Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6768 |
| ensemblid | ENSG00000149418.11 |
| hgncid | 11344 |
| symbol | ST14 |
| name | ST14 transmembrane serine protease matriptase |
| refseq_nuc | NM_021978.4 |
| refseq_prot | NP_068813.1 |
| ensembl_nuc | ENST00000278742.6 |
| ensembl_prot | ENSP00000278742.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 130159782 |
| end | 130210362 |
| strand | + |
| ver | v1.2 |
| region | chr11:130159782-130210362 |
| region5000 | chr11:130154782-130215362 |
| regionname0 | ST14_chr11_130159782_130210362 |
| regionname5000 | ST14_chr11_130154782_130215362 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 855 | 221 | 43 | 42 | 98 | 11 | 25 | 74 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0002 | 0/0 | 855 | 29 | 27 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0003 | 0/0 | 855 | 13 | 0 | 10 | 1 | 1 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0004 | 0/0 | 855 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0005 | 0/0 | 855 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0006 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0007 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0008 | 0/0 | 855 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0009 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0010 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0011 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0012 | 0/0 | 855 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| a0013 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | MGSDR others(850): Show |
chr11 | 130154782 | 130215362 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2565 | 120 | 12 | 24 | 61 | 7 | 16 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0002 | 0/1 | 2565 | 41 | 7 | 6 | 20 | 3 | 4 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0003 | 1/0 | 2565 | 36 | 9 | 7 | 14 | 1 | 4 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0007 | 0/0 | 2565 | 9 | 9 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0010 | 0/0 | 2565 | 3 | 1 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0012 | 0/0 | 2565 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0016 | 0/0 | 2565 | 2 | 1 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0019 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0020 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0023 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0025 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0026 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0028 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0031 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0001c0035 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0002c0004 | 0/0 | 2565 | 16 | 14 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0002c0006 | 0/0 | 2565 | 11 | 11 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0002c0011 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0003c0005 | 0/0 | 2565 | 12 | 0 | 9 | 1 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0003c0017 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0004c0008 | 0/0 | 2565 | 7 | 6 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0004c0013 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0004c0027 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0004c0030 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0004c0033 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0005c0009 | 0/0 | 2565 | 6 | 5 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0006c0015 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0007c0014 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0008c0022 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0008c0034 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0009c0032 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0010c0018 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0011c0029 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0012c0021 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 | ||
| a0013c0024 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | ATGGG others(2560): Show |
chr11 | 130154782 | 130215362 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3305 | 41 | 3 | 7 | 27 | 2 | 2 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0001t0002 | 0/0 | 3305 | 75 | 6 | 17 | 33 | 5 | 14 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0001t0003 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0001t0004 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0001t0008 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0002t0001 | 0/1 | 3305 | 30 | 7 | 3 | 17 | 0 | 2 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0002t0002 | 0/0 | 3305 | 10 | 0 | 2 | 3 | 3 | 2 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0002t0003 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0003t0001 | 1/0 | 3305 | 23 | 5 | 7 | 6 | 1 | 3 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0003t0002 | 0/0 | 3305 | 9 | 0 | 0 | 8 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0003t0003 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0003t0005 | 0/0 | 3305 | 3 | 3 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0007t0001 | 0/0 | 3305 | 5 | 5 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0007t0002 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0007t0003 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0010t0001 | 0/0 | 3305 | 2 | 1 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0010t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0012t0002 | 0/0 | 3305 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0016t0002 | 0/0 | 3305 | 2 | 1 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0019t0003 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0020t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0023t0001 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0025t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0026t0002 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0028t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0031t0007 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0001c0035t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0002c0004t0001 | 0/0 | 3305 | 3 | 2 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0002c0004t0002 | 0/0 | 3305 | 13 | 12 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0002c0006t0001 | 0/0 | 3305 | 10 | 10 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0002c0006t0006 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0002c0011t0003 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0003c0005t0001 | 0/0 | 3305 | 11 | 0 | 9 | 0 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0003c0005t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0003c0017t0001 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0008t0001 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0008t0004 | 0/0 | 3305 | 5 | 4 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0013t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0013t0004 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0027t0002 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0030t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0004c0033t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0005c0009t0002 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0005c0009t0003 | 0/0 | 3305 | 4 | 3 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0006c0015t0004 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0007c0014t0001 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0008c0022t0001 | 0/0 | 3305 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0008c0034t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0009c0032t0002 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0010c0018t0002 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0011c0029t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0012c0021t0002 | 0/0 | 3305 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| a0013c0024t0001 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | GTGAG others(3300): Show |
chr11 | 130154782 | 130215362 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0010t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0010t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0010t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0012t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0012t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0016t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0016t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0019t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0020t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0023t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0025t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0026t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0028t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0031t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0035t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0011t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0011t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0017t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0013t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0013t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0027t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0030t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0033t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0006c0015t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0006c0015t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0007c0014t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0007c0014t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0008c0022t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0008c0034t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0009c0032t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0010c0018t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0011c0029t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0012c0021t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0013c0024t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | GBR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0185 | EUR | GBR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00323 | hp1 | a0003 | c0005 | t0001 | g0125 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0267 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00423 | hp2 | a0001 | c0010 | t0001 | g0088 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00597 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00639 | hp1 | a0003 | c0005 | t0001 | g0121 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0263 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0195 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00735 | hp2 | a0001 | c0016 | t0002 | g0106 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0049 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01074 | hp1 | a0009 | c0032 | t0002 | g0070 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01074 | hp2 | a0001 | c0023 | t0001 | g0232 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0194 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01099 | hp2 | a0001 | c0026 | t0002 | g0135 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01106 | hp1 | a0003 | c0005 | t0001 | g0008 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01109 | hp1 | a0004 | c0008 | t0004 | g0238 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0075 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0206 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01243 | hp2 | a0003 | c0005 | t0001 | g0119 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0052 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01255 | hp2 | a0003 | c0005 | t0001 | g0027 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01257 | hp2 | a0001 | c0012 | t0002 | g0136 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01261 | hp2 | a0005 | c0009 | t0003 | g0221 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01346 | hp1 | a0001 | c0031 | t0007 | g0030 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01496 | hp1 | a0002 | c0004 | t0002 | g0012 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0013 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0013 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0041 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0226 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01891 | hp2 | a0002 | c0006 | t0001 | g0214 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01928 | hp2 | a0003 | c0005 | t0001 | g0126 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01934 | hp1 | a0003 | c0005 | t0001 | g0080 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01934 | hp2 | a0003 | c0005 | t0001 | g0124 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0123 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01981 | hp1 | a0010 | c0018 | t0002 | g0020 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01981 | hp2 | a0003 | c0005 | t0001 | g0122 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02004 | hp1 | a0003 | c0017 | t0001 | g0008 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0174 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02055 | hp1 | a0002 | c0004 | t0002 | g0164 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02055 | hp2 | a0002 | c0004 | t0002 | g0002 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02056 | hp1 | a0001 | c0010 | t0002 | g0082 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02074 | hp1 | a0001 | c0003 | t0002 | g0096 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02145 | hp1 | a0002 | c0011 | t0003 | g0210 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02145 | hp2 | a0002 | c0006 | t0001 | g0219 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | CDX | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0264 | EAS | CDX | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02257 | hp1 | a0006 | c0015 | t0004 | g0228 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02258 | hp2 | a0004 | c0013 | t0001 | g0249 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02280 | hp1 | a0001 | c0016 | t0002 | g0201 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0246 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0242 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02572 | hp2 | a0011 | c0029 | t0001 | g0199 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02622 | hp1 | a0004 | c0008 | t0004 | g0170 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02622 | hp2 | a0004 | c0008 | t0001 | g0171 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02630 | hp1 | a0002 | c0006 | t0006 | g0142 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02630 | hp2 | a0004 | c0008 | t0001 | g0161 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02647 | hp1 | a0001 | c0007 | t0001 | g0104 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02647 | hp2 | a0004 | c0027 | t0002 | g0251 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02717 | hp1 | a0002 | c0004 | t0002 | g0227 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02717 | hp2 | a0002 | c0006 | t0001 | g0215 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02723 | hp1 | a0005 | c0009 | t0003 | g0202 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02723 | hp2 | a0002 | c0004 | t0002 | g0002 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02809 | hp1 | a0005 | c0009 | t0003 | g0203 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02809 | hp2 | a0002 | c0006 | t0001 | g0212 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02818 | hp1 | a0007 | c0014 | t0001 | g0252 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02818 | hp2 | a0001 | c0003 | t0005 | g0144 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02886 | hp2 | a0005 | c0009 | t0002 | g0217 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02895 | hp1 | a0002 | c0004 | t0002 | g0012 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02896 | hp1 | a0002 | c0004 | t0002 | g0231 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02896 | hp2 | a0001 | c0007 | t0001 | g0188 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0189 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02922 | hp1 | a0007 | c0014 | t0001 | g0146 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02922 | hp2 | a0002 | c0006 | t0001 | g0156 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02965 | hp1 | a0002 | c0004 | t0002 | g0162 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02965 | hp2 | a0004 | c0008 | t0004 | g0168 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02970 | hp2 | a0001 | c0007 | t0001 | g0198 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02976 | hp1 | a0002 | c0004 | t0002 | g0225 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02976 | hp2 | a0001 | c0007 | t0002 | g0014 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03017 | hp1 | a0001 | c0012 | t0002 | g0001 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03017 | hp2 | a0012 | c0021 | t0002 | g0038 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03041 | hp1 | a0005 | c0009 | t0003 | g0204 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03041 | hp2 | a0001 | c0019 | t0003 | g0205 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03098 | hp1 | a0005 | c0009 | t0002 | g0220 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03139 | hp2 | a0004 | c0030 | t0001 | g0187 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03195 | hp1 | a0002 | c0004 | t0002 | g0224 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0143 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0173 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03225 | hp2 | a0002 | c0006 | t0001 | g0211 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03453 | hp1 | a0001 | c0007 | t0002 | g0118 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03486 | hp1 | a0002 | c0006 | t0001 | g0222 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03486 | hp2 | a0001 | c0007 | t0003 | g0191 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0193 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03540 | hp2 | a0004 | c0013 | t0004 | g0234 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03654 | hp1 | a0008 | c0022 | t0001 | g0071 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0039 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03831 | hp2 | a0003 | c0005 | t0001 | g0133 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0268 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0105 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0165 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18522 | hp2 | a0001 | c0007 | t0003 | g0190 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18906 | hp1 | a0006 | c0015 | t0004 | g0230 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18906 | hp2 | a0002 | c0006 | t0001 | g0213 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18962 | hp1 | a0001 | c0025 | t0002 | g0253 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18967 | hp1 | a0003 | c0005 | t0002 | g0025 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0108 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0270 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19030 | hp1 | a0004 | c0033 | t0001 | g0172 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19030 | hp2 | a0001 | c0020 | t0001 | g0029 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19043 | hp1 | a0001 | c0028 | t0001 | g0275 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19043 | hp2 | a0004 | c0008 | t0004 | g0237 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19070 | hp2 | a0013 | c0024 | t0001 | g0055 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19087 | hp2 | a0001 | c0003 | t0002 | g0115 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19240 | hp1 | a0002 | c0004 | t0002 | g0002 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19240 | hp2 | a0008 | c0034 | t0001 | g0200 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20129 | hp1 | a0001 | c0010 | t0001 | g0028 | AFR | ASW | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20129 | hp2 | a0002 | c0004 | t0002 | g0223 | AFR | ASW | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0076 | SAS | GIH | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0016 | SAS | GIH | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02109 | hp1 | a0002 | c0011 | t0003 | g0209 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02559 | hp1 | a0002 | c0004 | t0002 | g0163 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0192 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03471 | hp1 | a0004 | c0008 | t0004 | g0169 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03471 | hp2 | a0002 | c0006 | t0001 | g0218 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG06807 | hp1 | a0001 | c0003 | t0005 | g0145 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG06807 | hp2 | a0001 | c0007 | t0001 | g0117 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20300 | hp1 | a0001 | c0035 | t0001 | g0157 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0166 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0051 | REF | REF | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0073 | REF | REF | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130188542 | G | A | 1 | a0003 | 13 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(10): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85His | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/19 | 452/3305 | 254/2568 | 85/855 | chr11 | 130188542 | |||
| chr11:130189749 | G | A | 1 | a0010 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.451G>A | p.Val151Ile | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 649/3305 | 451/2568 | 151/855 | chr11 | 130189749 | |||
| chr11:130189752 | A | G | 1 | a0005 | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
missense_variant | MODERATE | c.454A>G | p.Ile152Val | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 652/3305 | 454/2568 | 152/855 | chr11 | 130189752 | |||
| chr11:130190674 | G | A | 1 | a0002 | 29 | HG01099.hp1 HG01496.hp1 HG01891.hp1 others(26): Show |
missense_variant | MODERATE | c.855G>A | p.Met285Ile | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 1053/3305 | 855/2568 | 285/855 | chr11 | 130190674 | |||
| chr11:130194204 | G | A | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.931G>A | p.Val311Ile | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/19 | 1129/3305 | 931/2568 | 311/855 | chr11 | 130194204 | |||
| chr11:130194658 | G | A | 1 | a0012 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1034G>A | p.Arg345His | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/19 | 1232/3305 | 1034/2568 | 345/855 | chr11 | 130194658 | |||
| chr11:130194672 | A | G | 1 | a0004 | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
missense_variant | MODERATE | c.1048A>G | p.Thr350Ala | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/19 | 1246/3305 | 1048/2568 | 350/855 | chr11 | 130194672 | |||
| chr11:130196366 | C | A | 2 | a0006 a0008 |
4 | HG02257.hp1 HG03654.hp1 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.1141C>A | p.Arg381Ser | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/19 | 1339/3305 | 1141/2568 | 381/855 | chr11 | 130196366 | |||
| chr11:130198991 | G | A | 1 | a0006 | 2 | HG02257.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1729G>A | p.Gly577Arg | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/19 | 1927/3305 | 1729/2568 | 577/855 | chr11 | 130198991 | |||
| chr11:130199999 | C | T | 1 | a0013 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.1856C>T | p.Thr619Met | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/19 | 2054/3305 | 1856/2568 | 619/855 | chr11 | 130199999 | |||
| chr11:130208579 | G | C | 1 | a0009 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2164G>C | p.Glu722Gln | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/19 | 2362/3305 | 2164/2568 | 722/855 | chr11 | 130208579 | |||
| chr11:130209529 | C | T | 1 | a0007 | 2 | HG02818.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.2357C>T | p.Pro786Leu | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 18/19 | 2555/3305 | 2357/2568 | 786/855 | chr11 | 130209529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130160000 | C | T | 1 | a0001c0035 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.21C>T | p.Arg7Arg | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/19 | 219/3305 | 21/2568 | 7/855 | chr11 | 130160000 | |||
| chr11:130188152 | A | G | 12 | a0001c0007 a0001c0016 a0001c0031 others(9): Show |
34 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(31): Show |
synonymous_variant | LOW | c.120A>G | p.Pro40Pro | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/19 | 318/3305 | 120/2568 | 40/855 | chr11 | 130188152 | |||
| chr11:130188603 | C | T | 1 | a0008c0034 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.315C>T | p.Tyr105Tyr | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/19 | 513/3305 | 315/2568 | 105/855 | chr11 | 130188603 | |||
| chr11:130189823 | G | A | 1 | a0001c0019 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.525G>A | p.Glu175Glu | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 723/3305 | 525/2568 | 175/855 | chr11 | 130189823 | |||
| chr11:130189853 | G | A | 1 | a0001c0020 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.555G>A | p.Ala185Ala | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 753/3305 | 555/2568 | 185/855 | chr11 | 130189853 | |||
| chr11:130190482 | C | T | 1 | a0001c0028 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.663C>T | p.Arg221Arg | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 861/3305 | 663/2568 | 221/855 | chr11 | 130190482 | |||
| chr11:130190617 | G | A | 3 | a0004c0030 a0007c0014 a0011c0029 |
4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.798G>A | p.Ala266Ala | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 996/3305 | 798/2568 | 266/855 | chr11 | 130190617 | |||
| chr11:130190659 | C | T | 1 | a0004c0030 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.840C>T | p.Asn280Asn | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 1038/3305 | 840/2568 | 280/855 | chr11 | 130190659 | |||
| chr11:130196440 | C | T | 18 | a0001c0001 a0001c0010 a0001c0012 others(15): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
synonymous_variant | LOW | c.1215C>T | p.Asn405Asn | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/19 | 1413/3305 | 1215/2568 | 405/855 | chr11 | 130196440 | |||
| chr11:130196606 | C | T | 5 | a0004c0008 a0004c0013 a0004c0027 others(2): Show |
12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
synonymous_variant | LOW | c.1260C>T | p.Ser420Ser | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/19 | 1458/3305 | 1260/2568 | 420/855 | chr11 | 130196606 | |||
| chr11:130197869 | G | T | 1 | a0001c0026 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1383G>T | p.Thr461Thr | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/19 | 1581/3305 | 1383/2568 | 461/855 | chr11 | 130197869 | |||
| chr11:130198312 | C | T | 1 | a0001c0025 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.1464C>T | p.Cys488Cys | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/19 | 1662/3305 | 1464/2568 | 488/855 | chr11 | 130198312 | |||
| chr11:130198390 | C | T | 3 | a0004c0008 a0004c0013 a0004c0030 |
10 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.1542C>T | p.Cys514Cys | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/19 | 1740/3305 | 1542/2568 | 514/855 | chr11 | 130198390 | |||
| chr11:130198596 | G | C | 5 | a0001c0002 a0001c0010 a0001c0020 others(2): Show |
47 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(44): Show |
synonymous_variant | LOW | c.1659G>C | p.Gly553Gly | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/19 | 1857/3305 | 1659/2568 | 553/855 | chr11 | 130198596 | |||
| chr11:130199026 | C | T | 1 | a0003c0017 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.1764C>T | p.Asp588Asp | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/19 | 1962/3305 | 1764/2568 | 588/855 | chr11 | 130199026 | |||
| chr11:130209679 | C | T | 1 | a0001c0012 | 2 | HG01257.hp2 HG03017.hp1 |
synonymous_variant | LOW | c.2424C>T | p.Pro808Pro | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 2622/3305 | 2424/2568 | 808/855 | chr11 | 130209679 | |||
| chr11:130209688 | C | T | 1 | a0001c0023 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.2433C>T | p.Ser811Ser | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 2631/3305 | 2433/2568 | 811/855 | chr11 | 130209688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130159881 | T | C | 2 | a0001c0003t0005 a0002c0006t0006 |
4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-99T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/19 | 99 | chr11 | 130159881 | ||||||
| chr11:130210024 | G | C | 1 | a0001c0031t0007 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*201G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 201 | chr11 | 130210024 | ||||||
| chr11:130210088 | C | G | 1 | a0001c0001t0008 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 265 | chr11 | 130210088 | ||||||
| chr11:130210122 | C | T | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*299C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 299 | chr11 | 130210122 | ||||||
| chr11:130210142 | C | G | 17 | a0001c0001t0002 a0001c0001t0008 a0001c0002t0002 others(14): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 319 | chr11 | 130210142 | ||||||
| chr11:130210170 | G | A | 17 | a0001c0001t0002 a0001c0001t0008 a0001c0002t0002 others(14): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*347G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 347 | chr11 | 130210170 | ||||||
| chr11:130210313 | C | T | 4 | a0001c0001t0004 a0004c0008t0004 a0004c0013t0004 others(1): Show |
10 | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*490C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 490 | chr11 | 130210313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130160143 | C | T | 30 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(27): Show |
31 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.81+83C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160143 | |||||||
| chr11:130160198 | C | G | 2 | a0001c0001t0001g0248 a0001c0001t0002g0247 |
2 | NA18979.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.81+138C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160198 | |||||||
| chr11:130160468 | C | G | 118 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0265 others(115): Show |
122 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.81+408C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160468 | |||||||
| chr11:130160487 | T | A | 1 | a0004c0008t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.81+427T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160487 | |||||||
| chr11:130160668 | A | T | 1 | a0001c0001t0002g0160 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.81+608A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160668 | |||||||
| chr11:130160677 | G | C | 1 | a0004c0013t0001g0249 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+617G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160677 | |||||||
| chr11:130160876 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.81+816A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160876 | |||||||
| chr11:130161044 | C | G | 1 | a0001c0001t0002g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.81+984C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161044 | |||||||
| chr11:130161391 | AC | A | 37 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(34): Show |
38 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.81+1333delC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130161391 | ||||||
| chr11:130161565 | T | A | 14 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(11): Show |
15 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+1505T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161565 | |||||||
| chr11:130161584 | AC | A | 15 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0250 others(12): Show |
15 | HG00140.hp2 HG00673.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+1529delC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130161584 | ||||||
| chr11:130161740 | G | A | 1 | a0001c0007t0002g0014 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+1680G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161740 | |||||||
| chr11:130161934 | A | G | 137 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0147 others(134): Show |
143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.81+1874A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161934 | |||||||
| chr11:130161970 | C | G | 4 | a0001c0001t0001g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(1): Show |
4 | HG02615.hp1 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1910C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161970 | |||||||
| chr11:130162195 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.81+2135A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162195 | |||||||
| chr11:130162250 | G | A | 1 | a0004c0030t0001g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.81+2190G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162250 | |||||||
| chr11:130162590 | T | C | 4 | a0001c0007t0001g0188 a0001c0007t0001g0189 a0001c0007t0003g0190 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2530T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162590 | |||||||
| chr11:130162628 | A | G | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+2568A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162628 | |||||||
| chr11:130162771 | C | G | 3 | a0001c0001t0002g0134 a0001c0012t0002g0136 a0001c0026t0002g0135 |
3 | HG01099.hp2 HG01257.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+2711C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162771 | |||||||
| chr11:130162773 | A | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2713A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162773 | |||||||
| chr11:130162822 | C | G | 1 | a0003c0005t0001g0133 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+2762C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162822 | |||||||
| chr11:130162940 | T | C | 77 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0147 others(74): Show |
80 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.81+2880T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162940 | |||||||
| chr11:130163121 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81+3061C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163121 | |||||||
| chr11:130163122 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.81+3062G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163122 | |||||||
| chr11:130163675 | G | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+3615G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163675 | |||||||
| chr11:130163722 | C | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+3662C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163722 | |||||||
| chr11:130163785 | G | A | 4 | a0002c0004t0002g0012 a0002c0004t0002g0162 a0002c0004t0002g0163 others(1): Show |
5 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+3725G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163785 | |||||||
| chr11:130163975 | A | G | 36 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(33): Show |
37 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.81+3915A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163975 | |||||||
| chr11:130164021 | C | G | 1 | a0001c0023t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+3961C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164021 | |||||||
| chr11:130164082 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+4022C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164082 | |||||||
| chr11:130164252 | G | A | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+4192G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164252 | |||||||
| chr11:130164281 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0147 others(1): Show |
6 | HG00408.hp1 NA18969.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+4221T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164281 | |||||||
| chr11:130164284 | T | C | 1 | a0002c0004t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+4224T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164284 | |||||||
| chr11:130164427 | T | C | 1 | a0001c0003t0001g0016 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+4367T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164427 | |||||||
| chr11:130164529 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+4469C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164529 | |||||||
| chr11:130164636 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+4576C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164636 | |||||||
| chr11:130164683 | T | C | 136 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.81+4623T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164683 | |||||||
| chr11:130164718 | C | CTTA | 25 | a0001c0001t0001g0276 a0001c0001t0002g0023 a0001c0001t0002g0024 others(22): Show |
26 | HG01243.hp1 HG01261.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.81+4691_81+4693dup others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | C | CTTATTA | 19 | a0001c0001t0001g0019 a0001c0001t0002g0018 a0001c0001t0004g0196 others(16): Show |
19 | HG00597.hp2 HG00673.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+4688_81+4693dup others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | C | CTTATTAT others(2): Show |
36 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0002g0179 others(33): Show |
36 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+4685_81+4693dup others(9): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | C | CTTATTAT others(5): Show |
29 | a0001c0001t0002g0256 a0001c0001t0003g0243 a0001c0002t0001g0165 others(26): Show |
29 | HG00423.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.81+4682_81+4693dup others(12): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | C | CTTATTAT others(8): Show |
3 | a0001c0001t0001g0233 a0004c0027t0002g0251 a0008c0034t0001g0200 |
3 | HG02109.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.81+4679_81+4693dup others(15): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | CTTA | C | 4 | a0002c0004t0002g0012 a0002c0004t0002g0162 a0002c0004t0002g0163 others(1): Show |
5 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+4691_81+4693del others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | CTTATTA | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0147 a0001c0001t0001g0229 others(9): Show |
15 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+4688_81+4693del others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164718 | CTTATTAT others(2): Show |
C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0130 others(8): Show |
13 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+4685_81+4693del others(9): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | ||||||
| chr11:130164794 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+4734A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164794 | |||||||
| chr11:130164841 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.81+4781G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164841 | |||||||
| chr11:130164844 | T | A | 1 | a0001c0028t0001g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+4784T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164844 | |||||||
| chr11:130164894 | T | A | 18 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(15): Show |
19 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+4834T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164894 | |||||||
| chr11:130164989 | G | A | 1 | a0003c0005t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.81+4929G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164989 | |||||||
| chr11:130165000 | G | A | 13 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(10): Show |
14 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+4940G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165000 | |||||||
| chr11:130165110 | C | T | 1 | a0004c0033t0001g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+5050C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165110 | |||||||
| chr11:130165190 | C | T | 64 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(61): Show |
65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.81+5130C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165190 | |||||||
| chr11:130165204 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.81+5144C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165204 | |||||||
| chr11:130165290 | T | A | 136 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.81+5230T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165290 | |||||||
| chr11:130165387 | G | A | 2 | a0001c0002t0001g0165 a0001c0003t0001g0166 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.81+5327G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165387 | |||||||
| chr11:130165410 | G | A | 2 | a0001c0001t0001g0155 a0001c0010t0001g0028 |
2 | HG01069.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.81+5350G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165410 | |||||||
| chr11:130165560 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.81+5500T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165560 | |||||||
| chr11:130165703 | C | T | 63 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(60): Show |
64 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.81+5643C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165703 | |||||||
| chr11:130166099 | G | A | 1 | a0001c0020t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81+6039G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166099 | |||||||
| chr11:130166310 | T | A | 1 | a0001c0002t0001g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+6250T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166310 | |||||||
| chr11:130166476 | C | T | 1 | a0001c0003t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+6416C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166476 | |||||||
| chr11:130166749 | T | C | 23 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(20): Show |
24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+6689T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166749 | |||||||
| chr11:130166791 | G | A | 1 | a0001c0031t0007g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.81+6731G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166791 | |||||||
| chr11:130166932 | C | T | 1 | a0001c0003t0005g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81+6872C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166932 | |||||||
| chr11:130166939 | G | A | 1 | a0001c0002t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+6879G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166939 | |||||||
| chr11:130166963 | C | T | 17 | a0001c0001t0001g0127 a0001c0001t0002g0128 a0001c0001t0002g0179 others(14): Show |
17 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+6903C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166963 | |||||||
| chr11:130166982 | C | T | 1 | a0001c0002t0001g0274 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.81+6922C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166982 | |||||||
| chr11:130167121 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+7061G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167121 | |||||||
| chr11:130167212 | A | G | 20 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0003t0001g0216 others(17): Show |
20 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+7152A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167212 | |||||||
| chr11:130167218 | A | T | 1 | a0004c0033t0001g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+7158A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167218 | |||||||
| chr11:130167273 | G | C | 1 | a0001c0001t0002g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.81+7213G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167273 | |||||||
| chr11:130167301 | A | T | 13 | a0001c0001t0001g0120 a0003c0005t0001g0008 a0003c0005t0001g0027 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+7241A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167301 | |||||||
| chr11:130167427 | T | A | 1 | a0001c0003t0001g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+7367T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167427 | |||||||
| chr11:130167767 | T | G | 1 | a0001c0001t0002g0250 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.81+7707T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167767 | |||||||
| chr11:130167778 | G | A | 3 | a0001c0003t0001g0206 a0001c0019t0003g0205 a0001c0023t0001g0232 |
3 | HG01074.hp2 HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+7718G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167778 | |||||||
| chr11:130167807 | C | T | 2 | a0001c0001t0001g0155 a0001c0010t0001g0028 |
2 | HG01069.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.81+7747C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167807 | |||||||
| chr11:130168008 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.81+7948C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168008 | |||||||
| chr11:130168010 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.81+7950C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168010 | |||||||
| chr11:130168081 | G | C | 139 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
146 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.81+8021G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168081 | |||||||
| chr11:130168132 | A | G | 23 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(20): Show |
24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+8072A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168132 | |||||||
| chr11:130168479 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.81+8419G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168479 | |||||||
| chr11:130168592 | A | C | 120 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.81+8532A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168592 | |||||||
| chr11:130168829 | C | A | 4 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0002c0011t0003g0209 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+8769C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168829 | |||||||
| chr11:130168960 | T | C | 1 | a0001c0002t0002g0244 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+8900T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168960 | |||||||
| chr11:130169034 | TA | T | 119 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(116): Show |
125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.81+8983delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169034 | ||||||
| chr11:130169063 | C | T | 23 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(20): Show |
24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+9003C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169063 | |||||||
| chr11:130169075 | T | C | 1 | a0001c0002t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+9015T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169075 | |||||||
| chr11:130169091 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.81+9031G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169091 | |||||||
| chr11:130169092 | G | GT | 28 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0109 others(25): Show |
28 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.81+9054dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | ||||||
| chr11:130169092 | G | GTT | 18 | a0001c0001t0001g0114 a0001c0003t0001g0167 a0001c0003t0002g0115 others(15): Show |
19 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+9053_81+9054dup others(2): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | ||||||
| chr11:130169092 | G | GTTT | 6 | a0001c0003t0005g0143 a0001c0003t0005g0144 a0001c0003t0005g0145 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+9052_81+9054dup others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | ||||||
| chr11:130169092 | GT | G | 37 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0272 others(34): Show |
39 | HG00621.hp2 HG01243.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.81+9054delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | ||||||
| chr11:130169092 | GTT | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.81+9053_81+9054del others(2): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | ||||||
| chr11:130169092 | GTTT | G | 11 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0002t0001g0207 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+9052_81+9054del others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | ||||||
| chr11:130169153 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81+9093G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169153 | |||||||
| chr11:130169382 | A | C | 2 | a0001c0001t0001g0093 a0001c0001t0002g0092 |
2 | NA18959.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.81+9322A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169382 | |||||||
| chr11:130169518 | C | T | 20 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0003t0001g0216 others(17): Show |
20 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+9458C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169518 | |||||||
| chr11:130169605 | G | A | 14 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(11): Show |
15 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+9545G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169605 | |||||||
| chr11:130169698 | G | A | 1 | a0012c0021t0002g0038 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+9638G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169698 | |||||||
| chr11:130170231 | C | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0086 a0013c0024t0001g0055 |
3 | NA18940.hp2 NA18990.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.81+10171C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170231 | |||||||
| chr11:130170331 | G | T | 1 | a0001c0001t0002g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.81+10271G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170331 | |||||||
| chr11:130170610 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0002g0092 |
2 | NA18959.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.81+10550G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170610 | |||||||
| chr11:130170644 | GGGTTCCT others(23): Show |
G | 1 | a0002c0004t0002g0223 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+10595_81+10624d others(32): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130170644 | ||||||
| chr11:130170718 | C | T | 1 | a0005c0009t0003g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.81+10658C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170718 | |||||||
| chr11:130170758 | G | C | 1 | a0002c0004t0002g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.81+10698G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170758 | |||||||
| chr11:130171049 | A | G | 23 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(20): Show |
24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+10989A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171049 | |||||||
| chr11:130171268 | C | T | 1 | a0001c0002t0001g0152 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.81+11208C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171268 | |||||||
| chr11:130171311 | T | C | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+11251T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171311 | |||||||
| chr11:130171339 | C | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
36 | HG00408.hp1 HG00438.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+11279C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171339 | |||||||
| chr11:130171362 | C | A | 2 | a0004c0013t0001g0249 a0004c0027t0002g0251 |
2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.81+11302C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171362 | |||||||
| chr11:130171555 | G | A | 1 | a0001c0035t0001g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+11495G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171555 | |||||||
| chr11:130171586 | G | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
36 | HG00408.hp1 HG00438.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+11526G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171586 | |||||||
| chr11:130171652 | T | C | 1 | a0001c0023t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+11592T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171652 | |||||||
| chr11:130171660 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.81+11600A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171660 | |||||||
| chr11:130171760 | C | A | 2 | a0004c0008t0001g0161 a0004c0008t0001g0171 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.81+11700C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171760 | |||||||
| chr11:130171961 | G | A | 15 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0002g0236 others(12): Show |
17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+11901G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171961 | |||||||
| chr11:130172145 | C | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(128): Show |
136 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.81+12085C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172145 | |||||||
| chr11:130172170 | A | T | 1 | a0001c0001t0002g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.81+12110A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172170 | |||||||
| chr11:130172216 | G | A | 1 | a0001c0003t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.81+12156G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172216 | |||||||
| chr11:130172274 | T | A | 5 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02040.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+12214T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172274 | |||||||
| chr11:130172275 | A | T | 2 | a0001c0001t0002g0089 a0001c0001t0002g0113 |
2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.81+12215A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172275 | |||||||
| chr11:130172411 | C | CT | 22 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0109 others(19): Show |
22 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+12375dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130172411 | ||||||
| chr11:130172411 | CT | C | 69 | a0001c0001t0001g0042 a0001c0001t0001g0127 a0001c0001t0001g0265 others(66): Show |
72 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.81+12375delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130172411 | ||||||
| chr11:130172486 | C | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+12426C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172486 | |||||||
| chr11:130172487 | G | C | 1 | a0001c0002t0001g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.81+12427G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172487 | |||||||
| chr11:130172518 | C | T | 1 | a0002c0006t0001g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.81+12458C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172518 | |||||||
| chr11:130172527 | C | T | 23 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(20): Show |
24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+12467C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172527 | |||||||
| chr11:130172568 | C | T | 3 | a0001c0003t0002g0107 a0001c0003t0002g0108 a0001c0003t0002g0116 |
3 | NA18982.hp1 NA19000.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.81+12508C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172568 | |||||||
| chr11:130172707 | G | A | 1 | a0012c0021t0002g0038 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+12647G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172707 | |||||||
| chr11:130172915 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.81+12855G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172915 | |||||||
| chr11:130172964 | G | A | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.81+12904G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172964 | |||||||
| chr11:130172964 | G | T | 34 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(31): Show |
35 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.81+12904G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172964 | |||||||
| chr11:130173058 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.81+12998G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173058 | |||||||
| chr11:130173360 | G | A | 1 | a0004c0013t0004g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+13300G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173360 | |||||||
| chr11:130173431 | G | A | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
66 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.81+13371G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173431 | |||||||
| chr11:130173572 | C | T | 3 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
3 | NA18941.hp1 NA18962.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.81+13512C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173572 | |||||||
| chr11:130173595 | C | CA | 21 | a0001c0001t0001g0109 a0001c0001t0001g0137 a0001c0001t0001g0229 others(18): Show |
23 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.81+13551dupA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130173595 | ||||||
| chr11:130173595 | CA | C | 28 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(25): Show |
29 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.81+13551delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130173595 | ||||||
| chr11:130173685 | G | A | 34 | a0001c0001t0001g0127 a0001c0001t0002g0033 a0001c0001t0002g0128 others(31): Show |
34 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.81+13625G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173685 | |||||||
| chr11:130173894 | C | G | 1 | a0001c0001t0002g0024 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.81+13834C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173894 | |||||||
| chr11:130174020 | G | C | 1 | a0002c0004t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+13960G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174020 | |||||||
| chr11:130174083 | A | G | 12 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(9): Show |
12 | HG01074.hp2 HG01261.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+14023A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174083 | |||||||
| chr11:130174336 | A | T | 35 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(32): Show |
36 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.82-13778A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174336 | |||||||
| chr11:130174340 | G | T | 23 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(20): Show |
24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-13774G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174340 | |||||||
| chr11:130174520 | G | T | 35 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(32): Show |
36 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.82-13594G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174520 | |||||||
| chr11:130174592 | A | G | 4 | a0001c0003t0005g0143 a0001c0003t0005g0144 a0001c0003t0005g0145 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-13522A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174592 | |||||||
| chr11:130174614 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.82-13500T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174614 | |||||||
| chr11:130174988 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-13126G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174988 | |||||||
| chr11:130175138 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-12976C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175138 | |||||||
| chr11:130175139 | G | A | 1 | a0007c0014t0001g0146 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.82-12975G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175139 | |||||||
| chr11:130175205 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.82-12909G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175205 | |||||||
| chr11:130175219 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-12895T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175219 | |||||||
| chr11:130175303 | G | GT | 9 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0002g0256 others(6): Show |
9 | HG01123.hp1 HG01496.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-12802dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130175303 | ||||||
| chr11:130175303 | G | T | 1 | a0001c0020t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-12811G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175303 | |||||||
| chr11:130175304 | T | G | 2 | a0001c0002t0001g0165 a0001c0003t0001g0166 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.82-12810T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175304 | |||||||
| chr11:130175440 | C | T | 4 | a0005c0009t0003g0202 a0005c0009t0003g0203 a0005c0009t0003g0204 others(1): Show |
4 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-12674C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175440 | |||||||
| chr11:130175540 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-12574C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175540 | |||||||
| chr11:130175601 | A | G | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.82-12513A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175601 | |||||||
| chr11:130175871 | C | A | 1 | a0001c0001t0002g0271 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.82-12243C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175871 | |||||||
| chr11:130175897 | A | G | 2 | a0001c0003t0001g0216 a0002c0006t0001g0222 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.82-12217A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175897 | |||||||
| chr11:130175912 | C | T | 1 | a0002c0006t0001g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.82-12202C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175912 | |||||||
| chr11:130176033 | G | A | 1 | a0004c0008t0004g0169 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82-12081G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176033 | |||||||
| chr11:130176044 | C | T | 13 | a0001c0002t0001g0165 a0001c0003t0001g0166 a0001c0003t0001g0167 others(10): Show |
14 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-12070C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176044 | |||||||
| chr11:130176083 | G | C | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.82-12031G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176083 | |||||||
| chr11:130176247 | T | C | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.82-11867T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176247 | |||||||
| chr11:130176328 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.82-11786G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176328 | |||||||
| chr11:130176370 | CT | C | 8 | a0001c0001t0001g0153 a0001c0001t0002g0036 a0001c0001t0002g0141 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-11732delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176370 | ||||||
| chr11:130176493 | G | A | 69 | a0001c0001t0001g0127 a0001c0001t0001g0265 a0001c0001t0001g0272 others(66): Show |
70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.82-11621G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176493 | |||||||
| chr11:130176683 | C | T | 3 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0033t0001g0172 |
3 | HG02622.hp2 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.82-11431C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176683 | |||||||
| chr11:130176788 | C | CT | 25 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0109 others(22): Show |
25 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-11298dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | ||||||
| chr11:130176788 | CT | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0091 others(50): Show |
56 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.82-11298delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | ||||||
| chr11:130176788 | CTT | C | 40 | a0001c0001t0001g0130 a0001c0001t0001g0265 a0001c0001t0001g0272 others(37): Show |
41 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.82-11299_82-11298d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | ||||||
| chr11:130176788 | CTTT | C | 16 | a0001c0003t0001g0166 a0001c0003t0001g0167 a0001c0003t0001g0246 others(13): Show |
17 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.82-11300_82-11298d others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | ||||||
| chr11:130176788 | CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0001g0229 a0001c0003t0001g0216 a0002c0004t0002g0002 others(7): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-11308_82-11298d others(13): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | ||||||
| chr11:130176788 | CTTTTTTT others(5): Show |
C | 1 | a0002c0004t0002g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.82-11309_82-11298d others(14): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | ||||||
| chr11:130176821 | C | T | 1 | a0001c0002t0001g0022 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-11293C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176821 | |||||||
| chr11:130176954 | G | A | 1 | a0002c0004t0002g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.82-11160G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176954 | |||||||
| chr11:130177014 | G | C | 34 | a0001c0001t0001g0127 a0001c0001t0002g0033 a0001c0001t0002g0128 others(31): Show |
34 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.82-11100G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177014 | |||||||
| chr11:130177033 | C | T | 1 | a0001c0002t0002g0257 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.82-11081C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177033 | |||||||
| chr11:130177097 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0002t0001g0207 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-11017G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177097 | |||||||
| chr11:130177254 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.82-10860C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177254 | |||||||
| chr11:130177569 | C | A | 116 | a0001c0001t0001g0127 a0001c0001t0001g0233 a0001c0001t0001g0265 others(113): Show |
118 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.82-10545C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177569 | |||||||
| chr11:130177779 | GAA | G | 3 | a0002c0004t0002g0012 a0002c0004t0002g0163 a0002c0004t0002g0164 |
4 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-10334_82-10333d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177779 | |||||||
| chr11:130177910 | G | C | 5 | a0001c0007t0001g0188 a0001c0007t0001g0189 a0001c0007t0003g0190 others(2): Show |
5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-10204G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177910 | |||||||
| chr11:130178050 | T | C | 1 | a0008c0034t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82-10064T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178050 | |||||||
| chr11:130178091 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.82-10023A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178091 | |||||||
| chr11:130178125 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.82-9989T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178125 | |||||||
| chr11:130178151 | C | T | 1 | a0002c0004t0001g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.82-9963C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178151 | |||||||
| chr11:130178392 | T | TTATGGCC others(121): Show |
104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.82-9720_82-9719ins others(128): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130178392 | ||||||
| chr11:130178392 | T | TTATGGCC others(121): Show |
37 | a0001c0001t0001g0127 a0001c0001t0002g0033 a0001c0001t0002g0128 others(34): Show |
37 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.82-9720_82-9719ins others(128): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130178392 | ||||||
| chr11:130178506 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.82-9608C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178506 | |||||||
| chr11:130178530 | G | T | 1 | a0001c0028t0001g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-9584G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178530 | |||||||
| chr11:130178871 | G | T | 14 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0003t0001g0216 others(11): Show |
14 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-9243G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178871 | |||||||
| chr11:130178962 | C | G | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82-9152C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178962 | |||||||
| chr11:130178979 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.82-9135C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178979 | |||||||
| chr11:130179931 | G | A | 1 | a0001c0003t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.82-8183G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130179931 | |||||||
| chr11:130180000 | G | C | 1 | a0001c0002t0001g0050 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.82-8114G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180000 | |||||||
| chr11:130180000 | G | T | 1 | a0002c0006t0001g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-8114G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180000 | |||||||
| chr11:130180048 | G | T | 1 | a0001c0002t0001g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.82-8066G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180048 | |||||||
| chr11:130180097 | C | T | 1 | a0001c0003t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-8017C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180097 | |||||||
| chr11:130180155 | C | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-7959C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180155 | |||||||
| chr11:130180483 | G | C | 1 | a0003c0005t0001g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.82-7631G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180483 | |||||||
| chr11:130180593 | G | A | 1 | a0002c0006t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.82-7521G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180593 | |||||||
| chr11:130180845 | G | A | 1 | a0001c0023t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.82-7269G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180845 | |||||||
| chr11:130180927 | G | A | 127 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0026 others(124): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.82-7187G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180927 | |||||||
| chr11:130180988 | C | A | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-7126C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180988 | |||||||
| chr11:130181117 | TGTCCCTG others(18): Show |
T | 2 | a0004c0008t0004g0237 a0004c0008t0004g0238 |
2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82-6976_82-6952del others(25): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130181117 | ||||||
| chr11:130181210 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.82-6904G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181210 | |||||||
| chr11:130181245 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.82-6869G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181245 | |||||||
| chr11:130181261 | G | A | 1 | a0001c0003t0001g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.82-6853G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181261 | |||||||
| chr11:130181270 | C | T | 29 | a0001c0001t0001g0127 a0001c0001t0002g0033 a0001c0001t0002g0179 others(26): Show |
29 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.82-6844C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181270 | |||||||
| chr11:130181285 | C | T | 4 | a0001c0003t0005g0143 a0001c0003t0005g0144 a0001c0003t0005g0145 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-6829C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181285 | |||||||
| chr11:130181365 | G | A | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-6749G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181365 | |||||||
| chr11:130181455 | C | T | 1 | a0008c0034t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82-6659C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181455 | |||||||
| chr11:130181652 | C | T | 34 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(31): Show |
35 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.82-6462C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181652 | |||||||
| chr11:130181772 | T | C | 2 | a0002c0004t0001g0192 a0011c0029t0001g0199 |
2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.82-6342T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181772 | |||||||
| chr11:130181773 | G | A | 2 | a0001c0001t0002g0031 a0008c0022t0001g0071 |
2 | HG01516.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.82-6341G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181773 | |||||||
| chr11:130182004 | C | T | 29 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(26): Show |
30 | HG00621.hp2 HG00642.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-6110C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182004 | |||||||
| chr11:130182057 | A | G | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-6057A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182057 | |||||||
| chr11:130182114 | A | G | 244 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.82-6000A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182114 | |||||||
| chr11:130182309 | G | GT | 3 | a0001c0003t0005g0143 a0001c0003t0005g0144 a0001c0003t0005g0145 |
3 | HG02818.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82-5802dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130182309 | ||||||
| chr11:130182360 | C | T | 1 | a0001c0001t0002g0266 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.82-5754C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182360 | |||||||
| chr11:130182361 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.82-5753G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182361 | |||||||
| chr11:130182385 | G | C | 25 | a0001c0001t0001g0229 a0001c0002t0001g0207 a0001c0002t0001g0208 others(22): Show |
27 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-5729G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182385 | |||||||
| chr11:130182417 | G | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
45 | HG00408.hp1 HG00438.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.82-5697G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182417 | |||||||
| chr11:130182448 | G | A | 1 | a0001c0016t0002g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.82-5666G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182448 | |||||||
| chr11:130182514 | T | C | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(243): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.82-5600T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182514 | |||||||
| chr11:130182528 | C | T | 25 | a0001c0001t0001g0229 a0001c0002t0001g0207 a0001c0002t0001g0208 others(22): Show |
27 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-5586C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182528 | |||||||
| chr11:130182566 | C | T | 1 | a0011c0029t0001g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82-5548C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182566 | |||||||
| chr11:130182567 | G | A | 4 | a0001c0003t0005g0143 a0001c0003t0005g0144 a0001c0003t0005g0145 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-5547G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182567 | |||||||
| chr11:130182652 | C | CT | 36 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0276 others(33): Show |
37 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.82-5447dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130182652 | ||||||
| chr11:130182701 | G | A | 3 | a0001c0003t0001g0216 a0002c0006t0001g0156 a0002c0006t0001g0226 |
3 | HG01891.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.82-5413G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182701 | |||||||
| chr11:130182731 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.82-5383T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182731 | |||||||
| chr11:130182731 | T | G | 1 | a0001c0003t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-5383T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182731 | |||||||
| chr11:130182733 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.82-5381T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182733 | |||||||
| chr11:130182750 | A | G | 4 | a0001c0003t0001g0195 a0001c0016t0002g0106 a0001c0031t0007g0030 others(1): Show |
4 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-5364A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182750 | |||||||
| chr11:130182825 | G | A | 183 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(180): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.82-5289G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182825 | |||||||
| chr11:130182849 | C | G | 1 | a0001c0001t0002g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.82-5265C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182849 | |||||||
| chr11:130182908 | C | T | 2 | a0007c0014t0001g0146 a0007c0014t0001g0252 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.82-5206C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182908 | |||||||
| chr11:130182941 | C | T | 2 | a0001c0023t0001g0232 a0001c0035t0001g0157 |
2 | HG01074.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.82-5173C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182941 | |||||||
| chr11:130183017 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.82-5097C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183017 | |||||||
| chr11:130183131 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.82-4983T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183131 | |||||||
| chr11:130183392 | G | A | 29 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0003t0001g0167 others(26): Show |
32 | HG01099.hp1 HG01496.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-4722G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183392 | |||||||
| chr11:130183476 | T | C | 263 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(260): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.82-4638T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183476 | |||||||
| chr11:130183542 | TA | T | 62 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0095 others(59): Show |
65 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.82-4553delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130183542 | ||||||
| chr11:130183673 | C | T | 29 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0003t0001g0167 others(26): Show |
32 | HG01099.hp1 HG01496.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-4441C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183673 | |||||||
| chr11:130183687 | A | T | 1 | a0001c0019t0003g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-4427A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183687 | |||||||
| chr11:130183744 | T | A | 9 | a0001c0007t0001g0104 a0001c0007t0001g0117 a0001c0007t0001g0198 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-4370T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183744 | |||||||
| chr11:130183824 | C | T | 1 | a0001c0003t0001g0195 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.82-4290C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183824 | |||||||
| chr11:130184148 | A | G | 12 | a0001c0007t0001g0104 a0001c0007t0001g0117 a0001c0007t0001g0198 others(9): Show |
12 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-3966A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184148 | |||||||
| chr11:130184169 | C | A | 4 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-3945C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184169 | |||||||
| chr11:130184495 | G | A | 30 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0002g0256 others(27): Show |
31 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.82-3619G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184495 | |||||||
| chr11:130184530 | C | G | 1 | a0001c0001t0002g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-3584C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184530 | |||||||
| chr11:130184565 | T | C | 8 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-3549T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184565 | |||||||
| chr11:130184737 | T | C | 1 | a0001c0003t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-3377T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184737 | |||||||
| chr11:130184873 | G | A | 1 | a0001c0002t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.82-3241G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184873 | |||||||
| chr11:130184882 | A | G | 2 | a0001c0001t0001g0229 a0002c0004t0001g0193 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.82-3232A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184882 | |||||||
| chr11:130184938 | A | G | 12 | a0001c0007t0001g0104 a0001c0007t0001g0117 a0001c0007t0001g0198 others(9): Show |
12 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-3176A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184938 | |||||||
| chr11:130184986 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82-3128C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184986 | |||||||
| chr11:130184987 | C | T | 3 | a0001c0001t0002g0132 a0003c0005t0001g0125 a0003c0005t0001g0133 |
3 | HG00323.hp1 HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.82-3127C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184987 | |||||||
| chr11:130185081 | C | G | 1 | a0001c0019t0003g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-3033C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185081 | |||||||
| chr11:130185221 | A | C | 33 | a0001c0007t0001g0104 a0001c0007t0001g0117 a0001c0007t0001g0188 others(30): Show |
33 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-2893A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185221 | |||||||
| chr11:130185323 | G | A | 1 | a0007c0014t0001g0252 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-2791G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185323 | |||||||
| chr11:130185525 | G | A | 4 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-2589G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185525 | |||||||
| chr11:130185528 | C | A | 1 | a0001c0001t0002g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-2586C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185528 | |||||||
| chr11:130185671 | C | T | 8 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-2443C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185671 | |||||||
| chr11:130185713 | T | C | 108 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0265 others(105): Show |
112 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.82-2401T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185713 | |||||||
| chr11:130185730 | G | T | 6 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0003t0003g0242 others(3): Show |
6 | HG02257.hp2 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-2384G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185730 | |||||||
| chr11:130185868 | C | T | 151 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.82-2246C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185868 | |||||||
| chr11:130185911 | G | A | 4 | a0005c0009t0003g0202 a0005c0009t0003g0203 a0005c0009t0003g0204 others(1): Show |
4 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-2203G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185911 | |||||||
| chr11:130185924 | C | T | 1 | a0001c0003t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-2190C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185924 | |||||||
| chr11:130185954 | C | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82-2160C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185954 | |||||||
| chr11:130185955 | G | A | 2 | a0002c0011t0003g0209 a0002c0011t0003g0210 |
2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.82-2159G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185955 | |||||||
| chr11:130186059 | C | T | 5 | a0001c0007t0001g0188 a0001c0007t0001g0189 a0001c0007t0003g0190 others(2): Show |
5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-2055C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186059 | |||||||
| chr11:130186223 | CA | C | 4 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1885delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130186223 | ||||||
| chr11:130186342 | A | C | 44 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0001t0004g0196 others(41): Show |
44 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.82-1772A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186342 | |||||||
| chr11:130186479 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.82-1635A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186479 | |||||||
| chr11:130186503 | A | G | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-1611A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186503 | |||||||
| chr11:130186618 | A | G | 1 | a0011c0029t0001g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82-1496A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186618 | |||||||
| chr11:130186787 | C | T | 4 | a0005c0009t0003g0202 a0005c0009t0003g0203 a0005c0009t0003g0204 others(1): Show |
4 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-1327C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186787 | |||||||
| chr11:130186949 | A | G | 5 | a0001c0007t0001g0188 a0001c0007t0001g0189 a0001c0007t0003g0190 others(2): Show |
5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-1165A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186949 | |||||||
| chr11:130187073 | C | T | 1 | a0001c0010t0001g0088 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.82-1041C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187073 | |||||||
| chr11:130187184 | G | A | 7 | a0001c0001t0001g0053 a0001c0001t0002g0005 a0001c0001t0002g0081 others(4): Show |
8 | NA18940.hp2 NA18944.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-930G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187184 | |||||||
| chr11:130187191 | A | AG | 4 | a0001c0007t0001g0117 a0001c0007t0001g0198 a0001c0007t0002g0014 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-922dupG | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130187191 | ||||||
| chr11:130187369 | C | G | 1 | a0003c0005t0001g0124 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.82-745C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187369 | |||||||
| chr11:130187794 | C | T | 3 | a0006c0015t0004g0228 a0006c0015t0004g0230 a0008c0034t0001g0200 |
3 | HG02257.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.82-320C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187794 | |||||||
| chr11:130187839 | C | A | 1 | a0001c0019t0003g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-275C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187839 | |||||||
| chr11:130187864 | T | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-250T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187864 | |||||||
| chr11:130187916 | G | T | 8 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-198G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187916 | |||||||
| chr11:130188002 | C | T | 2 | a0001c0001t0002g0033 a0001c0001t0002g0083 |
2 | HG00621.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.82-112C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130188002 | |||||||
| chr11:130188097 | C | T | 4 | a0004c0030t0001g0187 a0007c0014t0001g0146 a0007c0014t0001g0252 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-17C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130188097 | |||||||
| chr11:130188295 | T | C | 9 | a0001c0007t0001g0188 a0001c0007t0001g0189 a0001c0007t0003g0190 others(6): Show |
9 | HG02280.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+22T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188295 | |||||||
| chr11:130188297 | C | T | 8 | a0001c0019t0003g0205 a0005c0009t0003g0202 a0005c0009t0003g0203 others(5): Show |
8 | HG01261.hp2 HG02257.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.241+24C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188297 | |||||||
| chr11:130188325 | C | T | 1 | a0001c0007t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241+52C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188325 | |||||||
| chr11:130188371 | G | A | 3 | a0001c0016t0002g0106 a0001c0031t0007g0030 a0009c0032t0002g0070 |
3 | HG00735.hp2 HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241+98G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188371 | |||||||
| chr11:130188467 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242-63C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188467 | |||||||
| chr11:130188511 | G | A | 8 | a0001c0019t0003g0205 a0005c0009t0003g0202 a0005c0009t0003g0203 others(5): Show |
8 | HG01261.hp2 HG02257.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-19G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188511 | |||||||
| chr11:130188697 | G | A | 4 | a0001c0007t0001g0188 a0001c0007t0001g0189 a0001c0007t0003g0190 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+40G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/18 | chr11 | 130188697 | |||||||
| chr11:130188754 | T | C | 3 | a0001c0001t0001g0233 a0001c0001t0002g0236 a0001c0002t0001g0235 |
3 | HG01884.hp2 HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.369+97T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/18 | chr11 | 130188754 | |||||||
| chr11:130188790 | T | C | 3 | a0006c0015t0004g0228 a0006c0015t0004g0230 a0008c0034t0001g0200 |
3 | HG02257.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.370-79T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/18 | chr11 | 130188790 | |||||||
| chr11:130189040 | G | A | 1 | a0004c0030t0001g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440+101G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189040 | |||||||
| chr11:130189040 | G | T | 1 | a0001c0007t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.440+101G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189040 | |||||||
| chr11:130189043 | C | T | 16 | a0001c0001t0003g0243 a0001c0002t0001g0241 a0001c0003t0003g0242 others(13): Show |
16 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.440+104C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189043 | |||||||
| chr11:130189066 | T | C | 10 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0007t0001g0104 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.440+127T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189066 | |||||||
| chr11:130189087 | C | T | 11 | a0001c0003t0003g0242 a0001c0003t0005g0143 a0001c0003t0005g0144 others(8): Show |
11 | HG02451.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+148C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189087 | |||||||
| chr11:130189310 | T | C | 1 | a0011c0029t0001g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.440+371T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189310 | |||||||
| chr11:130189607 | G | C | 4 | a0001c0001t0001g0233 a0001c0002t0001g0235 a0001c0023t0001g0232 others(1): Show |
4 | HG01074.hp2 HG01884.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-132G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189607 | |||||||
| chr11:130189633 | A | G | 10 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0007t0001g0104 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.441-106A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189633 | |||||||
| chr11:130189921 | C | T | 5 | a0001c0019t0003g0205 a0004c0030t0001g0187 a0007c0014t0001g0146 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+25C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/18 | chr11 | 130189921 | |||||||
| chr11:130189979 | C | T | 1 | a0001c0003t0001g0195 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.598+83C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/18 | chr11 | 130189979 | |||||||
| chr11:130190045 | A | G | 2 | a0001c0002t0002g0013 a0001c0002t0002g0158 |
3 | HG01361.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.599-68A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/18 | chr11 | 130190045 | |||||||
| chr11:130190216 | C | A | 1 | a0001c0002t0001g0034 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.634+68C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190216 | |||||||
| chr11:130190262 | ACGATCTT others(3): Show |
A | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+115_634+124del others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190262 | |||||||
| chr11:130190275 | G | T | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+127G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190275 | |||||||
| chr11:130190276 | C | A | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+128C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190276 | |||||||
| chr11:130190277 | C | T | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+129C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190277 | |||||||
| chr11:130190278 | C | A | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+130C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190278 | |||||||
| chr11:130190322 | C | T | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.635-132C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190322 | |||||||
| chr11:130190344 | C | T | 9 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-110C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190344 | |||||||
| chr11:130190449 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18992.hp1 | splice_region_variant&intron_variant | LOW | c.635-5C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190449 | |||||||
| chr11:130190706 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0003g0243 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.875+12G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130190706 | |||||||
| chr11:130190717 | A | G | 240 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(237): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.875+23A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130190717 | |||||||
| chr11:130191121 | C | T | 8 | a0001c0019t0003g0205 a0005c0009t0003g0202 a0005c0009t0003g0203 others(5): Show |
8 | HG01261.hp2 HG02257.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+427C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191121 | |||||||
| chr11:130191136 | A | C | 1 | a0001c0028t0001g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.875+442A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191136 | |||||||
| chr11:130191158 | C | A | 1 | a0001c0001t0002g0054 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.875+464C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191158 | |||||||
| chr11:130191163 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0003g0243 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.875+469C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191163 | |||||||
| chr11:130191244 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.875+550G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191244 | |||||||
| chr11:130191264 | C | T | 1 | a0001c0016t0002g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.875+570C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191264 | |||||||
| chr11:130191399 | C | G | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.875+705C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191399 | |||||||
| chr11:130191452 | G | A | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+758G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191452 | |||||||
| chr11:130191460 | C | A | 176 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(173): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.875+766C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191460 | |||||||
| chr11:130191460 | C | T | 2 | a0002c0006t0001g0222 a0002c0006t0001g0226 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.875+766C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191460 | |||||||
| chr11:130191475 | C | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(17): Show |
22 | HG00323.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.875+781C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191475 | |||||||
| chr11:130191516 | C | G | 1 | a0001c0016t0002g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.875+822C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191516 | |||||||
| chr11:130191518 | T | C | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.875+824T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191518 | |||||||
| chr11:130191550 | T | C | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.875+856T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191550 | |||||||
| chr11:130191582 | C | T | 2 | a0001c0023t0001g0232 a0001c0035t0001g0157 |
2 | HG01074.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.875+888C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191582 | |||||||
| chr11:130191668 | C | T | 6 | a0001c0003t0001g0216 a0001c0007t0001g0188 a0001c0007t0001g0189 others(3): Show |
6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+974C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191668 | |||||||
| chr11:130191669 | A | G | 6 | a0001c0003t0001g0216 a0001c0007t0001g0188 a0001c0007t0001g0189 others(3): Show |
6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+975A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191669 | |||||||
| chr11:130191672 | AGAG | A | 6 | a0001c0003t0001g0216 a0001c0007t0001g0188 a0001c0007t0001g0189 others(3): Show |
6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+979_875+981del others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191672 | |||||||
| chr11:130191676 | C | A | 6 | a0001c0003t0001g0216 a0001c0007t0001g0188 a0001c0007t0001g0189 others(3): Show |
6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+982C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191676 | |||||||
| chr11:130191689 | C | CAA | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+1015_875+1016d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | ||||||
| chr11:130191689 | CA | C | 69 | a0001c0001t0001g0229 a0001c0001t0001g0265 a0001c0001t0001g0272 others(66): Show |
69 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.875+1016delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | ||||||
| chr11:130191689 | CAA | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(47): Show |
53 | HG00140.hp2 HG00323.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.875+1015_875+1016d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | ||||||
| chr11:130191689 | CAAA | C | 109 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.875+1014_875+1016d others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | ||||||
| chr11:130191689 | CAAAA | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0043 a0001c0001t0002g0046 others(4): Show |
8 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.875+1013_875+1016d others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | ||||||
| chr11:130191778 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.875+1084T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191778 | |||||||
| chr11:130191852 | G | A | 4 | a0006c0015t0004g0228 a0006c0015t0004g0230 a0008c0022t0001g0071 others(1): Show |
4 | HG02257.hp1 HG03654.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+1158G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191852 | |||||||
| chr11:130191868 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.875+1174C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191868 | |||||||
| chr11:130191892 | G | A | 229 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.875+1198G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191892 | |||||||
| chr11:130191918 | G | A | 1 | a0013c0024t0001g0055 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.875+1224G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191918 | |||||||
| chr11:130192069 | G | A | 1 | a0001c0003t0005g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.875+1375G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192069 | |||||||
| chr11:130192224 | C | T | 249 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.875+1530C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192224 | |||||||
| chr11:130192240 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.875+1546G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192240 | |||||||
| chr11:130192302 | A | G | 2 | a0007c0014t0001g0146 a0007c0014t0001g0252 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.875+1608A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192302 | |||||||
| chr11:130192402 | T | C | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.875+1708T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192402 | |||||||
| chr11:130192465 | C | T | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.876-1684C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192465 | |||||||
| chr11:130192492 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.876-1657G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192492 | |||||||
| chr11:130192514 | G | A | 1 | a0001c0003t0002g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.876-1635G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192514 | |||||||
| chr11:130192588 | T | C | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.876-1561T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192588 | |||||||
| chr11:130192806 | G | A | 243 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.876-1343G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192806 | |||||||
| chr11:130192875 | C | A | 1 | a0004c0008t0004g0169 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.876-1274C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192875 | |||||||
| chr11:130192898 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.876-1251G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192898 | |||||||
| chr11:130193103 | G | GT | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.876-1035dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193103 | ||||||
| chr11:130193103 | G | GTT | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0003 others(2): Show |
6 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-1036_876-1035d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193103 | ||||||
| chr11:130193232 | C | T | 243 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.876-917C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193232 | |||||||
| chr11:130193245 | G | A | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-904G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193245 | |||||||
| chr11:130193338 | A | G | 1 | a0001c0003t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.876-811A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193338 | |||||||
| chr11:130193357 | C | T | 243 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.876-792C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193357 | |||||||
| chr11:130193366 | G | A | 73 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0044 others(70): Show |
74 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.876-783G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193366 | |||||||
| chr11:130193476 | C | CT | 56 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0044 others(53): Show |
57 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.876-660dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193476 | ||||||
| chr11:130193490 | C | G | 12 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(9): Show |
12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-659C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193490 | |||||||
| chr11:130193601 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876-548C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193601 | |||||||
| chr11:130193626 | T | C | 243 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.876-523T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193626 | |||||||
| chr11:130193643 | T | C | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.876-506T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193643 | |||||||
| chr11:130193684 | G | A | 1 | a0001c0001t0002g0035 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.876-465G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193684 | |||||||
| chr11:130193754 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.876-395G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193754 | |||||||
| chr11:130193762 | G | T | 2 | a0007c0014t0001g0146 a0007c0014t0001g0252 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.876-387G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193762 | |||||||
| chr11:130193782 | T | TTGATTGT others(85): Show |
12 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(9): Show |
12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-266_876-175dup others(92): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | ||||||
| chr11:130193782 | T | TTGATTGT others(131): Show |
76 | a0001c0001t0001g0015 a0001c0001t0002g0006 a0001c0001t0002g0018 others(73): Show |
78 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.876-312_876-175dup others(138): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | ||||||
| chr11:130193782 | T | TTGATTGT others(177): Show |
152 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(149): Show |
163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.876-358_876-175dup others(184): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | ||||||
| chr11:130193782 | T | TTGATTGT others(223): Show |
1 | a0001c0001t0003g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876-175_876-174ins others(230): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | ||||||
| chr11:130193782 | TTGATTGT others(39): Show |
T | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-220_876-175del others(46): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | ||||||
| chr11:130193838 | C | CAAAGGTG others(39): Show |
2 | a0007c0014t0001g0146 a0007c0014t0001g0252 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.876-266_876-265ins others(46): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193838 | ||||||
| chr11:130193863 | G | A | 1 | a0001c0007t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.876-286G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193863 | |||||||
| chr11:130194144 | C | G | 1 | a0001c0002t0001g0245 | 1 | NA18967.hp2 | splice_region_variant&intron_variant | LOW | c.876-5C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130194144 | |||||||
| chr11:130194328 | A | G | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1015+40A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/18 | chr11 | 130194328 | |||||||
| chr11:130194486 | G | A | 1 | a0001c0003t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1016-154G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/18 | chr11 | 130194486 | |||||||
| chr11:130194559 | C | A | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1016-81C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/18 | chr11 | 130194559 | |||||||
| chr11:130194752 | G | A | 226 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(223): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1113+15G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194752 | |||||||
| chr11:130194804 | CTGTGCAG others(3): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1113+72_1113+81del others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194804 | ||||||
| chr11:130194809 | C | T | 2 | a0001c0002t0002g0257 a0001c0002t0002g0268 |
2 | HG04115.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1113+72C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194809 | |||||||
| chr11:130194810 | A | G | 257 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(254): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1113+73A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194810 | |||||||
| chr11:130194851 | C | CAT | 12 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(9): Show |
12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+115_1113+116d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194851 | ||||||
| chr11:130194851 | C | CGT | 13 | a0001c0002t0001g0235 a0001c0003t0001g0041 a0001c0003t0001g0065 others(10): Show |
13 | HG01109.hp2 HG01517.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+114_1113+115i others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194851 | |||||||
| chr11:130194852 | A | G | 69 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0044 others(66): Show |
70 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1113+115A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194852 | |||||||
| chr11:130194852 | ATG | A | 5 | a0001c0019t0003g0205 a0006c0015t0004g0228 a0006c0015t0004g0230 others(2): Show |
5 | HG02257.hp1 HG03041.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+138_1113+139d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194852 | ||||||
| chr11:130194852 | ATGTG | A | 7 | a0001c0001t0001g0233 a0005c0009t0002g0217 a0005c0009t0002g0220 others(4): Show |
7 | HG01261.hp2 HG02109.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+136_1113+139d others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194852 | ||||||
| chr11:130194852 | ATGTGTGT others(1): Show |
A | 157 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(154): Show |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1113+132_1113+139d others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194852 | ||||||
| chr11:130194875 | T | C | 3 | a0001c0003t0001g0016 a0001c0003t0001g0195 a0001c0003t0001g0263 |
3 | HG00642.hp1 HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1113+138T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194875 | |||||||
| chr11:130195079 | C | T | 228 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1113+342C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195079 | |||||||
| chr11:130195466 | G | A | 4 | a0006c0015t0004g0228 a0006c0015t0004g0230 a0008c0022t0001g0071 others(1): Show |
4 | HG02257.hp1 HG03654.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+729G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195466 | |||||||
| chr11:130195542 | C | T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0195 |
2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1114-797C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195542 | |||||||
| chr11:130195581 | G | T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0195 |
2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1114-758G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195581 | |||||||
| chr11:130195637 | G | A | 240 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(237): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1114-702G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195637 | |||||||
| chr11:130195721 | C | T | 1 | a0001c0002t0001g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1114-618C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195721 | |||||||
| chr11:130195777 | C | T | 6 | a0005c0009t0002g0217 a0005c0009t0002g0220 a0005c0009t0003g0202 others(3): Show |
6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-562C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195777 | |||||||
| chr11:130195801 | T | C | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1114-538T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195801 | |||||||
| chr11:130195802 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1114-537G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195802 | |||||||
| chr11:130195843 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0068 |
2 | NA18964.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1114-496A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195843 | |||||||
| chr11:130195851 | TCA | T | 225 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(222): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1114-487_1114-486d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195851 | |||||||
| chr11:130195852 | CAA | C | 12 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(9): Show |
12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1114-473_1114-472d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130195852 | ||||||
| chr11:130195871 | A | T | 4 | a0001c0003t0003g0242 a0001c0003t0005g0143 a0001c0003t0005g0144 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-468A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195871 | |||||||
| chr11:130195876 | G | T | 240 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(237): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1114-463G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195876 | |||||||
| chr11:130195893 | G | C | 1 | a0001c0001t0002g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1114-446G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195893 | |||||||
| chr11:130195928 | G | A | 9 | a0001c0001t0001g0233 a0001c0023t0001g0232 a0001c0035t0001g0157 others(6): Show |
9 | HG01074.hp2 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-411G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195928 | |||||||
| chr11:130196194 | C | A | 235 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1114-145C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130196194 | |||||||
| chr11:130196194 | C | CAAAA | 13 | a0001c0001t0002g0033 a0004c0008t0001g0161 a0004c0008t0001g0171 others(10): Show |
13 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1114-144_1114-143i others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130196194 | ||||||
| chr11:130196273 | T | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(12): Show |
18 | HG00408.hp1 HG02559.hp2 HG03540.hp1 others(15): Show |
intron_variant | MODIFIER | c.1114-66T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130196273 | |||||||
| chr11:130196477 | G | A | 250 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1223+29G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | chr11 | 130196477 | |||||||
| chr11:130196523 | C | T | 11 | a0001c0001t0001g0233 a0001c0001t0004g0196 a0001c0001t0004g0197 others(8): Show |
11 | HG01074.hp2 HG01261.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1224-47C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | chr11 | 130196523 | |||||||
| chr11:130196557 | G | GC | 177 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
splice_region_variant&intron_variant | LOW | c.1224-6dupC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr11 | 130196557 | ||||||
| chr11:130196565 | T | C | 7 | a0003c0005t0001g0008 a0003c0005t0001g0027 a0003c0005t0001g0080 others(4): Show |
7 | HG00639.hp1 HG01106.hp1 HG01243.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1224-5T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | chr11 | 130196565 | |||||||
| chr11:130196893 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0063 |
3 | HG01069.hp2 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1354+193C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130196893 | |||||||
| chr11:130196972 | T | C | 229 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1354+272T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130196972 | |||||||
| chr11:130196976 | C | T | 229 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1354+276C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130196976 | |||||||
| chr11:130197005 | C | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(128): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1354+305C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197005 | |||||||
| chr11:130197007 | G | A | 229 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1354+307G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197007 | |||||||
| chr11:130197062 | C | T | 228 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1354+362C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197062 | |||||||
| chr11:130197174 | G | C | 219 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1354+474G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197174 | |||||||
| chr11:130197288 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1355-553C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197288 | |||||||
| chr11:130197331 | G | A | 206 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(203): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1355-510G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197331 | |||||||
| chr11:130197663 | G | A | 1 | a0004c0008t0004g0169 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1355-178G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197663 | |||||||
| chr11:130197982 | C | T | 14 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0002g0033 others(11): Show |
14 | HG00621.hp2 HG00639.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1459+37C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130197982 | |||||||
| chr11:130197997 | C | T | 89 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(86): Show |
92 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1459+52C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130197997 | |||||||
| chr11:130198026 | C | T | 2 | a0005c0009t0003g0203 a0005c0009t0003g0204 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1459+81C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198026 | |||||||
| chr11:130198092 | A | C | 86 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(83): Show |
89 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1459+147A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198092 | |||||||
| chr11:130198110 | T | C | 1 | a0002c0004t0002g0223 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1459+165T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198110 | |||||||
| chr11:130198119 | T | TATGGCAG others(1): Show |
4 | a0001c0003t0003g0242 a0001c0003t0005g0143 a0001c0003t0005g0144 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+174_1459+175i others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198119 | |||||||
| chr11:130198120 | G | T | 4 | a0001c0003t0003g0242 a0001c0003t0005g0143 a0001c0003t0005g0144 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+175G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198120 | |||||||
| chr11:130198465 | A | G | 3 | a0001c0002t0003g0052 a0007c0014t0001g0146 a0007c0014t0001g0252 |
3 | HG01255.hp1 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1571-43A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/18 | chr11 | 130198465 | |||||||
| chr11:130198470 | C | T | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1571-38C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/18 | chr11 | 130198470 | |||||||
| chr11:130198628 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0002g0037 a0001c0001t0002g0083 |
3 | HG00621.hp1 HG02074.hp2 NA19074.hp1 |
splice_region_variant&intron_variant | LOW | c.1684+7C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/18 | chr11 | 130198628 | |||||||
| chr11:130198659 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(129): Show |
142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1684+38C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/18 | chr11 | 130198659 | |||||||
| chr11:130198688 | C | T | 3 | a0001c0001t0002g0061 a0008c0034t0001g0200 a0012c0021t0002g0038 |
3 | HG03017.hp2 HG04199.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1684+67C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/18 | chr11 | 130198688 | |||||||
| chr11:130199153 | C | T | 1 | a0001c0003t0005g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1807+84C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199153 | |||||||
| chr11:130199250 | C | T | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1807+181C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199250 | |||||||
| chr11:130199291 | A | G | 17 | a0001c0003t0001g0016 a0001c0003t0001g0041 a0001c0003t0001g0167 others(14): Show |
17 | HG01099.hp1 HG01517.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1807+222A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199291 | |||||||
| chr11:130199299 | G | A | 1 | a0001c0019t0003g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1807+230G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199299 | |||||||
| chr11:130199623 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1808-328A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199623 | |||||||
| chr11:130199661 | G | A | 151 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1808-290G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199661 | |||||||
| chr11:130199679 | G | A | 3 | a0001c0002t0001g0235 a0004c0008t0001g0161 a0004c0008t0001g0171 |
3 | HG01884.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1808-272G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199679 | |||||||
| chr11:130199743 | G | A | 3 | a0001c0001t0002g0069 a0001c0001t0002g0112 a0001c0001t0002g0129 |
3 | HG00140.hp1 HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1808-208G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199743 | |||||||
| chr11:130199775 | T | C | 10 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1808-176T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199775 | |||||||
| chr11:130199809 | C | T | 157 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(154): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1808-142C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199809 | |||||||
| chr11:130199865 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1808-86G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199865 | |||||||
| chr11:130200298 | T | C | 2 | a0007c0014t0001g0146 a0007c0014t0001g0252 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1994+161T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200298 | |||||||
| chr11:130200350 | G | A | 2 | a0007c0014t0001g0146 a0007c0014t0001g0252 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1994+213G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200350 | |||||||
| chr11:130200560 | C | A | 1 | a0001c0002t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1994+423C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200560 | |||||||
| chr11:130200637 | C | T | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1994+500C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200637 | |||||||
| chr11:130200649 | G | A | 150 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(147): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1994+512G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200649 | |||||||
| chr11:130200905 | C | T | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1994+768C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200905 | |||||||
| chr11:130201004 | A | G | 34 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(31): Show |
36 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1994+867A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201004 | |||||||
| chr11:130201133 | A | G | 203 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(200): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1994+996A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201133 | |||||||
| chr11:130201189 | C | T | 2 | a0004c0008t0001g0161 a0004c0008t0001g0171 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1994+1052C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201189 | |||||||
| chr11:130201290 | A | G | 13 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(10): Show |
13 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1994+1153A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201290 | |||||||
| chr11:130201298 | A | G | 13 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(10): Show |
13 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1994+1161A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201298 | |||||||
| chr11:130201324 | C | T | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1187C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201324 | |||||||
| chr11:130201358 | G | T | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1221G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201358 | |||||||
| chr11:130201398 | G | A | 13 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(10): Show |
13 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1994+1261G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201398 | |||||||
| chr11:130201442 | G | T | 8 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1994+1305G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201442 | |||||||
| chr11:130201450 | G | A | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1313G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201450 | |||||||
| chr11:130201704 | T | C | 147 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(144): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1994+1567T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201704 | |||||||
| chr11:130201795 | C | T | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1658C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201795 | |||||||
| chr11:130201925 | C | A | 1 | a0002c0006t0001g0156 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1994+1788C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201925 | |||||||
| chr11:130202074 | T | G | 3 | a0001c0003t0001g0016 a0001c0003t0001g0065 a0001c0003t0001g0195 |
3 | HG00735.hp1 HG01109.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1994+1937T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202074 | |||||||
| chr11:130202198 | G | A | 6 | a0004c0008t0001g0161 a0004c0008t0001g0171 a0004c0008t0004g0168 others(3): Show |
6 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1994+2061G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202198 | |||||||
| chr11:130202203 | G | A | 2 | a0001c0001t0001g0067 a0001c0003t0001g0041 |
2 | HG01517.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1994+2066G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202203 | |||||||
| chr11:130202462 | T | A | 1 | a0001c0001t0002g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1994+2325T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202462 | |||||||
| chr11:130202489 | G | A | 33 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(30): Show |
35 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1994+2352G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202489 | |||||||
| chr11:130202631 | A | G | 5 | a0001c0002t0003g0052 a0001c0003t0001g0016 a0001c0003t0001g0041 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1994+2494A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202631 | |||||||
| chr11:130202674 | C | T | 7 | a0002c0006t0001g0226 a0004c0008t0001g0161 a0004c0008t0001g0171 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1994+2537C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202674 | |||||||
| chr11:130202685 | T | C | 195 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(192): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1994+2548T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202685 | |||||||
| chr11:130202702 | C | T | 1 | a0003c0005t0001g0124 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1994+2565C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202702 | |||||||
| chr11:130202715 | C | A | 1 | a0001c0003t0005g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1994+2578C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202715 | |||||||
| chr11:130202739 | G | A | 14 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(11): Show |
14 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1994+2602G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202739 | |||||||
| chr11:130202836 | A | G | 18 | a0001c0002t0003g0052 a0001c0003t0001g0016 a0001c0003t0001g0041 others(15): Show |
18 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1994+2699A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202836 | |||||||
| chr11:130202888 | G | C | 18 | a0001c0002t0003g0052 a0001c0003t0001g0016 a0001c0003t0001g0041 others(15): Show |
18 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1994+2751G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202888 | |||||||
| chr11:130203023 | A | G | 14 | a0001c0002t0001g0235 a0001c0003t0001g0167 a0001c0007t0001g0104 others(11): Show |
14 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1994+2886A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203023 | |||||||
| chr11:130203171 | C | T | 5 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0041 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1994+3034C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203171 | |||||||
| chr11:130203446 | C | T | 1 | a0001c0002t0002g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1994+3309C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203446 | |||||||
| chr11:130203460 | C | T | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3323C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203460 | |||||||
| chr11:130203638 | A | G | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3501A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203638 | |||||||
| chr11:130203643 | T | C | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3506T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203643 | |||||||
| chr11:130203647 | T | C | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3510T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203647 | |||||||
| chr11:130203675 | C | T | 2 | a0001c0003t0001g0173 a0001c0003t0001g0263 |
2 | HG00642.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1994+3538C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203675 | |||||||
| chr11:130203735 | C | T | 4 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(1): Show |
4 | HG01255.hp1 HG01517.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994+3598C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203735 | |||||||
| chr11:130203770 | A | G | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1994+3633A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203770 | |||||||
| chr11:130203809 | T | C | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3672T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203809 | |||||||
| chr11:130203819 | A | G | 1 | a0002c0006t0001g0214 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1994+3682A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203819 | |||||||
| chr11:130203842 | C | T | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3705C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203842 | |||||||
| chr11:130203843 | G | A | 3 | a0003c0005t0001g0123 a0003c0005t0001g0124 a0003c0005t0002g0025 |
3 | HG01934.hp2 HG01952.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1994+3706G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203843 | |||||||
| chr11:130203887 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1994+3750C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203887 | |||||||
| chr11:130203888 | G | A | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3751G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203888 | |||||||
| chr11:130203953 | C | A | 8 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(5): Show |
8 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1994+3816C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203953 | |||||||
| chr11:130204018 | C | T | 8 | a0001c0001t0001g0276 a0001c0002t0001g0207 a0001c0002t0001g0208 others(5): Show |
8 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1994+3881C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204018 | |||||||
| chr11:130204121 | G | A | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1994+3984G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204121 | |||||||
| chr11:130204182 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1994+4045T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204182 | |||||||
| chr11:130204242 | G | A | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1994+4105G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204242 | |||||||
| chr11:130204295 | A | G | 178 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(175): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1995-4115A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204295 | |||||||
| chr11:130204376 | C | A | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-4034C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204376 | |||||||
| chr11:130204433 | A | C | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3977A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204433 | |||||||
| chr11:130204497 | G | T | 4 | a0001c0003t0003g0242 a0001c0003t0005g0143 a0001c0003t0005g0144 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995-3913G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204497 | |||||||
| chr11:130204540 | G | A | 5 | a0001c0001t0001g0276 a0001c0003t0001g0016 a0001c0003t0001g0041 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995-3870G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204540 | |||||||
| chr11:130204587 | A | G | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3823A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204587 | |||||||
| chr11:130204599 | G | T | 2 | a0001c0002t0001g0240 a0001c0002t0001g0241 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1995-3811G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204599 | |||||||
| chr11:130204685 | A | T | 1 | a0001c0003t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1995-3725A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204685 | |||||||
| chr11:130204704 | T | TA | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3706_1995-370 others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204704 | |||||||
| chr11:130205043 | T | C | 5 | a0001c0001t0001g0229 a0001c0003t0003g0242 a0001c0003t0005g0143 others(2): Show |
5 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995-3367T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205043 | |||||||
| chr11:130205108 | T | C | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3302T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205108 | |||||||
| chr11:130205159 | A | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(180): Show |
192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1995-3251A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205159 | |||||||
| chr11:130205370 | C | A | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3040C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205370 | |||||||
| chr11:130205372 | C | G | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3038C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205372 | |||||||
| chr11:130205374 | T | C | 178 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(175): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1995-3036T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205374 | |||||||
| chr11:130205375 | G | A | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3035G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205375 | |||||||
| chr11:130205377 | C | G | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3033C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205377 | |||||||
| chr11:130205378 | T | A | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3032T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205378 | |||||||
| chr11:130205379 | T | C | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3031T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205379 | |||||||
| chr11:130205381 | G | A | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3029G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205381 | |||||||
| chr11:130205382 | C | T | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3028C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205382 | |||||||
| chr11:130205383 | C | G | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3027C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205383 | |||||||
| chr11:130205386 | C | T | 1 | a0003c0005t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3024C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205386 | |||||||
| chr11:130205481 | C | T | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1995-2929C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205481 | |||||||
| chr11:130205537 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(19): Show |
24 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1995-2873G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205537 | |||||||
| chr11:130205539 | G | A | 157 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(154): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1995-2871G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205539 | |||||||
| chr11:130205653 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1995-2757C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205653 | |||||||
| chr11:130205666 | C | T | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1995-2744C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205666 | |||||||
| chr11:130205680 | A | G | 124 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0094 others(121): Show |
131 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1995-2730A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205680 | |||||||
| chr11:130205683 | A | G | 2 | a0001c0002t0001g0050 a0001c0002t0001g0274 |
2 | NA18971.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1995-2727A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205683 | |||||||
| chr11:130205699 | G | GT | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(41): Show |
46 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1995-2700dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130205699 | ||||||
| chr11:130205699 | G | GTT | 10 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0109 others(7): Show |
10 | HG00438.hp2 HG00642.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1995-2701_1995-270 others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130205699 | ||||||
| chr11:130205706 | T | G | 2 | a0005c0009t0002g0217 a0005c0009t0002g0220 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1995-2704T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205706 | |||||||
| chr11:130205709 | T | G | 1 | a0001c0019t0003g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1995-2701T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205709 | |||||||
| chr11:130205710 | T | G | 1 | a0001c0031t0007g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1995-2700T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205710 | |||||||
| chr11:130205710 | TG | T | 97 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0058 others(94): Show |
102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1995-2699delG | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205710 | |||||||
| chr11:130205711 | G | T | 181 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
185 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1995-2699G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205711 | |||||||
| chr11:130205728 | G | A | 6 | a0001c0001t0001g0276 a0001c0001t0002g0035 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1995-2682G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205728 | |||||||
| chr11:130205741 | C | T | 201 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(198): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1995-2669C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205741 | |||||||
| chr11:130205829 | G | A | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995-2581G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205829 | |||||||
| chr11:130205855 | C | T | 34 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(31): Show |
36 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1995-2555C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205855 | |||||||
| chr11:130205857 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1995-2553C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205857 | |||||||
| chr11:130205888 | G | A | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995-2522G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205888 | |||||||
| chr11:130205965 | A | G | 9 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(6): Show |
9 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1995-2445A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205965 | |||||||
| chr11:130205972 | C | T | 3 | a0001c0001t0001g0233 a0001c0023t0001g0232 a0001c0035t0001g0157 |
3 | HG01074.hp2 HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1995-2438C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205972 | |||||||
| chr11:130206120 | G | T | 1 | a0005c0009t0003g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1995-2290G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206120 | |||||||
| chr11:130206230 | C | T | 1 | a0001c0003t0001g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1995-2180C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206230 | |||||||
| chr11:130206231 | G | A | 4 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0004c0008t0004g0237 others(1): Show |
4 | HG01109.hp1 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1995-2179G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206231 | |||||||
| chr11:130206237 | G | A | 7 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(4): Show |
7 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995-2173G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206237 | |||||||
| chr11:130206311 | G | A | 11 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0004t0001g0194 others(8): Show |
11 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995-2099G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206311 | |||||||
| chr11:130206390 | A | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(2): Show |
7 | HG00408.hp1 HG02080.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995-2020A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206390 | |||||||
| chr11:130206395 | C | T | 1 | a0003c0005t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1995-2015C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206395 | |||||||
| chr11:130206395 | CGTGA | C | 114 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0148 others(111): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1995-2011_1995-200 others(8): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130206395 | ||||||
| chr11:130206439 | C | T | 114 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0148 others(111): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1995-1971C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206439 | |||||||
| chr11:130206443 | C | T | 1 | a0001c0003t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1995-1967C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206443 | |||||||
| chr11:130206460 | T | TG | 6 | a0001c0001t0001g0276 a0001c0002t0003g0052 a0001c0003t0001g0016 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-1950_1995-194 others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206460 | |||||||
| chr11:130206567 | C | CT | 149 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0148 others(146): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1995-1832dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130206567 | ||||||
| chr11:130206648 | AC | A | 114 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0148 others(111): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1995-1760delC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130206648 | ||||||
| chr11:130206757 | G | A | 2 | a0006c0015t0004g0228 a0006c0015t0004g0230 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1995-1653G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206757 | |||||||
| chr11:130206807 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1995-1603A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206807 | |||||||
| chr11:130206887 | T | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(9): Show |
14 | HG00408.hp1 HG02080.hp2 HG03831.hp1 others(11): Show |
intron_variant | MODIFIER | c.1995-1523T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206887 | |||||||
| chr11:130206999 | G | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(25): Show |
31 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1995-1411G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206999 | |||||||
| chr11:130207063 | G | A | 12 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0002c0006t0001g0212 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1995-1347G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207063 | |||||||
| chr11:130207065 | A | G | 2 | a0001c0002t0001g0034 a0001c0002t0001g0259 |
2 | HG02040.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1995-1345A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207065 | |||||||
| chr11:130207071 | G | A | 10 | a0001c0003t0001g0167 a0001c0007t0001g0104 a0002c0006t0001g0211 others(7): Show |
10 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1995-1339G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207071 | |||||||
| chr11:130207128 | C | T | 203 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(200): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1995-1282C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207128 | |||||||
| chr11:130207231 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1995-1179C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207231 | |||||||
| chr11:130207372 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(14): Show |
19 | HG00408.hp1 HG00642.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1995-1038G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207372 | |||||||
| chr11:130207615 | C | G | 1 | a0009c0032t0002g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1995-795C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207615 | |||||||
| chr11:130207760 | G | C | 2 | a0001c0003t0001g0173 a0001c0003t0001g0263 |
2 | HG00642.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1995-650G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207760 | |||||||
| chr11:130207899 | C | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(23): Show |
28 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1995-511C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207899 | |||||||
| chr11:130207945 | C | T | 2 | a0001c0001t0002g0089 a0001c0001t0002g0113 |
2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1995-465C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207945 | |||||||
| chr11:130208020 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1995-390G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208020 | |||||||
| chr11:130208073 | CAATAAAT others(1): Show |
C | 27 | a0001c0001t0001g0155 a0001c0001t0002g0004 a0001c0001t0002g0007 others(24): Show |
30 | HG00735.hp2 HG01069.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1995-321_1995-314d others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130208073 | ||||||
| chr11:130208194 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1995-216G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208194 | |||||||
| chr11:130208281 | G | A | 7 | a0002c0006t0001g0211 a0002c0006t0001g0213 a0002c0006t0001g0214 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995-129G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208281 | |||||||
| chr11:130208372 | G | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1995-38G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208372 | |||||||
| chr11:130208850 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2269+166A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130208850 | |||||||
| chr11:130208894 | C | T | 1 | a0001c0003t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2269+210C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130208894 | |||||||
| chr11:130208899 | C | G | 1 | a0001c0002t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2269+215C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130208899 | |||||||
| chr11:130209115 | A | C | 1 | a0001c0001t0002g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2270-327A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209115 | |||||||
| chr11:130209199 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0023t0001g0232 |
3 | HG01074.hp2 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2270-243C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209199 | |||||||
| chr11:130209215 | G | A | 1 | a0001c0002t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2270-227G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209215 | |||||||
| chr11:130209320 | T | G | 21 | a0001c0001t0001g0155 a0001c0003t0001g0032 a0001c0003t0001g0167 others(18): Show |
21 | HG01069.hp1 HG01099.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.2270-122T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209320 | |||||||
| chr11:130209339 | G | C | 121 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0265 others(118): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2270-103G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209339 | |||||||
| chr11:130209582 | G | C | 1 | a0001c0002t0001g0235 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.2406+4G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 18/18 | chr11 | 130209582 |