Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57661 |
| ensemblid | ENSG00000070047.13 |
| hgncid | 24351 |
| symbol | PHRF1 |
| name | PHD and ring finger domains 1 |
| refseq_nuc | NM_001286581.2 |
| refseq_prot | NP_001273510.1 |
| ensembl_nuc | ENST00000264555.10 |
| ensembl_prot | ENSP00000264555.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 576470 |
| end | 612222 |
| strand | + |
| ver | v1.2 |
| region | chr11:576470-612222 |
| region5000 | chr11:571470-617222 |
| regionname0 | PHRF1_chr11_576470_612222 |
| regionname5000 | PHRF1_chr11_571470_617222 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1649 | 149 | 33 | 32 | 54 | 9 | 20 | 34 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0002 | 0/0 | 1649 | 63 | 15 | 10 | 32 | 1 | 5 | 18 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0003 | 0/0 | 1645 | 19 | 14 | 5 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1640): Show |
chr11 | 571470 | 617222 |
| a0004 | 0/0 | 1649 | 10 | 0 | 9 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0005 | 0/0 | 1649 | 8 | 0 | 2 | 1 | 1 | 4 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0006 | 0/0 | 1649 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0007 | 0/0 | 1645 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1640): Show |
chr11 | 571470 | 617222 |
| a0008 | 0/0 | 1649 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0009 | 0/0 | 1649 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0010 | 0/0 | 1649 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0011 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0012 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0013 | 0/0 | 1645 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1640): Show |
chr11 | 571470 | 617222 |
| a0014 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0015 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0016 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0017 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0018 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0019 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0020 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0021 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0022 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| a0023 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | MDDDS others(1644): Show |
chr11 | 571470 | 617222 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4947 | 95 | 7 | 19 | 48 | 4 | 17 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0003 | 0/1 | 4947 | 29 | 11 | 10 | 3 | 2 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0006 | 0/0 | 4947 | 9 | 7 | 1 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0009 | 0/0 | 4947 | 5 | 4 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0014 | 0/0 | 4947 | 3 | 2 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0018 | 0/0 | 4947 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0023 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0025 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0027 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0031 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0033 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0001c0034 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0002c0002 | 0/0 | 4947 | 59 | 11 | 10 | 32 | 1 | 5 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0002c0011 | 0/0 | 4947 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0003c0004 | 0/0 | 4935 | 12 | 7 | 5 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4930): Show |
chr11 | 571470 | 617222 | ||
| a0003c0008 | 0/0 | 4935 | 6 | 6 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4930): Show |
chr11 | 571470 | 617222 | ||
| a0003c0020 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4930): Show |
chr11 | 571470 | 617222 | ||
| a0004c0005 | 0/0 | 4947 | 10 | 0 | 9 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0005c0007 | 0/0 | 4947 | 8 | 0 | 2 | 1 | 1 | 4 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0006c0010 | 0/0 | 4947 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0007c0012 | 0/0 | 4935 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4930): Show |
chr11 | 571470 | 617222 | ||
| a0008c0013 | 0/0 | 4947 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0009c0015 | 0/0 | 4947 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0010c0019 | 0/0 | 4947 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0011c0017 | 0/0 | 4947 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0012c0016 | 0/0 | 4947 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0013c0021 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4930): Show |
chr11 | 571470 | 617222 | ||
| a0013c0022 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4930): Show |
chr11 | 571470 | 617222 | ||
| a0014c0030 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0015c0036 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0016c0029 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0017c0038 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0018c0037 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0019c0028 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0020c0032 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0021c0035 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0022c0026 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 | ||
| a0023c0024 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | ATGGA others(4942): Show |
chr11 | 571470 | 617222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5539 | 95 | 7 | 19 | 48 | 4 | 17 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0003t0002 | 0/0 | 5539 | 27 | 11 | 10 | 2 | 2 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0003t0008 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0003t0009 | 0/1 | 5539 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0006t0002 | 0/0 | 5539 | 9 | 7 | 1 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0009t0002 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0009t0007 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0014t0001 | 0/0 | 5539 | 3 | 2 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0018t0001 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0023t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0025t0002 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0027t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0031t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0033t0010 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0001c0034t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0002c0002t0001 | 0/0 | 5539 | 59 | 11 | 10 | 32 | 1 | 5 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0002c0011t0001 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0003c0004t0003 | 0/0 | 5527 | 12 | 7 | 5 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5522): Show |
chr11 | 571470 | 617222 |
| a0003c0008t0004 | 0/0 | 5527 | 5 | 5 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5522): Show |
chr11 | 571470 | 617222 |
| a0003c0008t0005 | 0/0 | 5449 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5444): Show |
chr11 | 571470 | 617222 |
| a0003c0020t0006 | 0/0 | 5527 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5522): Show |
chr11 | 571470 | 617222 |
| a0004c0005t0002 | 0/0 | 5539 | 10 | 0 | 9 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0005c0007t0001 | 0/0 | 5539 | 8 | 0 | 2 | 1 | 1 | 4 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0006c0010t0002 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0007c0012t0003 | 0/0 | 5527 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5522): Show |
chr11 | 571470 | 617222 |
| a0008c0013t0002 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0009c0015t0001 | 0/0 | 5539 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0010c0019t0001 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0011c0017t0001 | 0/0 | 5539 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0012c0016t0001 | 0/0 | 5539 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0013c0021t0002 | 0/0 | 5527 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5522): Show |
chr11 | 571470 | 617222 |
| a0013c0022t0002 | 0/0 | 5527 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5522): Show |
chr11 | 571470 | 617222 |
| a0014c0030t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0015c0036t0001 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0016c0029t0001 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0017c0038t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0018c0037t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0019c0028t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0020c0032t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0021c0035t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0022c0026t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| a0023c0024t0002 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | GCACT others(5534): Show |
chr11 | 571470 | 617222 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0003t0009g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0006t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0009t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0009t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0009t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0009t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0009t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0014t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0014t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0014t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0018t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0018t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0023t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0025t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0027t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0031t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0033t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0001c0034t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0011t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0011t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0002c0011t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0008t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0008t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0008t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0008t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0008t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0008t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0003c0020t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0004c0005t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0005c0007t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0006c0010t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0006c0010t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0006c0010t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0006c0010t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0007c0012t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0007c0012t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0007c0012t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0008c0013t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0008c0013t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0009c0015t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0010c0019t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0010c0019t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0011c0017t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0011c0017t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0012c0016t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0012c0016t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0013c0021t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0013c0022t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0014c0030t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0015c0036t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0016c0029t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0017c0038t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0018c0037t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0019c0028t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0020c0032t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0021c0035t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0022c0026t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| a0023c0024t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0005 | t0002 | g0044 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00099 | hp2 | a0001 | c0027 | t0001 | g0253 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00140 | hp1 | a0001 | c0006 | t0002 | g0125 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0217 | EUR | FIN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00544 | hp2 | a0014 | c0030 | t0001 | g0181 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00639 | hp2 | a0003 | c0004 | t0003 | g0084 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0052 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0028 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01074 | hp1 | a0001 | c0009 | t0007 | g0098 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0045 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01106 | hp2 | a0015 | c0036 | t0001 | g0111 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01168 | hp1 | a0003 | c0004 | t0003 | g0006 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01168 | hp2 | a0005 | c0007 | t0001 | g0178 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01169 | hp1 | a0003 | c0004 | t0003 | g0006 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01175 | hp1 | a0004 | c0005 | t0002 | g0035 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01192 | hp1 | a0001 | c0006 | t0002 | g0017 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0015 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01243 | hp2 | a0016 | c0029 | t0001 | g0216 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0030 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01256 | hp2 | a0009 | c0015 | t0001 | g0004 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0029 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01257 | hp2 | a0004 | c0005 | t0002 | g0025 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01258 | hp1 | a0004 | c0005 | t0002 | g0034 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01258 | hp2 | a0009 | c0015 | t0001 | g0004 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01346 | hp1 | a0003 | c0004 | t0003 | g0221 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01346 | hp2 | a0004 | c0005 | t0002 | g0036 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0031 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01433 | hp2 | a0003 | c0004 | t0003 | g0085 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0055 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0056 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01884 | hp2 | a0003 | c0004 | t0003 | g0215 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01891 | hp1 | a0006 | c0010 | t0002 | g0012 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01928 | hp2 | a0004 | c0005 | t0002 | g0043 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01943 | hp2 | a0001 | c0014 | t0001 | g0261 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01975 | hp2 | a0004 | c0005 | t0002 | g0033 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01981 | hp2 | a0004 | c0005 | t0002 | g0019 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02004 | hp2 | a0005 | c0007 | t0001 | g0252 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02015 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02040 | hp1 | a0010 | c0019 | t0001 | g0127 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02056 | hp1 | a0005 | c0007 | t0001 | g0179 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02083 | hp1 | a0010 | c0019 | t0001 | g0091 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02145 | hp1 | a0017 | c0038 | t0001 | g0180 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02145 | hp2 | a0003 | c0008 | t0004 | g0122 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02257 | hp1 | a0018 | c0037 | t0001 | g0126 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02258 | hp2 | a0001 | c0031 | t0001 | g0260 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0040 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02293 | hp1 | a0004 | c0005 | t0002 | g0003 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02300 | hp2 | a0004 | c0005 | t0002 | g0003 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02451 | hp1 | a0001 | c0025 | t0002 | g0093 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02451 | hp2 | a0003 | c0008 | t0004 | g0081 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02572 | hp1 | a0001 | c0009 | t0002 | g0095 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02572 | hp2 | a0002 | c0011 | t0001 | g0167 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02602 | hp1 | a0005 | c0007 | t0001 | g0267 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0046 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02615 | hp1 | a0002 | c0011 | t0001 | g0166 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0042 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02622 | hp1 | a0012 | c0016 | t0001 | g0070 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02622 | hp2 | a0003 | c0004 | t0003 | g0176 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02630 | hp1 | a0007 | c0012 | t0003 | g0175 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02630 | hp2 | a0003 | c0008 | t0004 | g0246 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02683 | hp1 | a0005 | c0007 | t0001 | g0090 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02717 | hp1 | a0002 | c0011 | t0001 | g0066 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02717 | hp2 | a0003 | c0004 | t0003 | g0268 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02723 | hp2 | a0001 | c0006 | t0002 | g0038 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02818 | hp2 | a0007 | c0012 | t0003 | g0068 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02886 | hp2 | a0001 | c0014 | t0001 | g0262 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02896 | hp1 | a0013 | c0022 | t0002 | g0124 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02896 | hp2 | a0008 | c0013 | t0002 | g0005 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02897 | hp1 | a0008 | c0013 | t0002 | g0005 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02897 | hp2 | a0002 | c0011 | t0001 | g0059 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02922 | hp1 | a0001 | c0009 | t0002 | g0132 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02922 | hp2 | a0006 | c0010 | t0002 | g0013 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03041 | hp1 | a0003 | c0004 | t0003 | g0165 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03041 | hp2 | a0003 | c0004 | t0003 | g0189 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03098 | hp1 | a0006 | c0010 | t0002 | g0011 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03098 | hp2 | a0001 | c0009 | t0002 | g0094 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03130 | hp1 | a0001 | c0006 | t0002 | g0009 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03130 | hp2 | a0006 | c0010 | t0002 | g0271 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03139 | hp1 | a0001 | c0006 | t0002 | g0020 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0041 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03209 | hp1 | a0007 | c0012 | t0003 | g0083 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03209 | hp2 | a0001 | c0006 | t0002 | g0014 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03225 | hp2 | a0003 | c0004 | t0003 | g0249 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0016 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03486 | hp1 | a0003 | c0008 | t0004 | g0177 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03486 | hp2 | a0008 | c0013 | t0002 | g0183 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0050 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03516 | hp2 | a0003 | c0004 | t0003 | g0027 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03579 | hp1 | a0012 | c0016 | t0001 | g0088 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03710 | hp2 | a0019 | c0028 | t0001 | g0130 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04115 | hp2 | a0001 | c0034 | t0001 | g0121 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04184 | hp1 | a0005 | c0007 | t0001 | g0129 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0032 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18522 | hp1 | a0001 | c0006 | t0002 | g0010 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18906 | hp1 | a0003 | c0008 | t0004 | g0082 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18906 | hp2 | a0020 | c0032 | t0001 | g0168 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18946 | hp2 | a0001 | c0018 | t0001 | g0114 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18967 | hp2 | a0001 | c0003 | t0008 | g0051 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18983 | hp2 | a0001 | c0033 | t0010 | g0106 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18984 | hp1 | a0001 | c0018 | t0001 | g0113 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19000 | hp1 | a0001 | c0003 | t0002 | g0018 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19011 | hp2 | a0021 | c0035 | t0001 | g0242 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19030 | hp2 | a0001 | c0006 | t0002 | g0058 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19043 | hp1 | a0001 | c0003 | t0002 | g0048 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19043 | hp2 | a0011 | c0017 | t0001 | g0104 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19066 | hp2 | a0022 | c0026 | t0001 | g0097 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19240 | hp1 | a0003 | c0020 | t0006 | g0248 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA19240 | hp2 | a0003 | c0008 | t0005 | g0069 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20129 | hp1 | a0001 | c0014 | t0001 | g0145 | AFR | ASW | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0047 | AFR | ASW | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20752 | hp1 | a0005 | c0007 | t0001 | g0251 | EUR | TSI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20752 | hp2 | a0001 | c0023 | t0001 | g0230 | EUR | TSI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | GIH | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20905 | hp2 | a0005 | c0007 | t0001 | g0128 | SAS | GIH | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0057 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02486 | hp1 | a0011 | c0017 | t0001 | g0149 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02486 | hp2 | a0001 | c0006 | t0002 | g0022 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0021 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| HG06807 | hp2 | a0001 | c0009 | t0002 | g0182 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0049 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA20300 | hp2 | a0013 | c0021 | t0002 | g0250 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| NA21309 | hp2 | a0023 | c0024 | t0002 | g0026 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0009 | g0023 | REF | REF | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:581591 | C | T | 1 | a0017 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.79C>T | p.Pro27Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/18 | 223/5539 | 79/4950 | 27/1649 | chr11 | 581591 | |||
| chr11:581973 | G | C | 1 | a0009 | 2 | HG01256.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.106G>C | p.Val36Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/18 | 250/5539 | 106/4950 | 36/1649 | chr11 | 581973 | |||
| chr11:587372 | A | G | 1 | a0010 | 2 | HG02040.hp1 HG02083.hp1 |
missense_variant | MODERATE | c.328A>G | p.Ile110Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/18 | 472/5539 | 328/4950 | 110/1649 | chr11 | 587372 | |||
| chr11:597398 | C | T | 1 | a0018 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.722C>T | p.Ala241Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/18 | 866/5539 | 722/4950 | 241/1649 | chr11 | 597398 | |||
| chr11:598481 | G | T | 1 | a0015 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1003G>T | p.Ala335Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/18 | 1147/5539 | 1003/4950 | 335/1649 | chr11 | 598481 | |||
| chr11:607068 | C | T | 1 | a0021 | 1 | NA19011.hp2 | missense_variant&splice_region_variant | MODERATE | c.1612C>T | p.Pro538Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 1756/5539 | 1612/4950 | 538/1649 | chr11 | 607068 | |||
| chr11:607356 | G | A | 1 | a0007 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.1900G>A | p.Gly634Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2044/5539 | 1900/4950 | 634/1649 | chr11 | 607356 | |||
| chr11:607680 | G | A | 1 | a0022 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2224G>A | p.Gly742Arg | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2368/5539 | 2224/4950 | 742/1649 | chr11 | 607680 | |||
| chr11:607819 | C | A | 1 | a0008 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.2363C>A | p.Ser788Tyr | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2507/5539 | 2363/4950 | 788/1649 | chr11 | 607819 | |||
| chr11:607933 | G | A | 1 | a0023 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2477G>A | p.Arg826Gln | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2621/5539 | 2477/4950 | 826/1649 | chr11 | 607933 | |||
| chr11:608184 | G | T | 1 | a0013 | 2 | HG02896.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.2728G>T | p.Ala910Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2872/5539 | 2728/4950 | 910/1649 | chr11 | 608184 | |||
| chr11:608502 | CGGACGCG others(5): Show |
C | 3 | a0003 a0007 a0013 |
24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
disruptive_inframe_deletion | MODERATE | c.3059_3070delGGACGC others(6): Show |
p.Gly1020_Ser1023del | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3203/5539 | 3059/4950 | 1020/1649 | INFO_REALIGN_3_PRIME | chr11 | 608502 | ||
| chr11:608593 | G | A | 5 | a0005 a0010 a0016 others(2): Show |
13 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
missense_variant | MODERATE | c.3137G>A | p.Arg1046Gln | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3281/5539 | 3137/4950 | 1046/1649 | chr11 | 608593 | |||
| chr11:608871 | C | T | 1 | a0011 | 2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.3415C>T | p.Arg1139Trp | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3559/5539 | 3415/4950 | 1139/1649 | chr11 | 608871 | |||
| chr11:608959 | C | T | 1 | a0006 | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.3503C>T | p.Ser1168Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3647/5539 | 3503/4950 | 1168/1649 | chr11 | 608959 | |||
| chr11:609019 | G | C | 1 | a0014 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.3563G>C | p.Arg1188Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3707/5539 | 3563/4950 | 1188/1649 | chr11 | 609019 | |||
| chr11:609081 | G | C | 2 | a0012 a0018 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.3625G>C | p.Gly1209Arg | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3769/5539 | 3625/4950 | 1209/1649 | chr11 | 609081 | |||
| chr11:609145 | C | T | 1 | a0013 | 2 | HG02896.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.3689C>T | p.Pro1230Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3833/5539 | 3689/4950 | 1230/1649 | chr11 | 609145 | |||
| chr11:609148 | A | C | 1 | a0003 | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
missense_variant | MODERATE | c.3692A>C | p.Glu1231Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3836/5539 | 3692/4950 | 1231/1649 | chr11 | 609148 | |||
| chr11:609577 | C | T | 3 | a0003 a0007 a0013 |
24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
missense_variant | MODERATE | c.4121C>T | p.Ala1374Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4265/5539 | 4121/4950 | 1374/1649 | chr11 | 609577 | |||
| chr11:610277 | T | C | 15 | a0001 a0003 a0004 others(12): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
missense_variant | MODERATE | c.4346T>C | p.Val1449Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 15/18 | 4490/5539 | 4346/4950 | 1449/1649 | chr11 | 610277 | |||
| chr11:610724 | C | T | 1 | a0004 | 10 | HG00099.hp1 HG01175.hp1 HG01257.hp2 others(7): Show |
missense_variant | MODERATE | c.4640C>T | p.Ala1547Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 16/18 | 4784/5539 | 4640/4950 | 1547/1649 | chr11 | 610724 | |||
| chr11:611740 | C | T | 1 | a0003 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.4913C>T | p.Ala1638Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 5057/5539 | 4913/4950 | 1638/1649 | chr11 | 611740 | |||
| chr11:611752 | C | T | 2 | a0019 a0020 |
2 | HG03710.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.4925C>T | p.Pro1642Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 5069/5539 | 4925/4950 | 1642/1649 | chr11 | 611752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:581587 | G | A | 5 | a0003c0008 a0003c0020 a0007c0012 others(2): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.75G>A | p.Ala25Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/18 | 219/5539 | 75/4950 | 25/1649 | chr11 | 581587 | |||
| chr11:582056 | G | A | 1 | a0001c0023 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.189G>A | p.Glu63Glu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/18 | 333/5539 | 189/4950 | 63/1649 | chr11 | 582056 | |||
| chr11:587425 | C | A | 5 | a0001c0003 a0001c0006 a0004c0005 others(2): Show |
52 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(49): Show |
synonymous_variant | LOW | c.381C>A | p.Ala127Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/18 | 525/5539 | 381/4950 | 127/1649 | chr11 | 587425 | |||
| chr11:587452 | C | T | 1 | a0002c0011 | 4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.408C>T | p.Val136Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/18 | 552/5539 | 408/4950 | 136/1649 | chr11 | 587452 | |||
| chr11:592666 | C | T | 2 | a0013c0021 a0013c0022 |
2 | HG02896.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.612C>T | p.Cys204Cys | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/18 | 756/5539 | 612/4950 | 204/1649 | chr11 | 592666 | |||
| chr11:605277 | T | C | 5 | a0003c0008 a0003c0020 a0007c0012 others(2): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.1311T>C | p.Pro437Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 11/18 | 1455/5539 | 1311/4950 | 437/1649 | chr11 | 605277 | |||
| chr11:607175 | G | A | 4 | a0001c0003 a0001c0025 a0004c0005 others(1): Show |
40 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(37): Show |
synonymous_variant | LOW | c.1719G>A | p.Pro573Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 1863/5539 | 1719/4950 | 573/1649 | chr11 | 607175 | |||
| chr11:607649 | C | T | 1 | a0001c0018 | 2 | NA18946.hp2 NA18984.hp1 |
synonymous_variant | LOW | c.2193C>T | p.Ser731Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2337/5539 | 2193/4950 | 731/1649 | chr11 | 607649 | |||
| chr11:608180 | A | G | 1 | a0003c0008 | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
synonymous_variant | LOW | c.2724A>G | p.Ala908Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2868/5539 | 2724/4950 | 908/1649 | chr11 | 608180 | |||
| chr11:608333 | G | A | 1 | a0001c0027 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2877G>A | p.Thr959Thr | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3021/5539 | 2877/4950 | 959/1649 | chr11 | 608333 | |||
| chr11:608378 | G | A | 1 | a0013c0021 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.2922G>A | p.Pro974Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3066/5539 | 2922/4950 | 974/1649 | chr11 | 608378 | |||
| chr11:609068 | G | A | 8 | a0001c0003 a0001c0006 a0001c0009 others(5): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
synonymous_variant | LOW | c.3612G>A | p.Ala1204Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3756/5539 | 3612/4950 | 1204/1649 | chr11 | 609068 | |||
| chr11:609242 | C | T | 1 | a0001c0034 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.3786C>T | p.Gly1262Gly | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3930/5539 | 3786/4950 | 1262/1649 | chr11 | 609242 | |||
| chr11:609347 | T | G | 2 | a0013c0021 a0013c0022 |
2 | HG02896.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.3891T>G | p.Ser1297Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4035/5539 | 3891/4950 | 1297/1649 | chr11 | 609347 | |||
| chr11:609353 | G | A | 8 | a0001c0003 a0001c0006 a0001c0009 others(5): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
synonymous_variant | LOW | c.3897G>A | p.Pro1299Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4041/5539 | 3897/4950 | 1299/1649 | chr11 | 609353 | |||
| chr11:609521 | T | C | 2 | a0001c0014 a0001c0031 |
4 | HG01943.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.4065T>C | p.Ala1355Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4209/5539 | 4065/4950 | 1355/1649 | chr11 | 609521 | |||
| chr11:609701 | C | T | 1 | a0001c0031 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.4245C>T | p.Pro1415Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4389/5539 | 4245/4950 | 1415/1649 | chr11 | 609701 | |||
| chr11:610680 | C | T | 1 | a0001c0033 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.4596C>T | p.Ala1532Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 16/18 | 4740/5539 | 4596/4950 | 1532/1649 | chr11 | 610680 | |||
| chr11:611052 | C | T | 2 | a0016c0029 a0017c0038 |
2 | HG01243.hp2 HG02145.hp1 |
synonymous_variant | LOW | c.4776C>T | p.Tyr1592Tyr | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/18 | 4920/5539 | 4776/4950 | 1592/1649 | chr11 | 611052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:576517 | C | T | 1 | a0001c0033t0010 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/18 | 4996 | chr11 | 576517 | ||||||
| chr11:611796 | TATGCCCG others(71): Show |
T | 1 | a0003c0008t0005 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51_*128delTCGGGGC others(71): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 51 | INFO_REALIGN_3_PRIME | chr11 | 611796 | |||||
| chr11:611802 | C | G | 1 | a0001c0003t0002 | 4 | HG00639.hp1 HG00741.hp2 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*25C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 25 | chr11 | 611802 | ||||||
| chr11:611814 | G | C | 1 | a0003c0020t0006 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 37 | chr11 | 611814 | ||||||
| chr11:611830 | G | A | 1 | a0001c0001t0001 | 4 | HG00408.hp2 NA18947.hp2 NA18984.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*53G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 53 | chr11 | 611830 | ||||||
| chr11:611841 | C | T | 1 | a0001c0003t0002 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 64 | chr11 | 611841 | ||||||
| chr11:611868 | C | T | 12 | a0001c0003t0002 a0001c0003t0008 a0001c0006t0002 others(9): Show |
67 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 91 | chr11 | 611868 | ||||||
| chr11:611869 | G | A | 1 | a0001c0001t0001 | 2 | HG00597.hp2 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*92G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 92 | chr11 | 611869 | ||||||
| chr11:611919 | C | G | 17 | a0001c0003t0002 a0001c0003t0008 a0001c0006t0002 others(14): Show |
85 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*142C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 142 | chr11 | 611919 | ||||||
| chr11:611923 | G | A | 1 | a0003c0020t0006 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 146 | chr11 | 611923 | ||||||
| chr11:611982 | A | G | 1 | a0001c0003t0008 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 205 | chr11 | 611982 | ||||||
| chr11:612145 | C | G | 1 | a0001c0009t0007 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*368C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 368 | chr11 | 612145 | ||||||
| chr11:612148 | T | C | 15 | a0001c0003t0002 a0001c0003t0008 a0001c0006t0002 others(12): Show |
70 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*371T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 371 | chr11 | 612148 | ||||||
| chr11:612176 | G | A | 2 | a0003c0008t0004 a0003c0008t0005 |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*399G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 399 | chr11 | 612176 | ||||||
| chr11:612182 | T | C | 17 | a0001c0003t0002 a0001c0003t0008 a0001c0006t0002 others(14): Show |
85 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*405T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 405 | chr11 | 612182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:576634 | C | T | 1 | a0006c0010t0002g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-22+42C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576634 | |||||||
| chr11:576665 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-22+73G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576665 | |||||||
| chr11:576683 | ACCGCGGG others(12): Show |
A | 1 | a0001c0001t0001g0008 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-22+97_-22+115delG others(18): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576683 | ||||||
| chr11:576745 | G | GCTGGGAG others(12): Show |
17 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(14): Show |
18 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22+317_-22+335dup others(19): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | G | GCTGGGAG others(31): Show |
7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
7 | HG00438.hp2 HG01981.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22+298_-22+335dup others(38): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | G | GCTGGGAG others(69): Show |
1 | a0002c0011t0001g0059 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-22+260_-22+335dup others(76): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | GCTGGGAG others(12): Show |
G | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0131 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-22+317_-22+335del others(19): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | GCTGGGAG others(31): Show |
G | 48 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(45): Show |
51 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-22+298_-22+335del others(38): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | GCTGGGAG others(50): Show |
G | 39 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(36): Show |
39 | HG00280.hp1 HG00558.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.-22+279_-22+335del others(57): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | GCTGGGAG others(69): Show |
G | 22 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22+260_-22+335del others(76): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | GCTGGGAG others(88): Show |
G | 9 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0003t0002g0018 others(6): Show |
9 | HG01952.hp2 HG01981.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+241_-22+335del others(95): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576745 | GCTGGGAG others(107): Show |
G | 36 | a0001c0003t0002g0024 a0001c0003t0002g0028 a0001c0003t0002g0029 others(33): Show |
37 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-22+222_-22+335del | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | ||||||
| chr11:576768 | G | A | 2 | a0001c0006t0002g0009 a0001c0006t0002g0010 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-22+176G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576768 | |||||||
| chr11:576806 | G | A | 6 | a0001c0003t0002g0015 a0001c0006t0002g0014 a0006c0010t0002g0011 others(3): Show |
6 | HG01192.hp2 HG01891.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+214G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576806 | |||||||
| chr11:576825 | G | A | 2 | a0001c0003t0002g0016 a0001c0006t0002g0017 |
2 | HG01192.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-22+233G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576825 | |||||||
| chr11:576844 | G | A | 5 | a0001c0003t0002g0018 a0001c0003t0002g0021 a0001c0006t0002g0020 others(2): Show |
5 | HG01981.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+252G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576844 | |||||||
| chr11:576863 | G | A | 36 | a0001c0003t0002g0024 a0001c0003t0002g0028 a0001c0003t0002g0029 others(33): Show |
37 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-22+271G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576863 | |||||||
| chr11:576871 | C | G | 1 | a0001c0006t0002g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22+279C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576871 | |||||||
| chr11:577167 | T | G | 1 | a0020c0032t0001g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22+575T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577167 | |||||||
| chr11:577180 | C | G | 4 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+588C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577180 | |||||||
| chr11:577238 | C | T | 4 | a0002c0011t0001g0059 a0002c0011t0001g0066 a0002c0011t0001g0166 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+646C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577238 | |||||||
| chr11:577269 | A | G | 1 | a0001c0003t0002g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-22+677A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577269 | |||||||
| chr11:577296 | G | C | 11 | a0002c0002t0001g0002 a0002c0002t0001g0067 a0002c0002t0001g0123 others(8): Show |
13 | HG00597.hp1 HG00609.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22+704G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577296 | |||||||
| chr11:577309 | G | A | 18 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+717G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577309 | |||||||
| chr11:577330 | C | T | 1 | a0003c0004t0003g0165 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-22+738C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577330 | |||||||
| chr11:577354 | T | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(13): Show |
17 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+762T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577354 | |||||||
| chr11:577442 | C | T | 18 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+850C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577442 | |||||||
| chr11:577454 | C | T | 16 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(13): Show |
17 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+862C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577454 | |||||||
| chr11:577534 | G | A | 70 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(67): Show |
72 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-22+942G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577534 | |||||||
| chr11:577670 | C | G | 16 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(13): Show |
17 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+1078C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577670 | |||||||
| chr11:577684 | G | A | 18 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1092G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577684 | |||||||
| chr11:577696 | A | T | 1 | a0002c0002t0001g0266 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-22+1104A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577696 | |||||||
| chr11:577727 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-22+1135C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577727 | |||||||
| chr11:577735 | C | T | 1 | a0002c0002t0001g0245 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-22+1143C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577735 | |||||||
| chr11:577809 | C | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(68): Show |
71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22+1217C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577809 | |||||||
| chr11:577903 | T | G | 18 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1311T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577903 | |||||||
| chr11:577908 | G | C | 18 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1316G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577908 | |||||||
| chr11:577915 | T | C | 18 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1323T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577915 | |||||||
| chr11:578078 | G | T | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+1486G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578078 | |||||||
| chr11:578222 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-22+1630G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578222 | |||||||
| chr11:578230 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-22+1638G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578230 | |||||||
| chr11:578294 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-22+1702C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578294 | |||||||
| chr11:578759 | A | G | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(106): Show |
110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22+2167A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578759 | |||||||
| chr11:578844 | C | G | 52 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-22+2252C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578844 | |||||||
| chr11:578954 | A | G | 1 | a0002c0002t0001g0141 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-22+2362A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578954 | |||||||
| chr11:578976 | A | G | 20 | a0002c0002t0001g0001 a0002c0002t0001g0060 a0002c0002t0001g0099 others(17): Show |
22 | HG00558.hp1 HG00673.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+2384A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578976 | |||||||
| chr11:578996 | T | C | 197 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(194): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-22+2404T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578996 | |||||||
| chr11:579048 | T | C | 1 | a0003c0004t0003g0006 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-21-2444T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579048 | |||||||
| chr11:579049 | A | T | 1 | a0003c0004t0003g0006 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-21-2443A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579049 | |||||||
| chr11:579078 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-21-2414C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579078 | |||||||
| chr11:579188 | G | C | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21-2304G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579188 | |||||||
| chr11:579220 | T | TCCCCCAG others(11): Show |
3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-21-2238_-21-2221d others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579220 | ||||||
| chr11:579220 | TCCCCCAG others(11): Show |
T | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-21-2238_-21-2221d others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579220 | ||||||
| chr11:579253 | C | T | 1 | a0001c0006t0002g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-21-2239C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579253 | |||||||
| chr11:579254 | C | CTCCCCCC others(11): Show |
66 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(63): Show |
68 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-21-2222_-21-2221i others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579254 | ||||||
| chr11:579254 | C | T | 1 | a0001c0006t0002g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-21-2238C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579254 | |||||||
| chr11:579256 | C | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(31): Show |
34 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-21-2236C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579256 | |||||||
| chr11:579354 | C | T | 13 | a0005c0007t0001g0090 a0005c0007t0001g0128 a0005c0007t0001g0129 others(10): Show |
13 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-2138C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579354 | |||||||
| chr11:579412 | T | C | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21-2080T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579412 | |||||||
| chr11:579417 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-21-2075C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579417 | |||||||
| chr11:579421 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-21-2071C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579421 | |||||||
| chr11:579467 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21-2025G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579467 | |||||||
| chr11:579546 | C | T | 6 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(3): Show |
7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-1946C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579546 | |||||||
| chr11:579568 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1924C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579568 | |||||||
| chr11:579596 | G | A | 4 | a0006c0010t0002g0011 a0006c0010t0002g0012 a0006c0010t0002g0013 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1896G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579596 | |||||||
| chr11:579608 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-21-1884G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579608 | |||||||
| chr11:579676 | C | T | 6 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(3): Show |
7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-1816C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579676 | |||||||
| chr11:579718 | G | GAAGAAAG others(370): Show |
1 | a0001c0001t0001g0200 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-21-1757_-21-1756i others(379): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579718 | ||||||
| chr11:579736 | A | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0263 a0001c0001t0001g0269 others(1): Show |
4 | HG01928.hp1 HG01952.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1756A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579736 | |||||||
| chr11:579757 | C | T | 1 | a0002c0002t0001g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-21-1735C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579757 | |||||||
| chr11:579768 | T | G | 1 | a0001c0006t0002g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-21-1724T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579768 | |||||||
| chr11:579823 | C | T | 2 | a0007c0012t0003g0083 a0007c0012t0003g0175 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-21-1669C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579823 | |||||||
| chr11:579855 | G | T | 1 | a0001c0009t0007g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-21-1637G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579855 | |||||||
| chr11:579948 | C | T | 2 | a0001c0001t0001g0072 a0006c0010t0002g0013 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-21-1544C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579948 | |||||||
| chr11:580020 | T | C | 1 | a0014c0030t0001g0181 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-21-1472T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580020 | |||||||
| chr11:580166 | C | T | 2 | a0001c0003t0002g0055 a0001c0003t0002g0056 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-21-1326C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580166 | |||||||
| chr11:580199 | G | A | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-21-1293G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580199 | |||||||
| chr11:580290 | C | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1202C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580290 | |||||||
| chr11:580309 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1183G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580309 | |||||||
| chr11:580349 | T | C | 1 | a0002c0002t0001g0247 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-21-1143T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580349 | |||||||
| chr11:580402 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1090C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580402 | |||||||
| chr11:580480 | G | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1012G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580480 | |||||||
| chr11:580501 | A | C | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-21-991A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580501 | |||||||
| chr11:580668 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0265 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-21-824T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580668 | |||||||
| chr11:580732 | A | G | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-760A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580732 | |||||||
| chr11:580770 | C | T | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-722C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580770 | |||||||
| chr11:580911 | A | G | 1 | a0002c0002t0001g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-21-581A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580911 | |||||||
| chr11:580969 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-523G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580969 | |||||||
| chr11:581051 | C | T | 1 | a0001c0003t0002g0054 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-21-441C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581051 | |||||||
| chr11:581092 | G | A | 10 | a0001c0001t0001g0092 a0001c0001t0001g0131 a0001c0009t0002g0094 others(7): Show |
11 | HG01074.hp1 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-400G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581092 | |||||||
| chr11:581111 | AT | A | 19 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0227 others(16): Show |
19 | HG01257.hp2 HG02015.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.-21-365delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 581111 | ||||||
| chr11:581189 | G | A | 4 | a0006c0010t0002g0011 a0006c0010t0002g0012 a0006c0010t0002g0013 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-303G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581189 | |||||||
| chr11:581235 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-21-257G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581235 | |||||||
| chr11:581256 | T | TAGGGCTC others(94): Show |
6 | a0003c0020t0006g0248 a0007c0012t0003g0068 a0007c0012t0003g0083 others(3): Show |
6 | HG02630.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-226_-21-126dup others(101): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 581256 | ||||||
| chr11:581256 | T | TAGGGCTC others(94): Show |
6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-203_-21-202ins others(101): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 581256 | ||||||
| chr11:581455 | G | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-21-37G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581455 | |||||||
| chr11:581769 | A | G | 2 | a0001c0006t0002g0009 a0001c0006t0002g0010 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.94+163A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/17 | chr11 | 581769 | |||||||
| chr11:581773 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.94+167C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/17 | chr11 | 581773 | |||||||
| chr11:581803 | T | C | 7 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(4): Show |
8 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-159T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/17 | chr11 | 581803 | |||||||
| chr11:582107 | C | G | 2 | a0002c0002t0001g0224 a0002c0002t0001g0225 |
2 | NA18941.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.214+26C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582107 | |||||||
| chr11:582126 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.214+45C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582126 | |||||||
| chr11:582264 | C | CT | 11 | a0001c0001t0001g0072 a0002c0002t0001g0173 a0003c0008t0004g0081 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+201dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 582264 | ||||||
| chr11:582264 | CT | C | 175 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(172): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.214+201delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 582264 | ||||||
| chr11:582504 | C | T | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.214+423C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582504 | |||||||
| chr11:582587 | C | T | 1 | a0001c0006t0002g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214+506C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582587 | |||||||
| chr11:582727 | C | T | 51 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.214+646C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582727 | |||||||
| chr11:582803 | C | T | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+722C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582803 | |||||||
| chr11:582815 | C | T | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214+734C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582815 | |||||||
| chr11:582819 | C | T | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214+738C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582819 | |||||||
| chr11:582927 | G | A | 8 | a0005c0007t0001g0090 a0005c0007t0001g0128 a0005c0007t0001g0129 others(5): Show |
8 | HG01168.hp2 HG02040.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+846G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582927 | |||||||
| chr11:583050 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.214+969A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583050 | |||||||
| chr11:583053 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.214+972C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583053 | |||||||
| chr11:583078 | C | A | 1 | a0001c0003t0002g0028 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.214+997C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583078 | |||||||
| chr11:583083 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.214+1002G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583083 | |||||||
| chr11:583107 | G | A | 29 | a0001c0003t0002g0018 a0001c0003t0002g0024 a0001c0003t0002g0028 others(26): Show |
31 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.214+1026G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583107 | |||||||
| chr11:583111 | C | T | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+1030C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583111 | |||||||
| chr11:583122 | G | C | 17 | a0001c0003t0002g0029 a0001c0003t0002g0030 a0001c0003t0002g0031 others(14): Show |
18 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+1041G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583122 | |||||||
| chr11:583145 | T | C | 8 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0011t0001g0059 others(5): Show |
8 | HG01975.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1064T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583145 | |||||||
| chr11:583146 | G | C | 8 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0011t0001g0059 others(5): Show |
8 | HG01975.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1065G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583146 | |||||||
| chr11:583147 | T | C | 7 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0011t0001g0059 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+1066T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583147 | |||||||
| chr11:583156 | T | C | 21 | a0001c0003t0002g0021 a0001c0003t0002g0029 a0001c0003t0002g0030 others(18): Show |
21 | HG00140.hp1 HG01123.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.214+1075T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583156 | |||||||
| chr11:583158 | G | A | 21 | a0001c0003t0002g0021 a0001c0003t0002g0029 a0001c0003t0002g0030 others(18): Show |
21 | HG00140.hp1 HG01123.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.214+1077G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583158 | |||||||
| chr11:583168 | G | A | 3 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0014c0030t0001g0181 |
3 | HG00544.hp2 NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.214+1087G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583168 | |||||||
| chr11:583223 | C | T | 1 | a0003c0004t0003g0006 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.214+1142C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583223 | |||||||
| chr11:583270 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG00544.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.214+1189C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583270 | |||||||
| chr11:583327 | ACT | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0018t0001g0113 others(1): Show |
4 | HG00438.hp2 NA18946.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1249_214+1250d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 583327 | ||||||
| chr11:583350 | A | G | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.214+1269A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583350 | |||||||
| chr11:583404 | C | T | 3 | a0003c0004t0003g0189 a0003c0004t0003g0221 a0003c0004t0003g0268 |
3 | HG01346.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.214+1323C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583404 | |||||||
| chr11:583590 | A | G | 2 | a0001c0003t0002g0037 a0023c0024t0002g0026 |
2 | HG00639.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.214+1509A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583590 | |||||||
| chr11:583612 | G | A | 3 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0003c0004t0003g0165 |
3 | HG02559.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214+1531G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583612 | |||||||
| chr11:583731 | TCAAA | T | 51 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.214+1655_214+1658d others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 583731 | ||||||
| chr11:583747 | G | A | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.214+1666G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583747 | |||||||
| chr11:583767 | C | T | 51 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.214+1686C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583767 | |||||||
| chr11:583787 | T | C | 63 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(60): Show |
64 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.214+1706T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583787 | |||||||
| chr11:584010 | C | T | 1 | a0002c0002t0001g0220 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.214+1929C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584010 | |||||||
| chr11:584099 | A | G | 1 | a0002c0002t0001g0173 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.214+2018A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584099 | |||||||
| chr11:584112 | G | A | 104 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.214+2031G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584112 | |||||||
| chr11:584243 | C | T | 47 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.214+2162C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584243 | |||||||
| chr11:584371 | C | T | 1 | a0003c0008t0004g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214+2290C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584371 | |||||||
| chr11:584395 | C | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+2314C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584395 | |||||||
| chr11:584479 | G | A | 1 | a0004c0005t0002g0043 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.214+2398G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584479 | |||||||
| chr11:584514 | G | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0018t0001g0113 others(1): Show |
4 | HG00438.hp2 NA18946.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2433G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584514 | |||||||
| chr11:584516 | G | A | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.214+2435G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584516 | |||||||
| chr11:584572 | G | A | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.214+2491G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584572 | |||||||
| chr11:584591 | A | G | 70 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(67): Show |
72 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.214+2510A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584591 | |||||||
| chr11:584594 | G | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+2513G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584594 | |||||||
| chr11:584724 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.215-2535A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584724 | |||||||
| chr11:584729 | C | CT | 33 | a0001c0001t0001g0062 a0001c0001t0001g0103 a0001c0001t0001g0115 others(30): Show |
34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.215-2505dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 584729 | ||||||
| chr11:584729 | C | CTT | 11 | a0001c0001t0001g0150 a0002c0002t0001g0086 a0002c0002t0001g0087 others(8): Show |
11 | HG00673.hp2 HG01433.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-2506_215-2505d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 584729 | ||||||
| chr11:584729 | C | G | 1 | a0020c0032t0001g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.215-2530C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584729 | |||||||
| chr11:584729 | CT | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0160 a0001c0001t0001g0196 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-2505delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 584729 | ||||||
| chr11:584736 | T | G | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2523T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584736 | |||||||
| chr11:584767 | C | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0263 a0001c0001t0001g0269 others(1): Show |
4 | HG01928.hp1 HG01952.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-2492C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584767 | |||||||
| chr11:584769 | C | T | 7 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(4): Show |
8 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2490C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584769 | |||||||
| chr11:584790 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0228 |
2 | HG01106.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.215-2469T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584790 | |||||||
| chr11:584791 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2468G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584791 | |||||||
| chr11:584792 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2467T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584792 | |||||||
| chr11:584846 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2413T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584846 | |||||||
| chr11:584931 | T | C | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-2328T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584931 | |||||||
| chr11:585014 | A | T | 1 | a0018c0037t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-2245A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585014 | |||||||
| chr11:585026 | C | A | 1 | a0001c0033t0010g0106 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.215-2233C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585026 | |||||||
| chr11:585043 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2216T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585043 | |||||||
| chr11:585175 | C | T | 2 | a0005c0007t0001g0251 a0005c0007t0001g0252 |
2 | HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.215-2084C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585175 | |||||||
| chr11:585208 | T | TGCCCTTT others(775): Show |
1 | a0001c0001t0001g0256 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.215-1865_215-1864i others(784): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | ||||||
| chr11:585208 | T | TGCCCTTT others(821): Show |
5 | a0002c0002t0001g0073 a0002c0002t0001g0105 a0002c0002t0001g0254 others(2): Show |
6 | HG01069.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1865_215-1864i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | ||||||
| chr11:585208 | T | TGCCCTTT others(338): Show |
1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-2003_215-2002i others(347): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | ||||||
| chr11:585208 | T | TGCCCTTT others(223): Show |
3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-2003_215-2002i others(232): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | ||||||
| chr11:585208 | TGCCCTTT others(108): Show |
T | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.215-1864_215-1750d others(2): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | ||||||
| chr11:585211 | C | CCTTTCCA others(1396): Show |
1 | a0001c0006t0002g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1405): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585211 | ||||||
| chr11:585211 | C | CCTTTCCA others(1718): Show |
1 | a0001c0003t0002g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585211 | ||||||
| chr11:585221 | T | TTGAGGTA others(775): Show |
1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(784): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585221 | ||||||
| chr11:585221 | T | TTGAGGTA others(292): Show |
1 | a0003c0008t0004g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.215-2003_215-2002i others(301): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585221 | ||||||
| chr11:585234 | C | CCTTTCCA others(39): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02132.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.215-2016_215-2015i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1718): Show |
1 | a0001c0006t0002g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-1842_215-1841i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1718): Show |
3 | a0001c0003t0002g0016 a0001c0006t0002g0009 a0001c0006t0002g0010 |
3 | HG03130.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1695): Show |
1 | a0001c0006t0002g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-1865_215-1864i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1741): Show |
1 | a0001c0003t0002g0024 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.215-1934_215-1933i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1741): Show |
1 | a0001c0003t0002g0018 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.215-1934_215-1933i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1741): Show |
1 | a0006c0010t0002g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1741): Show |
1 | a0006c0010t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1718): Show |
2 | a0001c0003t0002g0039 a0001c0003t0002g0040 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1695): Show |
3 | a0001c0003t0002g0041 a0001c0003t0002g0054 a0001c0006t0002g0058 |
3 | HG02280.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1718): Show |
1 | a0001c0003t0002g0031 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1718): Show |
1 | a0001c0003t0002g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1718): Show |
12 | a0001c0003t0002g0029 a0001c0003t0002g0030 a0001c0003t0002g0032 others(9): Show |
12 | HG01123.hp2 HG01255.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1695): Show |
1 | a0001c0003t0002g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1741): Show |
1 | a0001c0006t0002g0017 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(1695): Show |
1 | a0001c0003t0002g0053 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(292): Show |
4 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-2003_215-2002i others(301): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585234 | C | CCTTTCCA others(315): Show |
1 | a0003c0008t0005g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.215-2003_215-2002i others(324): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | ||||||
| chr11:585244 | T | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0107 |
2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.215-2015T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585244 | |||||||
| chr11:585257 | C | CCTTTCCA others(2017): Show |
1 | a0001c0006t0002g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-1842_215-1841i others(2026): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1672): Show |
1 | a0004c0005t0002g0044 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.215-1842_215-1841i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1672): Show |
2 | a0001c0003t0002g0028 a0001c0003t0002g0037 |
2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1672): Show |
1 | a0001c0003t0002g0045 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1603): Show |
1 | a0004c0005t0002g0033 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1612): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1649): Show |
1 | a0001c0003t0002g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1658): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(752): Show |
1 | a0023c0024t0002g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(761): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1672): Show |
1 | a0001c0003t0002g0015 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | CCTTTCCA others(1672): Show |
8 | a0001c0003t0002g0052 a0004c0005t0002g0003 a0004c0005t0002g0019 others(5): Show |
9 | HG00735.hp1 HG01175.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | ||||||
| chr11:585257 | C | T | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-2002C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585257 | |||||||
| chr11:585280 | C | CCTTTCCA others(16): Show |
1 | a0001c0006t0002g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585280 | ||||||
| chr11:585280 | C | CCTTTCCA others(1626): Show |
1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1635): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585280 | ||||||
| chr11:585280 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0107 |
2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.215-1979C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585280 | |||||||
| chr11:585290 | T | TTGAGGTA others(16): Show |
3 | a0001c0001t0001g0231 a0001c0001t0001g0263 a0001c0023t0001g0230 |
3 | HG01928.hp1 HG02300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.215-1947_215-1946i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585290 | ||||||
| chr11:585290 | T | TTGAGGTA others(200): Show |
2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-1947_215-1946i others(209): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585290 | ||||||
| chr11:585303 | C | T | 11 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(8): Show |
12 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1956C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585303 | |||||||
| chr11:585313 | T | A | 4 | a0001c0001t0001g0269 a0007c0012t0003g0068 a0007c0012t0003g0083 others(1): Show |
4 | HG01952.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1946T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585313 | |||||||
| chr11:585326 | C | T | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-1933C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585326 | |||||||
| chr11:585336 | T | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02132.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.215-1923T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585336 | |||||||
| chr11:585336 | T | TTGAGGTA others(39): Show |
2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-1888_215-1887i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585336 | ||||||
| chr11:585349 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0245 |
3 | HG02132.hp1 NA18943.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.215-1910C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585349 | |||||||
| chr11:585372 | C | CCTTTCCA others(2385): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0107 |
2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.215-1878_215-1877i others(2394): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585372 | ||||||
| chr11:585372 | C | T | 17 | a0001c0009t0002g0094 a0002c0002t0001g0060 a0002c0002t0001g0133 others(14): Show |
18 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.215-1887C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585372 | |||||||
| chr11:585382 | T | TTGAGGTA others(821): Show |
1 | a0002c0002t0001g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215-1865_215-1864i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585382 | ||||||
| chr11:585395 | C | CCTTTCCA others(16): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0212 |
2 | NA18946.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585395 | ||||||
| chr11:585395 | C | T | 66 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0131 others(63): Show |
69 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.215-1864C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585395 | |||||||
| chr11:585405 | T | A | 6 | a0001c0001t0001g0256 a0002c0002t0001g0073 a0002c0002t0001g0105 others(3): Show |
7 | HG01069.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-1854T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585405 | |||||||
| chr11:585405 | T | TTGAGGTA others(844): Show |
2 | a0001c0027t0001g0253 a0002c0002t0001g0184 |
2 | HG00099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | ||||||
| chr11:585405 | T | TTGAGGTA others(844): Show |
3 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0014c0030t0001g0181 |
3 | HG00544.hp2 NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | ||||||
| chr11:585405 | T | TTGAGGTA others(844): Show |
12 | a0002c0002t0001g0001 a0002c0002t0001g0099 a0002c0002t0001g0100 others(9): Show |
14 | HG01123.hp1 HG01256.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-1842_215-1841i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | ||||||
| chr11:585405 | T | TTGAGGTA others(821): Show |
8 | a0002c0002t0001g0135 a0002c0002t0001g0136 a0002c0002t0001g0188 others(5): Show |
8 | HG01943.hp1 HG02040.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1842_215-1841i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | ||||||
| chr11:585405 | T | TTGAGGTA others(798): Show |
1 | a0002c0002t0001g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-1842_215-1841i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | ||||||
| chr11:585418 | C | CCTTTCCA others(39): Show |
35 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0078 others(32): Show |
35 | HG00280.hp2 HG00673.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.215-1796_215-1795i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | ||||||
| chr11:585418 | C | CCTTTCCA others(4156): Show |
1 | a0002c0002t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.215-1796_215-1795i others(4165): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | ||||||
| chr11:585418 | C | CCTTTCCA others(4110): Show |
1 | a0002c0002t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.215-1796_215-1795i others(4119): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | ||||||
| chr11:585418 | C | CCTTTCCA others(4110): Show |
1 | a0003c0004t0003g0165 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-1796_215-1795i others(4119): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | ||||||
| chr11:585418 | C | CCTTTCCA others(16): Show |
32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(29): Show |
32 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.215-1819_215-1818i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | ||||||
| chr11:585418 | C | T | 32 | a0001c0001t0001g0074 a0001c0001t0001g0089 a0001c0001t0001g0107 others(29): Show |
35 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.215-1841C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585418 | |||||||
| chr11:585428 | T | A | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-1831T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585428 | |||||||
| chr11:585441 | C | CCTTTCCA others(39): Show |
4 | a0001c0001t0001g0160 a0001c0001t0001g0199 a0005c0007t0001g0251 others(1): Show |
4 | HG00438.hp1 HG02004.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1773_215-1772i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585441 | ||||||
| chr11:585441 | C | T | 12 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0060 others(9): Show |
12 | HG02080.hp2 HG02132.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-1818C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585441 | |||||||
| chr11:585451 | T | A | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-1808T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585451 | |||||||
| chr11:585464 | C | CCTTTCCA others(16): Show |
4 | a0003c0004t0003g0006 a0003c0004t0003g0085 a0003c0004t0003g0215 others(1): Show |
4 | HG01169.hp1 HG01433.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1786_215-1785i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585464 | ||||||
| chr11:585464 | C | CCTTTCCA others(16): Show |
2 | a0001c0018t0001g0113 a0001c0018t0001g0114 |
2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.215-1773_215-1772i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585464 | ||||||
| chr11:585464 | C | T | 28 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0102 others(25): Show |
29 | HG00140.hp2 HG00408.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.215-1795C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585464 | |||||||
| chr11:585474 | T | A | 56 | a0001c0001t0001g0074 a0001c0001t0001g0107 a0001c0003t0002g0015 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-1785T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585474 | |||||||
| chr11:585474 | T | ATGAGGTA others(16): Show |
4 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(1): Show |
4 | HG00639.hp2 HG01168.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1786_215-1785i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585474 | |||||||
| chr11:585474 | T | TTGAGGTA others(4685): Show |
1 | a0005c0007t0001g0178 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | ||||||
| chr11:585474 | T | TTGAGGTA others(4685): Show |
1 | a0005c0007t0001g0090 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | ||||||
| chr11:585474 | T | TTGAGGTA others(4708): Show |
1 | a0010c0019t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | ||||||
| chr11:585474 | T | TTGAGGTA others(4708): Show |
1 | a0010c0019t0001g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | ||||||
| chr11:585487 | C | CCTTTCCA others(2339): Show |
1 | a0001c0001t0001g0151 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.215-1763_215-1762i others(2348): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(2339): Show |
1 | a0001c0001t0001g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.215-1763_215-1762i others(2348): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(4793): Show |
1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4802): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(3098): Show |
1 | a0001c0001t0001g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(3107): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(4639): Show |
1 | a0005c0007t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(2868): Show |
1 | a0001c0001t0001g0265 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.215-1750_215-1749i others(2877): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(4823): Show |
1 | a0001c0001t0001g0209 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(2362): Show |
1 | a0001c0001t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(2371): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(936): Show |
1 | a0001c0001t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(945): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(4823): Show |
1 | a0001c0001t0001g0210 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(3144): Show |
1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(3153): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(4225): Show |
1 | a0012c0016t0001g0088 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4234): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(2523): Show |
1 | a0012c0016t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(2532): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(4892): Show |
1 | a0001c0001t0001g0231 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4901): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(39): Show |
2 | a0005c0007t0001g0128 a0005c0007t0001g0179 |
2 | HG02056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.215-1750_215-1749i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(3742): Show |
1 | a0017c0038t0001g0180 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.215-1694_215-1693i others(3751): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(3742): Show |
1 | a0016c0029t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.215-1694_215-1693i others(3751): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | CCTTTCCA others(1718): Show |
1 | a0001c0006t0002g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.215-1681_215-1680i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | ||||||
| chr11:585487 | C | T | 66 | a0001c0001t0001g0074 a0001c0001t0001g0107 a0001c0003t0002g0015 others(63): Show |
68 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-1772C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585487 | |||||||
| chr11:585497 | T | A | 10 | a0001c0006t0002g0038 a0001c0009t0002g0094 a0002c0002t0001g0060 others(7): Show |
10 | HG02080.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-1762T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585497 | |||||||
| chr11:585497 | T | TTGAGGTA others(16): Show |
3 | a0001c0001t0001g0163 a0003c0004t0003g0221 a0003c0004t0003g0268 |
3 | HG01346.hp1 HG02717.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.215-1750_215-1749i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585497 | ||||||
| chr11:585510 | T | C | 135 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(132): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.215-1749T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585510 | |||||||
| chr11:585511 | C | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0107 a0001c0001t0001g0151 others(1): Show |
4 | HG02132.hp1 NA18963.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1748C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585511 | |||||||
| chr11:585520 | T | A | 64 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0131 others(61): Show |
70 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.215-1739T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585520 | |||||||
| chr11:585520 | T | TTGAGGTA others(16): Show |
33 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(30): Show |
33 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.215-1717_215-1716i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585520 | ||||||
| chr11:585533 | C | T | 28 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0092 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.215-1726C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585533 | |||||||
| chr11:585534 | C | CTTTCCAG others(2224): Show |
1 | a0001c0001t0001g0201 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.215-1717_215-1716i others(2233): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585534 | ||||||
| chr11:585543 | T | A | 38 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.215-1716T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585543 | |||||||
| chr11:585543 | T | TTGAGGTA others(16): Show |
1 | a0001c0001t0001g0108 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.215-1694_215-1693i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585543 | ||||||
| chr11:585547 | G | A | 7 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(4): Show |
8 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-1712G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585547 | |||||||
| chr11:585556 | C | T | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-1703C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585556 | |||||||
| chr11:585566 | T | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0160 a0001c0001t0001g0199 others(35): Show |
41 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.215-1693T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585566 | |||||||
| chr11:585566 | T | TTGAGGTA others(16): Show |
8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0207 others(5): Show |
8 | HG00408.hp2 HG00609.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1671_215-1670i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585566 | ||||||
| chr11:585579 | C | CCTTTCCA others(4731): Show |
2 | a0001c0018t0001g0113 a0001c0018t0001g0114 |
2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.215-1671_215-1670i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585579 | ||||||
| chr11:585579 | C | CCTTTCCA others(2707): Show |
1 | a0001c0001t0001g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.215-1671_215-1670i others(2716): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585579 | ||||||
| chr11:585579 | C | CCTTTCCA others(637): Show |
1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-1658_215-1657i others(646): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585579 | ||||||
| chr11:585579 | C | T | 116 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0102 others(113): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.215-1680C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585579 | |||||||
| chr11:585589 | T | TTGAGGTA others(16): Show |
2 | a0005c0007t0001g0267 a0018c0037t0001g0126 |
2 | HG02257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.215-1648_215-1647i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585589 | ||||||
| chr11:585602 | C | CCTTTCCA others(729): Show |
1 | a0003c0008t0004g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.215-1585_215-1584i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | ||||||
| chr11:585602 | C | CCTTTCCA others(752): Show |
3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-1612_215-1611i others(761): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | ||||||
| chr11:585602 | C | CCTTTCCA others(729): Show |
2 | a0003c0008t0004g0177 a0003c0008t0005g0069 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-1635_215-1634i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | ||||||
| chr11:585602 | C | CCTTTCCA others(729): Show |
3 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 |
3 | HG02145.hp2 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.215-1635_215-1634i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | ||||||
| chr11:585602 | C | T | 9 | a0001c0001t0001g0201 a0003c0004t0003g0006 a0003c0004t0003g0027 others(6): Show |
10 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-1657C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585602 | |||||||
| chr11:585603 | C | T | 4 | a0001c0003t0002g0018 a0001c0003t0002g0024 a0001c0003t0002g0053 others(1): Show |
4 | HG01074.hp2 HG02015.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1656C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585603 | |||||||
| chr11:585612 | T | A | 2 | a0005c0007t0001g0128 a0005c0007t0001g0179 |
2 | HG02056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.215-1647T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585612 | |||||||
| chr11:585612 | T | TTGAGGTA others(16): Show |
1 | a0019c0028t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.215-1625_215-1624i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585612 | ||||||
| chr11:585635 | T | A | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-1624T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585635 | |||||||
| chr11:585635 | T | TTGAGGTA others(890): Show |
1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.215-1612_215-1611i others(899): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585635 | ||||||
| chr11:585640 | G | A | 34 | a0001c0001t0001g0072 a0001c0001t0001g0256 a0001c0027t0001g0253 others(31): Show |
37 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.215-1619G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585640 | |||||||
| chr11:585658 | T | A | 120 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0102 others(117): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.215-1601T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585658 | |||||||
| chr11:585658 | T | TTGAGGTA others(16): Show |
1 | a0001c0001t0001g0201 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4892): Show |
1 | a0001c0023t0001g0230 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4901): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4593): Show |
1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4602): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4593): Show |
1 | a0001c0001t0001g0235 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4602): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4708): Show |
1 | a0001c0001t0001g0163 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4731): Show |
1 | a0001c0001t0001g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(6272): Show |
1 | a0001c0001t0001g0264 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6281): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(6295): Show |
1 | a0001c0001t0001g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6304): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0236 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0061 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4731): Show |
1 | a0001c0001t0001g0115 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4731): Show |
1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(3880): Show |
1 | a0001c0001t0001g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(3889): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0239 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0154 |
2 | HG00558.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0142 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0075 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0200 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4823): Show |
1 | a0015c0036t0001g0111 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(6111): Show |
1 | a0001c0033t0010g0106 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6120): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0062 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4662): Show |
1 | a0001c0001t0001g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4671): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(5904): Show |
1 | a0001c0001t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(5913): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4640): Show |
1 | a0001c0001t0001g0148 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4649): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(3167): Show |
1 | a0001c0014t0001g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(3176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(3167): Show |
3 | a0001c0014t0001g0261 a0001c0014t0001g0262 a0001c0031t0001g0260 |
3 | HG01943.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(3176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4685): Show |
1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4708): Show |
1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4593): Show |
1 | a0001c0001t0001g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4602): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0078 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0001g0164 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4869): Show |
1 | a0001c0001t0001g0065 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4878): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4685): Show |
2 | a0001c0001t0001g0063 a0001c0001t0001g0077 |
2 | HG00438.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4547): Show |
1 | a0001c0001t0001g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4556): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(6180): Show |
1 | a0001c0001t0001g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6189): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4547): Show |
1 | a0001c0001t0001g0108 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4556): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
4 | NA18948.hp2 NA18963.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0008 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4778): Show |
1 | a0001c0001t0001g0240 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4787): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0001g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4984): Show |
1 | a0001c0001t0001g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4993): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4961): Show |
1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4970): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4179): Show |
1 | a0001c0001t0001g0204 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4188): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0118 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4662): Show |
1 | a0011c0017t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4671): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4294): Show |
1 | a0001c0001t0001g0101 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4303): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4685): Show |
1 | a0011c0017t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(2960): Show |
1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(2969): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4756): Show |
1 | a0021c0035t0001g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4765): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0020c0032t0001g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4708): Show |
1 | a0001c0034t0001g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4777): Show |
2 | a0005c0007t0001g0251 a0005c0007t0001g0252 |
2 | HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4317): Show |
1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4326): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(2638): Show |
1 | a0001c0001t0001g0007 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(2647): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4685): Show |
1 | a0001c0001t0001g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4800): Show |
1 | a0001c0001t0001g0211 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4809): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(5007): Show |
1 | a0001c0001t0001g0160 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(5016): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4823): Show |
1 | a0001c0001t0001g0120 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4685): Show |
1 | a0001c0001t0001g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4777): Show |
1 | a0005c0007t0001g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(5053): Show |
1 | a0001c0001t0001g0238 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(5062): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4202): Show |
1 | a0018c0037t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4211): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4708): Show |
1 | a0005c0007t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0005c0007t0001g0128 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4754): Show |
1 | a0019c0028t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(3305): Show |
1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(3314): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0150 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(890): Show |
1 | a0002c0002t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(899): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(844): Show |
2 | a0001c0001t0001g0089 a0002c0002t0001g0134 |
2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(913): Show |
1 | a0002c0002t0001g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(922): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(821): Show |
1 | a0003c0004t0003g0189 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(913): Show |
5 | a0001c0009t0002g0095 a0001c0009t0002g0132 a0001c0009t0002g0182 others(2): Show |
6 | HG02451.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(922): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(936): Show |
1 | a0008c0013t0002g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(945): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(798): Show |
1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(798): Show |
2 | a0003c0004t0003g0221 a0003c0004t0003g0268 |
2 | HG01346.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(844): Show |
1 | a0002c0002t0001g0220 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(867): Show |
1 | a0002c0002t0001g0219 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(876): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(959): Show |
1 | a0002c0002t0001g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(968): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(936): Show |
3 | a0001c0001t0001g0092 a0002c0002t0001g0137 a0002c0002t0001g0187 |
3 | HG02723.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(945): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(913): Show |
2 | a0001c0001t0001g0131 a0001c0009t0007g0098 |
2 | HG01074.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(922): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(890): Show |
4 | a0002c0002t0001g0123 a0002c0002t0001g0169 a0002c0002t0001g0171 others(1): Show |
4 | HG00597.hp1 HG00609.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(899): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(867): Show |
5 | a0002c0002t0001g0002 a0002c0002t0001g0071 a0002c0002t0001g0170 others(2): Show |
7 | HG01167.hp1 HG01169.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(876): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(844): Show |
2 | a0002c0002t0001g0214 a0002c0002t0001g0217 |
2 | HG00280.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(821): Show |
3 | a0002c0002t0001g0060 a0002c0002t0001g0193 a0002c0002t0001g0257 |
3 | HG02080.hp2 HG03831.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(821): Show |
1 | a0001c0009t0002g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(729): Show |
1 | a0002c0002t0001g0173 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(844): Show |
4 | a0002c0011t0001g0059 a0002c0011t0001g0066 a0002c0011t0001g0166 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(5030): Show |
1 | a0001c0001t0001g0244 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.215-1585_215-1584i others(5039): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(4938): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0269 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.215-1585_215-1584i others(4947): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585658 | T | TTGAGGTA others(798): Show |
1 | a0002c0002t0001g0245 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.215-1585_215-1584i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | ||||||
| chr11:585680 | C | CT | 9 | a0001c0001t0001g0231 a0001c0001t0001g0237 a0001c0001t0001g0263 others(6): Show |
9 | HG00099.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-1561dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(1): Show |
6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1568_215-1561d others(10): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(3): Show |
6 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(3): Show |
7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1570_215-1561d others(12): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(4): Show |
2 | a0001c0006t0002g0017 a0003c0004t0003g0176 |
2 | HG01192.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.215-1571_215-1561d others(13): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(5): Show |
11 | a0001c0003t0002g0024 a0001c0003t0002g0029 a0001c0003t0002g0056 others(8): Show |
11 | HG00140.hp1 HG01257.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-1572_215-1561d others(14): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(6): Show |
23 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0028 others(20): Show |
24 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.215-1573_215-1561d others(15): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(7): Show |
10 | a0001c0003t0002g0021 a0001c0003t0002g0040 a0001c0003t0002g0049 others(7): Show |
10 | HG01074.hp2 HG01346.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-1574_215-1561d others(16): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(8): Show |
2 | a0001c0003t0002g0018 a0001c0003t0008g0051 |
2 | NA18967.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.215-1575_215-1561d others(17): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | C | CTTTTTTT others(9): Show |
1 | a0001c0003t0002g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.215-1576_215-1561d others(18): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585680 | CT | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0161 a0001c0001t0001g0197 others(4): Show |
7 | HG01943.hp1 HG03710.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1561delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | ||||||
| chr11:585744 | G | C | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-1515G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585744 | |||||||
| chr11:585824 | G | A | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1435G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585824 | |||||||
| chr11:585857 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1402T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585857 | |||||||
| chr11:586050 | G | A | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.215-1209G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586050 | |||||||
| chr11:586129 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1130A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586129 | |||||||
| chr11:586185 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.215-1074G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586185 | |||||||
| chr11:586334 | A | T | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-925A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586334 | |||||||
| chr11:586417 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-842C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586417 | |||||||
| chr11:586564 | A | G | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.215-695A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586564 | |||||||
| chr11:586635 | G | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-624G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586635 | |||||||
| chr11:586661 | C | CT | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-597dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 586661 | ||||||
| chr11:586696 | A | G | 51 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.215-563A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586696 | |||||||
| chr11:586698 | C | G | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.215-561C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586698 | |||||||
| chr11:586833 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.215-426T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586833 | |||||||
| chr11:587014 | C | T | 37 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0078 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.215-245C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 587014 | |||||||
| chr11:587238 | G | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-21G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 587238 | |||||||
| chr11:587528 | C | T | 1 | a0021c0035t0001g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.420+64C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587528 | |||||||
| chr11:587655 | CAT | C | 3 | a0001c0001t0001g0089 a0002c0002t0001g0133 a0002c0002t0001g0134 |
3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.420+192_420+193del others(2): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587655 | |||||||
| chr11:587700 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+236T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587700 | |||||||
| chr11:587885 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.420+421A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587885 | |||||||
| chr11:588067 | G | A | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.420+603G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588067 | |||||||
| chr11:588192 | CCTGTT | C | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.420+734_420+738del others(5): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 588192 | ||||||
| chr11:588289 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+825T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588289 | |||||||
| chr11:588292 | C | T | 1 | a0006c0010t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.420+828C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588292 | |||||||
| chr11:588306 | C | T | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.420+842C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588306 | |||||||
| chr11:588377 | C | CT | 12 | a0002c0002t0001g0002 a0002c0002t0001g0067 a0002c0002t0001g0123 others(9): Show |
14 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+924dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 588377 | ||||||
| chr11:588489 | C | G | 2 | a0003c0004t0003g0221 a0003c0004t0003g0268 |
2 | HG01346.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.420+1025C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588489 | |||||||
| chr11:588504 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+1040C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588504 | |||||||
| chr11:588505 | G | A | 1 | a0002c0002t0001g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.420+1041G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588505 | |||||||
| chr11:588617 | G | A | 1 | a0022c0026t0001g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.420+1153G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588617 | |||||||
| chr11:588654 | C | T | 117 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.420+1190C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588654 | |||||||
| chr11:588659 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0142 others(3): Show |
6 | HG00741.hp1 HG01099.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+1195G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588659 | |||||||
| chr11:589029 | G | C | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.420+1565G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589029 | |||||||
| chr11:589072 | G | A | 1 | a0002c0002t0001g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.420+1608G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589072 | |||||||
| chr11:589076 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+1612C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589076 | |||||||
| chr11:589113 | C | T | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.420+1649C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589113 | |||||||
| chr11:589162 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+1698G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589162 | |||||||
| chr11:589246 | G | A | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.420+1782G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589246 | |||||||
| chr11:589392 | T | G | 2 | a0001c0003t0002g0015 a0001c0003t0002g0046 |
2 | HG01192.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.420+1928T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589392 | |||||||
| chr11:589538 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.421-1846G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589538 | |||||||
| chr11:589564 | T | C | 189 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(186): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.421-1820T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589564 | |||||||
| chr11:589570 | C | A | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.421-1814C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589570 | |||||||
| chr11:589579 | G | GGA | 181 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.421-1804_421-1803i others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589579 | ||||||
| chr11:589581 | G | A | 181 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.421-1803G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589581 | |||||||
| chr11:589589 | C | T | 10 | a0001c0001t0001g0072 a0003c0008t0004g0081 a0003c0008t0004g0082 others(7): Show |
10 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-1795C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589589 | |||||||
| chr11:589595 | T | A | 12 | a0001c0001t0001g0072 a0001c0009t0002g0182 a0002c0002t0001g0087 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1789T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589595 | |||||||
| chr11:589597 | G | A | 13 | a0001c0001t0001g0072 a0001c0009t0002g0182 a0002c0002t0001g0087 others(10): Show |
13 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1787G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589597 | |||||||
| chr11:589619 | T | C | 1 | a0001c0006t0002g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.421-1765T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589619 | |||||||
| chr11:589639 | C | T | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1745C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589639 | |||||||
| chr11:589641 | G | C | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1743G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589641 | |||||||
| chr11:589643 | C | T | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1741C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589643 | |||||||
| chr11:589647 | G | T | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1737G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589647 | |||||||
| chr11:589659 | G | A | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1725G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589659 | |||||||
| chr11:589661 | C | T | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1723C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589661 | |||||||
| chr11:589662 | T | C | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1722T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589662 | |||||||
| chr11:589673 | G | A | 13 | a0001c0006t0002g0009 a0001c0006t0002g0010 a0003c0004t0003g0189 others(10): Show |
13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1711G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589673 | |||||||
| chr11:589747 | A | G | 1 | a0004c0005t0002g0035 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.421-1637A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589747 | |||||||
| chr11:589748 | G | T | 9 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-1636G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589748 | |||||||
| chr11:589752 | C | T | 9 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-1632C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589752 | |||||||
| chr11:589792 | G | A | 8 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1592G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589792 | |||||||
| chr11:589794 | T | A | 8 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1590T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589794 | |||||||
| chr11:589804 | C | T | 8 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1580C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589804 | |||||||
| chr11:589810 | C | T | 8 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1574C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589810 | |||||||
| chr11:589811 | A | AGAGCGTG others(126): Show |
1 | a0001c0009t0002g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.421-1566_421-1565i others(135): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589811 | ||||||
| chr11:589811 | A | G | 11 | a0001c0003t0002g0016 a0003c0004t0003g0176 a0003c0008t0004g0081 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-1573A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589811 | |||||||
| chr11:589816 | G | A | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1568G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589816 | |||||||
| chr11:589819 | C | T | 52 | a0001c0001t0001g0201 a0001c0003t0002g0015 a0001c0003t0002g0018 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.421-1565C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589819 | |||||||
| chr11:589820 | G | C | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1564G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589820 | |||||||
| chr11:589821 | G | A | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1563G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589821 | |||||||
| chr11:589831 | TGAGA | T | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1547_421-1544d others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589831 | ||||||
| chr11:589838 | G | A | 2 | a0001c0001t0001g0209 a0001c0003t0002g0016 |
2 | HG01069.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.421-1546G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589838 | |||||||
| chr11:589839 | A | AGTCTGCA others(81): Show |
4 | a0001c0014t0001g0261 a0001c0014t0001g0262 a0001c0031t0001g0260 others(1): Show |
4 | HG01943.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-1503_421-1416d others(90): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589839 | ||||||
| chr11:589839 | A | AGTCTGCA others(167): Show |
2 | a0001c0009t0002g0132 a0002c0011t0001g0066 |
2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.421-1539_421-1366d others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589839 | ||||||
| chr11:589839 | A | T | 2 | a0001c0001t0001g0209 a0001c0003t0002g0016 |
2 | HG01069.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.421-1545A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589839 | |||||||
| chr11:589849 | C | T | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1535C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589849 | |||||||
| chr11:589855 | C | CAGAGCGT others(167): Show |
1 | a0001c0001t0001g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.421-1529_421-1528i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589855 | |||||||
| chr11:589855 | C | CGGAGCGT others(167): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0264 |
2 | HG01167.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.421-1481_421-1480i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589855 | ||||||
| chr11:589855 | C | CGGAGCGT others(167): Show |
93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.421-1366_421-1365i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589855 | ||||||
| chr11:589855 | C | CGGAGCGT others(166): Show |
1 | a0001c0001t0001g0120 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.421-1459_421-1458i others(175): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589855 | ||||||
| chr11:589855 | C | T | 3 | a0001c0001t0001g0209 a0001c0003t0002g0016 a0003c0020t0006g0248 |
3 | HG01069.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-1529C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589855 | |||||||
| chr11:589865 | G | A | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1519G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589865 | |||||||
| chr11:589869 | C | T | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1515C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589869 | |||||||
| chr11:589876 | T | TGA | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1505_421-1504d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589876 | ||||||
| chr11:589881 | A | G | 12 | a0001c0003t0002g0016 a0003c0008t0004g0081 a0003c0008t0004g0082 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1503A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589881 | |||||||
| chr11:589881 | ATGTCTGC others(38): Show |
A | 1 | a0003c0004t0003g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.421-1486_421-1442d others(47): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589881 | ||||||
| chr11:589882 | T | A | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1502T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589882 | |||||||
| chr11:589898 | T | C | 2 | a0001c0003t0002g0016 a0003c0020t0006g0248 |
2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-1486T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589898 | |||||||
| chr11:589898 | T | TGGAGCGT others(210): Show |
1 | a0010c0019t0001g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.421-1366_421-1365i others(219): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589898 | ||||||
| chr11:589907 | C | T | 12 | a0001c0006t0002g0017 a0003c0008t0004g0081 a0003c0008t0004g0082 others(9): Show |
12 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1477C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589907 | |||||||
| chr11:589908 | A | G | 14 | a0001c0003t0002g0016 a0001c0006t0002g0017 a0003c0008t0004g0081 others(11): Show |
14 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-1476A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589908 | |||||||
| chr11:589912 | T | C | 14 | a0001c0003t0002g0016 a0001c0006t0002g0017 a0003c0008t0004g0081 others(11): Show |
14 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-1472T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589912 | |||||||
| chr11:589923 | AGG | A | 12 | a0001c0006t0002g0017 a0003c0008t0004g0081 a0003c0008t0004g0082 others(9): Show |
12 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1459_421-1458d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589923 | ||||||
| chr11:589925 | G | A | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1459G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589925 | |||||||
| chr11:589926 | G | A | 12 | a0001c0006t0002g0017 a0003c0008t0004g0081 a0003c0008t0004g0082 others(9): Show |
12 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1458G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589926 | |||||||
| chr11:589927 | T | A | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1457T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589927 | |||||||
| chr11:589943 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1441C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589943 | |||||||
| chr11:589952 | C | T | 2 | a0001c0003t0002g0016 a0003c0020t0006g0248 |
2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-1432C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589952 | |||||||
| chr11:589953 | G | A | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1431G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589953 | |||||||
| chr11:589957 | C | T | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1427C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589957 | |||||||
| chr11:589968 | A | AATGTCTG others(40): Show |
1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1416_421-1415i others(49): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589968 | |||||||
| chr11:589968 | A | AGGGT | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1415_421-1414i others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589968 | ||||||
| chr11:589968 | A | T | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1416A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589968 | |||||||
| chr11:589984 | C | T | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1400C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589984 | |||||||
| chr11:589993 | T | C | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1391T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589993 | |||||||
| chr11:590012 | G | A | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1372G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590012 | |||||||
| chr11:590012 | GTGTCTGT others(36): Show |
G | 4 | a0003c0004t0003g0176 a0007c0012t0003g0068 a0007c0012t0003g0083 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-1365_421-1323d others(45): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590012 | ||||||
| chr11:590019 | T | C | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.421-1365T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590019 | |||||||
| chr11:590029 | T | C | 1 | a0001c0003t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1355T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590029 | |||||||
| chr11:590029 | T | TGGAGCGT others(36): Show |
37 | a0001c0003t0002g0015 a0001c0003t0002g0018 a0001c0003t0002g0021 others(34): Show |
38 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.421-1313_421-1312i others(45): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590029 | ||||||
| chr11:590029 | T | TGGAGCGT others(298): Show |
1 | a0001c0003t0002g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.421-1313_421-1312i others(307): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590029 | ||||||
| chr11:590072 | T | C | 86 | a0001c0001t0001g0089 a0001c0003t0002g0015 a0001c0003t0002g0016 others(83): Show |
89 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.421-1312T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590072 | |||||||
| chr11:590072 | T | TGGAGCGT others(167): Show |
9 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0142 others(6): Show |
10 | HG00741.hp1 HG01099.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-1303_421-1302i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590072 | ||||||
| chr11:590102 | G | C | 37 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0078 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.421-1282G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590102 | |||||||
| chr11:590107 | A | C | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.421-1277A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590107 | |||||||
| chr11:590116 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421-1268G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590116 | |||||||
| chr11:590201 | C | T | 36 | a0001c0001t0001g0201 a0001c0001t0001g0256 a0001c0027t0001g0253 others(33): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.421-1183C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590201 | |||||||
| chr11:590425 | C | T | 2 | a0002c0002t0001g0224 a0002c0002t0001g0225 |
2 | NA18941.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.421-959C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590425 | |||||||
| chr11:590517 | A | T | 1 | a0001c0014t0001g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421-867A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590517 | |||||||
| chr11:590534 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-850A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590534 | |||||||
| chr11:590605 | C | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(30): Show |
33 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.421-779C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590605 | |||||||
| chr11:590648 | A | G | 71 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(68): Show |
74 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.421-736A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590648 | |||||||
| chr11:590660 | A | C | 1 | a0002c0002t0001g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.421-724A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590660 | |||||||
| chr11:590665 | T | A | 1 | a0002c0002t0001g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.421-719T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590665 | |||||||
| chr11:590666 | A | T | 1 | a0002c0002t0001g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.421-718A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590666 | |||||||
| chr11:590728 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-656A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590728 | |||||||
| chr11:590775 | C | G | 5 | a0001c0006t0002g0020 a0001c0006t0002g0022 a0001c0006t0002g0038 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-609C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590775 | |||||||
| chr11:590945 | T | G | 3 | a0001c0001t0001g0089 a0002c0002t0001g0133 a0002c0002t0001g0134 |
3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.421-439T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590945 | |||||||
| chr11:590999 | G | A | 60 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(57): Show |
62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.421-385G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590999 | |||||||
| chr11:591083 | G | A | 208 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(205): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.421-301G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 591083 | |||||||
| chr11:591180 | G | T | 3 | a0003c0004t0003g0189 a0003c0004t0003g0221 a0003c0004t0003g0268 |
3 | HG01346.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.421-204G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 591180 | |||||||
| chr11:591480 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.504+13G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591480 | |||||||
| chr11:591601 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.504+134G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591601 | |||||||
| chr11:591907 | C | G | 1 | a0002c0002t0001g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.504+440C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591907 | |||||||
| chr11:591908 | G | C | 1 | a0002c0002t0001g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.504+441G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591908 | |||||||
| chr11:591912 | G | GT | 39 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(36): Show |
39 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+462dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 591912 | ||||||
| chr11:591912 | GT | G | 17 | a0001c0001t0001g0202 a0001c0009t0002g0132 a0001c0009t0002g0182 others(14): Show |
18 | HG00280.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.504+462delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 591912 | ||||||
| chr11:591932 | C | T | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.504+465C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591932 | |||||||
| chr11:591980 | A | G | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.504+513A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591980 | |||||||
| chr11:592023 | G | C | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.505-536G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592023 | |||||||
| chr11:592080 | T | A | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.505-479T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592080 | |||||||
| chr11:592106 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0200 |
2 | HG00597.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.505-453G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592106 | |||||||
| chr11:592136 | C | T | 3 | a0001c0006t0002g0020 a0001c0006t0002g0022 a0001c0006t0002g0038 |
3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.505-423C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592136 | |||||||
| chr11:592140 | C | T | 1 | a0018c0037t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.505-419C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592140 | |||||||
| chr11:592214 | C | CT | 14 | a0001c0001t0001g0101 a0001c0003t0002g0046 a0003c0004t0003g0006 others(11): Show |
15 | HG00639.hp2 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.505-327dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 592214 | ||||||
| chr11:592222 | T | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-337T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592222 | |||||||
| chr11:592250 | C | T | 1 | a0003c0004t0003g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.505-309C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592250 | |||||||
| chr11:592254 | C | T | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.505-305C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592254 | |||||||
| chr11:592306 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.505-253G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592306 | |||||||
| chr11:592329 | G | A | 1 | a0002c0011t0001g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.505-230G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592329 | |||||||
| chr11:592377 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-182C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592377 | |||||||
| chr11:592388 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.505-171T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592388 | |||||||
| chr11:592406 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-153C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592406 | |||||||
| chr11:592415 | C | T | 1 | a0001c0009t0002g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.505-144C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592415 | |||||||
| chr11:592510 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-49T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592510 | |||||||
| chr11:592700 | C | T | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620+26C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592700 | |||||||
| chr11:592825 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.620+151G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592825 | |||||||
| chr11:592873 | A | G | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.620+199A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592873 | |||||||
| chr11:592902 | A | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | NA18943.hp2 NA19002.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.620+228A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592902 | |||||||
| chr11:593008 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+334A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593008 | |||||||
| chr11:593042 | C | G | 4 | a0006c0010t0002g0011 a0006c0010t0002g0012 a0006c0010t0002g0013 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+368C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593042 | |||||||
| chr11:593098 | C | T | 11 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(8): Show |
12 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+424C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593098 | |||||||
| chr11:593219 | G | A | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.620+545G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593219 | |||||||
| chr11:593453 | T | C | 124 | a0001c0001t0001g0201 a0001c0001t0001g0256 a0001c0003t0002g0015 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.620+779T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593453 | |||||||
| chr11:593572 | C | G | 1 | a0002c0002t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.620+898C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593572 | |||||||
| chr11:593827 | A | G | 1 | a0002c0002t0001g0254 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.620+1153A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593827 | |||||||
| chr11:593962 | C | T | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+1288C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593962 | |||||||
| chr11:594005 | T | C | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620+1331T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594005 | |||||||
| chr11:594069 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.620+1395G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594069 | |||||||
| chr11:594072 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.620+1398T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594072 | |||||||
| chr11:594196 | G | A | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.620+1522G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594196 | |||||||
| chr11:594264 | A | G | 4 | a0002c0011t0001g0059 a0002c0011t0001g0066 a0002c0011t0001g0166 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+1590A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594264 | |||||||
| chr11:594273 | T | TAGAG | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1602_620+1603i others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 594273 | ||||||
| chr11:594329 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1655C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594329 | |||||||
| chr11:594414 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.620+1740T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594414 | |||||||
| chr11:594422 | T | A | 1 | a0001c0003t0008g0051 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.620+1748T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594422 | |||||||
| chr11:594481 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1807G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594481 | |||||||
| chr11:594535 | G | A | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+1861G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594535 | |||||||
| chr11:594609 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1935A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594609 | |||||||
| chr11:594650 | C | T | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.620+1976C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594650 | |||||||
| chr11:594698 | T | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+2024T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594698 | |||||||
| chr11:594894 | TAAAAC | T | 104 | a0001c0001t0001g0201 a0001c0001t0001g0256 a0001c0003t0002g0015 others(101): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.621-2026_621-2022d others(7): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 594894 | ||||||
| chr11:594909 | A | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0237 |
2 | NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.621-2014A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594909 | |||||||
| chr11:595093 | C | T | 1 | a0007c0012t0003g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.621-1830C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595093 | |||||||
| chr11:595168 | A | T | 250 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.621-1755A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595168 | |||||||
| chr11:595184 | G | C | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.621-1739G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595184 | |||||||
| chr11:595209 | G | A | 14 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(11): Show |
14 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.621-1714G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595209 | |||||||
| chr11:595305 | A | G | 10 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(7): Show |
10 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.621-1618A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595305 | |||||||
| chr11:595314 | CA | C | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.621-1602delA | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 595314 | ||||||
| chr11:595362 | CA | C | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-1560delA | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595362 | |||||||
| chr11:595683 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.621-1240C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595683 | |||||||
| chr11:595810 | A | G | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.621-1113A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595810 | |||||||
| chr11:595890 | G | A | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.621-1033G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595890 | |||||||
| chr11:595894 | C | T | 1 | a0010c0019t0001g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.621-1029C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595894 | |||||||
| chr11:595940 | C | T | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.621-983C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595940 | |||||||
| chr11:595992 | A | G | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.621-931A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595992 | |||||||
| chr11:596002 | A | G | 1 | a0002c0011t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.621-921A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596002 | |||||||
| chr11:596005 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-918A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596005 | |||||||
| chr11:596035 | G | A | 7 | a0005c0007t0001g0128 a0005c0007t0001g0251 a0005c0007t0001g0252 others(4): Show |
7 | HG02004.hp2 HG02040.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.621-888G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596035 | |||||||
| chr11:596091 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.621-832C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596091 | |||||||
| chr11:596102 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.621-821G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596102 | |||||||
| chr11:596118 | G | T | 1 | a0022c0026t0001g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.621-805G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596118 | |||||||
| chr11:596248 | G | A | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.621-675G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596248 | |||||||
| chr11:596299 | C | G | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-624C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596299 | |||||||
| chr11:596303 | C | T | 1 | a0020c0032t0001g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.621-620C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596303 | |||||||
| chr11:596309 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-614A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596309 | |||||||
| chr11:596480 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-443T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596480 | |||||||
| chr11:596499 | G | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-424G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596499 | |||||||
| chr11:596518 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.621-405C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596518 | |||||||
| chr11:596672 | G | T | 37 | a0001c0001t0001g0201 a0001c0001t0001g0256 a0001c0027t0001g0253 others(34): Show |
39 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.621-251G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596672 | |||||||
| chr11:596842 | G | A | 10 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(7): Show |
10 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.621-81G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596842 | |||||||
| chr11:596866 | A | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-57A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596866 | |||||||
| chr11:597064 | A | G | 1 | a0015c0036t0001g0111 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.718+44A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597064 | |||||||
| chr11:597074 | C | T | 5 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0012c0016t0001g0070 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+54C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597074 | |||||||
| chr11:597153 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.718+133G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597153 | |||||||
| chr11:597318 | G | A | 2 | a0001c0001t0001g0008 a0001c0033t0010g0106 |
2 | NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.719-77G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597318 | |||||||
| chr11:597348 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.719-47C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597348 | |||||||
| chr11:597349 | G | A | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.719-46G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597349 | |||||||
| chr11:597597 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.894+27C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 597597 | |||||||
| chr11:597815 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.894+245C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 597815 | |||||||
| chr11:597868 | C | T | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.894+298C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 597868 | |||||||
| chr11:598033 | C | T | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.895-340C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598033 | |||||||
| chr11:598148 | C | T | 3 | a0003c0004t0003g0027 a0003c0004t0003g0215 a0003c0004t0003g0249 |
3 | HG01884.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.895-225C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598148 | |||||||
| chr11:598205 | C | G | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.895-168C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598205 | |||||||
| chr11:598288 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.895-85G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598288 | |||||||
| chr11:598288 | G | C | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.895-85G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598288 | |||||||
| chr11:598595 | C | G | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1024+93C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598595 | |||||||
| chr11:598723 | A | C | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1024+221A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598723 | |||||||
| chr11:598793 | C | T | 3 | a0007c0012t0003g0068 a0007c0012t0003g0083 a0007c0012t0003g0175 |
3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1024+291C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598793 | |||||||
| chr11:598852 | C | G | 1 | a0002c0002t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1024+350C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598852 | |||||||
| chr11:598874 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1024+372A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598874 | |||||||
| chr11:598879 | A | G | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1024+377A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598879 | |||||||
| chr11:599132 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1024+630G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599132 | |||||||
| chr11:599253 | C | CT | 28 | a0001c0001t0001g0102 a0001c0001t0001g0143 a0001c0001t0001g0150 others(25): Show |
29 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024+770dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 599253 | ||||||
| chr11:599253 | CT | C | 71 | a0001c0001t0001g0089 a0001c0001t0001g0154 a0001c0001t0001g0213 others(68): Show |
73 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1024+770delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 599253 | ||||||
| chr11:599280 | A | T | 1 | a0005c0007t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1024+778A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599280 | |||||||
| chr11:599287 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+785C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599287 | |||||||
| chr11:599313 | T | C | 82 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(79): Show |
85 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1024+811T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599313 | |||||||
| chr11:599471 | G | A | 11 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(8): Show |
12 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+969G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599471 | |||||||
| chr11:599481 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1024+979C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599481 | |||||||
| chr11:599542 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+1040T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599542 | |||||||
| chr11:599588 | C | T | 4 | a0005c0007t0001g0090 a0005c0007t0001g0129 a0005c0007t0001g0178 others(1): Show |
4 | HG01168.hp2 HG02056.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1086C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599588 | |||||||
| chr11:599654 | T | C | 4 | a0003c0020t0006g0248 a0007c0012t0003g0068 a0007c0012t0003g0083 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1152T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599654 | |||||||
| chr11:599668 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+1166A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599668 | |||||||
| chr11:599700 | C | T | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1024+1198C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599700 | |||||||
| chr11:599711 | G | A | 1 | a0001c0023t0001g0230 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1024+1209G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599711 | |||||||
| chr11:599779 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+1277A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599779 | |||||||
| chr11:600097 | T | C | 1 | a0002c0002t0001g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1025-1477T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600097 | |||||||
| chr11:600098 | C | T | 1 | a0002c0002t0001g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1025-1476C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600098 | |||||||
| chr11:600222 | C | G | 11 | a0005c0007t0001g0090 a0005c0007t0001g0128 a0005c0007t0001g0129 others(8): Show |
11 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025-1352C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600222 | |||||||
| chr11:600254 | C | CT | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-1306dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600254 | ||||||
| chr11:600379 | C | T | 1 | a0002c0002t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1025-1195C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600379 | |||||||
| chr11:600474 | G | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0067 a0002c0002t0001g0123 others(8): Show |
13 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1025-1100G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600474 | |||||||
| chr11:600493 | A | AAT | 48 | a0001c0001t0001g0201 a0001c0001t0001g0256 a0001c0003t0002g0018 others(45): Show |
53 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1025-1056_1025-105 others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATAAATA others(27): Show |
4 | a0003c0020t0006g0248 a0007c0012t0003g0068 a0007c0012t0003g0083 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025-1078_1025-107 others(38): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATAAATA others(31): Show |
1 | a0003c0008t0004g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025-1078_1025-107 others(42): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATAAATA others(35): Show |
5 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025-1078_1025-107 others(46): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATAAATA others(9): Show |
1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1025-1078_1025-107 others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATAAATA others(15): Show |
1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1025-1078_1025-107 others(26): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATAT | 13 | a0002c0002t0001g0060 a0002c0002t0001g0067 a0002c0002t0001g0123 others(10): Show |
13 | HG00597.hp1 HG00609.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1025-1058_1025-105 others(8): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATATATA others(1): Show |
5 | a0001c0009t0002g0132 a0003c0004t0003g0189 a0003c0004t0003g0221 others(2): Show |
5 | HG01346.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-1062_1025-105 others(12): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | A | AATATATA others(3): Show |
1 | a0001c0009t0002g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1025-1064_1025-105 others(14): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | AAT | A | 102 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(99): Show |
102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1025-1056_1025-105 others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600493 | AATAT | A | 7 | a0001c0001t0001g0235 a0001c0001t0001g0270 a0002c0002t0001g0086 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025-1058_1025-105 others(8): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | ||||||
| chr11:600512 | A | G | 11 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025-1062A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600512 | |||||||
| chr11:600647 | T | C | 1 | a0001c0006t0002g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1025-927T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600647 | |||||||
| chr11:600693 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-881A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600693 | |||||||
| chr11:600790 | C | G | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1025-784C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600790 | |||||||
| chr11:600846 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-728G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600846 | |||||||
| chr11:600906 | C | T | 1 | a0013c0021t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1025-668C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600906 | |||||||
| chr11:601145 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1025-429C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 601145 | |||||||
| chr11:601428 | C | CA | 31 | a0001c0001t0001g0064 a0001c0001t0001g0108 a0001c0001t0001g0143 others(28): Show |
32 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1025-128dupA | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 601428 | ||||||
| chr11:601470 | C | T | 3 | a0001c0001t0001g0089 a0002c0002t0001g0133 a0002c0002t0001g0134 |
3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1025-104C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 601470 | |||||||
| chr11:601479 | G | A | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1025-95G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 601479 | |||||||
| chr11:601785 | T | C | 71 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(68): Show |
73 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1152+84T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601785 | |||||||
| chr11:601803 | G | A | 3 | a0001c0006t0002g0020 a0001c0006t0002g0022 a0001c0006t0002g0038 |
3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1152+102G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601803 | |||||||
| chr11:601804 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1152+103C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601804 | |||||||
| chr11:601953 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+252A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601953 | |||||||
| chr11:601985 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+284A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601985 | |||||||
| chr11:601986 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+285G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601986 | |||||||
| chr11:601987 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+286C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601987 | |||||||
| chr11:601988 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+287T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601988 | |||||||
| chr11:601990 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+289G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601990 | |||||||
| chr11:601997 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+296A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601997 | |||||||
| chr11:601998 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+297G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601998 | |||||||
| chr11:602006 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+305T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602006 | |||||||
| chr11:602007 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+306G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602007 | |||||||
| chr11:602009 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+308G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602009 | |||||||
| chr11:602013 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+312G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602013 | |||||||
| chr11:602014 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+313G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602014 | |||||||
| chr11:602030 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+329T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602030 | |||||||
| chr11:602036 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+335A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602036 | |||||||
| chr11:602045 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+344G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602045 | |||||||
| chr11:602046 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+345G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602046 | |||||||
| chr11:602048 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+347G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602048 | |||||||
| chr11:602054 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+353G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602054 | |||||||
| chr11:602057 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+356G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602057 | |||||||
| chr11:602059 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+358T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602059 | |||||||
| chr11:602061 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+360T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602061 | |||||||
| chr11:602065 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+364G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602065 | |||||||
| chr11:602066 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+365C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602066 | |||||||
| chr11:602068 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+367G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602068 | |||||||
| chr11:602071 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+370C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602071 | |||||||
| chr11:602073 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+372G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602073 | |||||||
| chr11:602074 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+373G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602074 | |||||||
| chr11:602080 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+379C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602080 | |||||||
| chr11:602081 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+380T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602081 | |||||||
| chr11:602082 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+381G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602082 | |||||||
| chr11:602083 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+382G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602083 | |||||||
| chr11:602085 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+384T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602085 | |||||||
| chr11:602091 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+390G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602091 | |||||||
| chr11:602093 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+392G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602093 | |||||||
| chr11:602094 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+393T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602094 | |||||||
| chr11:602095 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+394G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602095 | |||||||
| chr11:602099 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+398C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602099 | |||||||
| chr11:602102 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+401G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602102 | |||||||
| chr11:602103 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+402C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602103 | |||||||
| chr11:602105 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+404G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602105 | |||||||
| chr11:602106 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+405T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602106 | |||||||
| chr11:602108 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+407T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602108 | |||||||
| chr11:602114 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+413A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602114 | |||||||
| chr11:602116 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+415G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602116 | |||||||
| chr11:602130 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+429T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602130 | |||||||
| chr11:602131 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+430T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602131 | |||||||
| chr11:602134 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+433G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602134 | |||||||
| chr11:602136 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+435C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602136 | |||||||
| chr11:602150 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+449G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602150 | |||||||
| chr11:602151 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+450C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602151 | |||||||
| chr11:602154 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+453T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602154 | |||||||
| chr11:602166 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+465C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602166 | |||||||
| chr11:602238 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1152+537T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602238 | |||||||
| chr11:602300 | G | A | 1 | a0003c0004t0003g0006 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1152+599G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602300 | |||||||
| chr11:602321 | A | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+620A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602321 | |||||||
| chr11:602322 | A | G | 37 | a0001c0001t0001g0201 a0001c0001t0001g0256 a0001c0027t0001g0253 others(34): Show |
39 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1152+621A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602322 | |||||||
| chr11:602406 | C | T | 1 | a0001c0014t0001g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1152+705C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602406 | |||||||
| chr11:602594 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+893C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602594 | |||||||
| chr11:602749 | GGTTTTGT others(4): Show |
G | 4 | a0003c0020t0006g0248 a0007c0012t0003g0068 a0007c0012t0003g0083 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1054_1152+106 others(15): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 602749 | ||||||
| chr11:602749 | GGTTTTGT others(6): Show |
G | 2 | a0013c0021t0002g0250 a0013c0022t0002g0124 |
2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1152+1049_1152+106 others(17): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602749 | |||||||
| chr11:602751 | TTTTGTTT others(3): Show |
T | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152+1054_1152+106 others(14): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 602751 | ||||||
| chr11:602770 | G | GT | 12 | a0001c0001t0001g0064 a0001c0001t0001g0163 a0001c0001t0001g0232 others(9): Show |
12 | HG00735.hp1 HG01074.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+1080dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 602770 | ||||||
| chr11:602770 | G | T | 21 | a0001c0001t0001g0162 a0003c0008t0004g0081 a0003c0008t0004g0082 others(18): Show |
21 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.1152+1069G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602770 | |||||||
| chr11:602920 | G | A | 2 | a0002c0002t0001g0137 a0002c0002t0001g0187 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1152+1219G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602920 | |||||||
| chr11:602963 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1152+1262A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602963 | |||||||
| chr11:603119 | A | G | 3 | a0001c0001t0001g0089 a0002c0002t0001g0133 a0002c0002t0001g0134 |
3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1152+1418A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603119 | |||||||
| chr11:603167 | C | A | 1 | a0002c0002t0001g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1466C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603167 | |||||||
| chr11:603168 | A | C | 1 | a0002c0002t0001g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1467A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603168 | |||||||
| chr11:603339 | T | A | 1 | a0002c0002t0001g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1638T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603339 | |||||||
| chr11:603340 | A | G | 1 | a0002c0002t0001g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1639A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603340 | |||||||
| chr11:603369 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0079 |
2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1152+1668G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603369 | |||||||
| chr11:603413 | C | A | 269 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(266): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1153-1706C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603413 | |||||||
| chr11:603476 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1153-1643C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603476 | |||||||
| chr11:603724 | AGTTT | A | 7 | a0003c0008t0004g0082 a0003c0008t0004g0122 a0003c0008t0004g0177 others(4): Show |
7 | HG02145.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153-1390_1153-138 others(8): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603724 | ||||||
| chr11:603728 | TG | T | 8 | a0003c0004t0003g0006 a0003c0004t0003g0084 a0003c0004t0003g0085 others(5): Show |
8 | HG00639.hp2 HG01169.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1153-1390delG | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603728 | |||||||
| chr11:603729 | G | GT | 58 | a0001c0001t0001g0072 a0001c0001t0001g0163 a0001c0001t0001g0201 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1153-1368dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603729 | ||||||
| chr11:603729 | GT | G | 103 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(100): Show |
103 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1153-1368delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603729 | ||||||
| chr11:603729 | GTT | G | 6 | a0001c0001t0001g0157 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG01891.hp2 HG02083.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-1369_1153-136 others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603729 | ||||||
| chr11:603776 | T | C | 63 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(60): Show |
65 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1153-1343T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603776 | |||||||
| chr11:603819 | C | T | 1 | a0001c0003t0002g0031 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1153-1300C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603819 | |||||||
| chr11:603822 | C | T | 4 | a0001c0014t0001g0145 a0001c0014t0001g0261 a0001c0014t0001g0262 others(1): Show |
4 | HG01943.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1297C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603822 | |||||||
| chr11:604029 | T | G | 43 | a0001c0001t0001g0163 a0001c0001t0001g0201 a0001c0001t0001g0212 others(40): Show |
46 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1153-1090T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604029 | |||||||
| chr11:604040 | G | A | 13 | a0001c0001t0001g0229 a0002c0002t0001g0002 a0002c0002t0001g0067 others(10): Show |
15 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1153-1079G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604040 | |||||||
| chr11:604257 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1153-862G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604257 | |||||||
| chr11:604344 | A | G | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153-775A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604344 | |||||||
| chr11:604438 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1153-681G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604438 | |||||||
| chr11:604663 | C | T | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-456C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604663 | |||||||
| chr11:604900 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0131 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1153-219C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604900 | |||||||
| chr11:604941 | G | A | 11 | a0001c0003t0002g0018 a0001c0003t0002g0024 a0001c0003t0002g0029 others(8): Show |
11 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-178G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604941 | |||||||
| chr11:604978 | A | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153-141A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604978 | |||||||
| chr11:605108 | A | G | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1153-11A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 605108 | |||||||
| chr11:605393 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1334+93G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 11/17 | chr11 | 605393 | |||||||
| chr11:605767 | T | C | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454+43T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605767 | |||||||
| chr11:605856 | T | C | 206 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1454+132T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605856 | |||||||
| chr11:605857 | G | A | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454+133G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605857 | |||||||
| chr11:605915 | A | G | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1454+191A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605915 | |||||||
| chr11:605999 | C | T | 13 | a0005c0007t0001g0090 a0005c0007t0001g0128 a0005c0007t0001g0129 others(10): Show |
13 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454+275C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605999 | |||||||
| chr11:606089 | G | A | 1 | a0002c0002t0001g0219 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455-353G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606089 | |||||||
| chr11:606156 | C | T | 12 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1455-286C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606156 | |||||||
| chr11:606224 | G | C | 25 | a0001c0001t0001g0143 a0001c0001t0001g0228 a0003c0004t0003g0006 others(22): Show |
26 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1455-218G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606224 | |||||||
| chr11:606245 | GCTCC | G | 25 | a0001c0001t0001g0143 a0001c0001t0001g0228 a0003c0004t0003g0006 others(22): Show |
26 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1455-181_1455-178d others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr11 | 606245 | ||||||
| chr11:606294 | C | T | 19 | a0001c0001t0001g0143 a0001c0001t0001g0228 a0003c0004t0003g0006 others(16): Show |
20 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1455-148C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606294 | |||||||
| chr11:606359 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0144 |
2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1455-83C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606359 | |||||||
| chr11:606360 | G | A | 1 | a0003c0020t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1455-82G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606360 | |||||||
| chr11:606399 | C | T | 23 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(20): Show |
24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-43C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606399 | |||||||
| chr11:606607 | T | C | 23 | a0003c0004t0003g0006 a0003c0004t0003g0027 a0003c0004t0003g0084 others(20): Show |
24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1609+11T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606607 | |||||||
| chr11:606629 | T | A | 1 | a0002c0002t0001g0254 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1609+33T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606629 | |||||||
| chr11:606656 | G | C | 206 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1609+60G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606656 | |||||||
| chr11:606749 | G | A | 58 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(55): Show |
60 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1609+153G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606749 | |||||||
| chr11:606770 | C | T | 11 | a0001c0003t0002g0018 a0001c0003t0002g0024 a0001c0003t0002g0029 others(8): Show |
11 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1609+174C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606770 | |||||||
| chr11:606850 | C | T | 1 | a0001c0003t0002g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1610-216C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606850 | |||||||
| chr11:606974 | C | G | 3 | a0004c0005t0002g0033 a0004c0005t0002g0036 a0004c0005t0002g0043 |
3 | HG01346.hp2 HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1610-92C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606974 | |||||||
| chr11:607050 | C | A | 3 | a0004c0005t0002g0033 a0004c0005t0002g0036 a0004c0005t0002g0043 |
3 | HG01346.hp2 HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1610-16C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 607050 | |||||||
| chr11:609728 | G | C | 3 | a0001c0006t0002g0020 a0001c0006t0002g0022 a0001c0006t0002g0038 |
3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.4264+8G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609728 | |||||||
| chr11:609729 | T | TGCCCCGG others(73): Show |
1 | a0001c0001t0001g0209 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4264+19_4264+98dup others(80): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609729 | ||||||
| chr11:609739 | C | CCCACCGA others(73): Show |
5 | a0001c0001t0001g0148 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | NA18948.hp2 NA18963.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.4264+40_4264+119du others(81): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609739 | ||||||
| chr11:609760 | A | AGTGAGTA others(113): Show |
2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.4264+128_4264+129i others(122): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609760 | ||||||
| chr11:609760 | A | C | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+40A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609760 | |||||||
| chr11:609760 | AGTGAGTA others(73): Show |
A | 1 | a0007c0012t0003g0068 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4264+48_4264+127de others(81): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609760 | ||||||
| chr11:609768 | A | G | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+48A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609768 | |||||||
| chr11:609769 | G | T | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+49G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609769 | |||||||
| chr11:609774 | T | C | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+54T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609774 | |||||||
| chr11:609782 | G | A | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+62G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609782 | |||||||
| chr11:609782 | GCCGAGGA others(33): Show |
G | 21 | a0002c0002t0001g0060 a0002c0002t0001g0193 a0002c0002t0001g0245 others(18): Show |
22 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.4264+88_4264+127de others(41): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609782 | ||||||
| chr11:609800 | C | A | 1 | a0013c0022t0002g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+80C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609800 | |||||||
| chr11:609808 | A | G | 3 | a0003c0004t0003g0189 a0003c0004t0003g0221 a0003c0004t0003g0268 |
3 | HG01346.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4264+88A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609808 | |||||||
| chr11:609822 | A | ACCGAGGA others(33): Show |
3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4264+138_4264+139i others(42): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609822 | ||||||
| chr11:609888 | T | C | 98 | a0001c0001t0001g0150 a0001c0001t0001g0206 a0001c0001t0001g0258 others(95): Show |
100 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.4264+168T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609888 | |||||||
| chr11:609930 | G | A | 1 | a0015c0036t0001g0111 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4264+210G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609930 | |||||||
| chr11:610124 | T | C | 1 | a0005c0007t0001g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4265-72T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 610124 | |||||||
| chr11:610448 | G | A | 1 | a0004c0005t0002g0033 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4417-53G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 15/17 | chr11 | 610448 | |||||||
| chr11:610450 | A | G | 2 | a0005c0007t0001g0128 a0019c0028t0001g0130 |
2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4417-51A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 15/17 | chr11 | 610450 | |||||||
| chr11:610840 | C | T | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4677+79C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 16/17 | chr11 | 610840 | |||||||
| chr11:611132 | G | A | 2 | a0016c0029t0001g0216 a0017c0038t0001g0180 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.4806+50G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611132 | |||||||
| chr11:611138 | G | A | 3 | a0012c0016t0001g0070 a0012c0016t0001g0088 a0018c0037t0001g0126 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4806+56G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611138 | |||||||
| chr11:611184 | G | A | 3 | a0001c0006t0002g0020 a0001c0006t0002g0022 a0001c0006t0002g0038 |
3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4806+102G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611184 | |||||||
| chr11:611256 | C | A | 1 | a0002c0002t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4806+174C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611256 | |||||||
| chr11:611419 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4807-215G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611419 | |||||||
| chr11:611499 | C | T | 1 | a0003c0004t0003g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4807-135C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611499 | |||||||
| chr11:611503 | G | A | 82 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(79): Show |
85 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.4807-131G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611503 | |||||||
| chr11:611513 | G | A | 1 | a0003c0004t0003g0006 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4807-121G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611513 | |||||||
| chr11:611531 | G | A | 59 | a0001c0003t0002g0015 a0001c0003t0002g0016 a0001c0003t0002g0018 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.4807-103G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611531 | |||||||
| chr11:611558 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4807-76C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611558 | |||||||
| chr11:611617 | T | C | 6 | a0003c0008t0004g0081 a0003c0008t0004g0082 a0003c0008t0004g0122 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4807-17T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611617 |