||||
| chr18:45678396 | C | T | 2 | a0001c0002t0004g0376 a0006c0007t0004g0170 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2513-579C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678396 | |||||||
| chr18:45678399 | G | A | 9 | a0001c0004t0004g0126 a0001c0004t0004g0148 a0001c0004t0004g0306 others(6): Show |
9 | HG01081.hp2 HG02257.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2513-576G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678399 | |||||||
| chr18:45678653 | G | A | 1 | a0002c0001t0006g0111 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2513-322G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678653 | |||||||
| chr18:45678784 | T | C | 2 | a0008c0025t0009g0203 a0022c0027t0009g0187 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2513-191T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678784 | |||||||
| chr18:45678790 | A | G | 3 | a0008c0025t0009g0203 a0022c0027t0009g0187 a0024c0034t0009g0191 |
3 | HG02922.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2513-185A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678790 | |||||||
| chr18:45678954 | C | CT | 121 | a0001c0004t0003g0051 a0001c0004t0004g0340 a0002c0001t0002g0009 others(118): Show |
127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
splice_region_variant&intron_variant | LOW | c.2513-5dupT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45678954 | ||||||
| chr18:45678954 | C | CTTT | 90 | a0002c0001t0001g0025 a0002c0001t0001g0083 a0002c0001t0001g0084 others(87): Show |
97 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
splice_region_variant&intron_variant | LOW | c.2513-7_2513-5dupTT others(1): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45678954 | ||||||
| chr18:45678954 | CT | C | 13 | a0001c0002t0004g0242 a0001c0004t0004g0126 a0001c0004t0004g0127 others(10): Show |
13 | HG01081.hp2 HG02257.hp2 HG02572.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.2513-5delT | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr18 | 45678954 | ||||||
| chr18:45678970 | T | C | 2 | a0001c0004t0016g0259 a0005c0010t0014g0012 |
3 | HG01884.hp1 HG02486.hp2 HG02965.hp1 |
splice_region_variant&intron_variant | LOW | c.2513-5T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 18/19 | chr18 | 45678970 | |||||||
| chr18:45679061 | C | T | 2 | a0002c0001t0002g0286 a0002c0001t0002g0287 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2562+37C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679061 | |||||||
| chr18:45679159 | T | A | 10 | a0001c0004t0004g0126 a0001c0004t0004g0127 a0001c0004t0004g0148 others(7): Show |
10 | HG01081.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2562+135T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679159 | |||||||
| chr18:45679285 | G | A | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2562+261G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679285 | |||||||
| chr18:45679437 | A | T | 10 | a0002c0001t0005g0006 a0002c0001t0005g0039 a0002c0001t0005g0100 others(7): Show |
12 | HG00733.hp2 HG01433.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+413A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679437 | |||||||
| chr18:45679449 | C | T | 2 | a0001c0004t0004g0277 a0001c0004t0004g0278 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2562+425C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679449 | |||||||
| chr18:45679482 | C | T | 1 | a0010c0014t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2562+458C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679482 | |||||||
| chr18:45679483 | G | A | 74 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(71): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.2562+459G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679483 | |||||||
| chr18:45679495 | G | A | 1 | a0003c0005t0006g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2562+471G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679495 | |||||||
| chr18:45679501 | C | T | 2 | a0001c0004t0004g0126 a0001c0004t0004g0127 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2562+477C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679501 | |||||||
| chr18:45679522 | G | A | 2 | a0001c0004t0004g0126 a0001c0004t0004g0127 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2562+498G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679522 | |||||||
| chr18:45679592 | T | C | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2562+568T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679592 | |||||||
| chr18:45679657 | A | C | 367 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(364): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.2562+633A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679657 | |||||||
| chr18:45679745 | G | A | 1 | a0011c0015t0003g0055 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2562+721G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679745 | |||||||
| chr18:45679819 | C | T | 1 | a0001c0004t0004g0369 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2562+795C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679819 | |||||||
| chr18:45679871 | G | A | 2 | a0005c0008t0003g0256 a0005c0008t0003g0258 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2562+847G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45679871 | |||||||
| chr18:45680120 | G | A | 2 | a0001c0002t0004g0376 a0006c0007t0004g0170 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2562+1096G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680120 | |||||||
| chr18:45680352 | T | C | 24 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(21): Show |
25 | HG01081.hp2 HG01496.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2562+1328T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680352 | |||||||
| chr18:45680389 | C | T | 1 | a0004c0003t0005g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2562+1365C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680389 | |||||||
| chr18:45680419 | T | C | 3 | a0005c0008t0004g0171 a0008c0011t0001g0172 a0008c0011t0001g0174 |
3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2562+1395T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680419 | |||||||
| chr18:45680460 | A | C | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2562+1436A>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680460 | |||||||
| chr18:45680492 | C | T | 3 | a0002c0001t0002g0034 a0002c0001t0002g0062 a0002c0001t0002g0326 |
3 | NA18948.hp1 NA18970.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2562+1468C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680492 | |||||||
| chr18:45680527 | A | T | 11 | a0001c0004t0004g0126 a0001c0004t0004g0127 a0001c0004t0004g0148 others(8): Show |
11 | HG01081.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2562+1503A>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680527 | |||||||
| chr18:45680543 | T | C | 1 | a0003c0006t0006g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2562+1519T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680543 | |||||||
| chr18:45680607 | C | T | 74 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(71): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.2562+1583C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680607 | |||||||
| chr18:45680735 | G | A | 154 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2563-1584G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680735 | |||||||
| chr18:45680792 | C | A | 96 | a0002c0001t0001g0025 a0002c0001t0001g0037 a0002c0001t0001g0083 others(93): Show |
103 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2563-1527C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680792 | |||||||
| chr18:45680938 | C | T | 73 | a0003c0005t0001g0072 a0003c0005t0001g0116 a0003c0005t0001g0379 others(70): Show |
80 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2563-1381C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680938 | |||||||
| chr18:45680982 | C | A | 7 | a0001c0004t0004g0251 a0005c0008t0004g0171 a0005c0010t0004g0175 others(4): Show |
7 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2563-1337C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680982 | |||||||
| chr18:45680986 | G | A | 119 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(116): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.2563-1333G>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45680986 | |||||||
| chr18:45681007 | C | A | 13 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(10): Show |
13 | HG01496.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2563-1312C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681007 | |||||||
| chr18:45681038 | TCTGAGGT others(318): Show |
T | 358 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(355): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2563-1269_2563-945 others(3): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr18 | 45681038 | ||||||
| chr18:45681044 | G | GTTTTTTT others(9): Show |
1 | a0015c0017t0002g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2563-1253_2563-123 others(20): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr18 | 45681044 | ||||||
| chr18:45681044 | G | GTTTTTTT others(15): Show |
1 | a0015c0017t0002g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2563-1259_2563-123 others(26): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr18 | 45681044 | ||||||
| chr18:45681044 | GTTTTTTT others(13): Show |
G | 1 | a0024c0034t0009g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2563-1257_2563-123 others(24): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr18 | 45681044 | ||||||
| chr18:45681044 | GTTTTTTT others(14): Show |
G | 8 | a0002c0001t0006g0080 a0002c0001t0006g0111 a0002c0001t0006g0125 others(5): Show |
8 | HG01109.hp2 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2563-1258_2563-123 others(25): Show |
SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr18 | 45681044 | ||||||
| chr18:45681383 | T | A | 1 | a0001c0002t0003g0097 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2563-936T>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681383 | |||||||
| chr18:45681461 | C | T | 73 | a0001c0002t0003g0250 a0001c0002t0004g0086 a0001c0002t0004g0087 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.2563-858C>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681461 | |||||||
| chr18:45681511 | C | G | 1 | a0001c0002t0004g0242 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2563-808C>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681511 | |||||||
| chr18:45681618 | T | C | 13 | a0001c0002t0008g0143 a0001c0002t0008g0249 a0001c0002t0008g0255 others(10): Show |
13 | HG01496.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2563-701T>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681618 | |||||||
| chr18:45681823 | C | A | 377 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0002t0003g0010 others(374): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.2563-496C>A | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681823 | |||||||
| chr18:45681924 | G | T | 12 | a0001c0004t0004g0126 a0001c0004t0004g0127 a0001c0004t0004g0148 others(9): Show |
13 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2563-395G>T | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681924 | |||||||
| chr18:45681989 | G | C | 1 | a0002c0001t0002g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2563-330G>C | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45681989 | |||||||
| chr18:45682076 | A | G | 1 | a0004c0003t0005g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2563-243A>G | SLC14A2 | ENSG00000132874.15 | transcript | ENST00000255226.11 | protein_coding | 19/19 | chr18 | 45682076 |