Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54919 |
| ensemblid | ENSG00000164818.16 |
| hgncid | 26013 |
| symbol | DNAAF5 |
| name | dynein axonemal assembly factor 5 |
| refseq_nuc | NM_017802.4 |
| refseq_prot | NP_060272.3 |
| ensembl_nuc | ENST00000297440.11 |
| ensembl_prot | ENSP00000297440.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 726699 |
| end | 786475 |
| strand | + |
| ver | v1.2 |
| region | chr7:726699-786475 |
| region5000 | chr7:721699-791475 |
| regionname0 | DNAAF5_chr7_726699_786475 |
| regionname5000 | DNAAF5_chr7_721699_791475 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 855 | 152 | 27 | 27 | 75 | 6 | 15 | 57 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0002 | 0/0 | 855 | 106 | 31 | 22 | 36 | 5 | 12 | 26 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0003 | 0/0 | 855 | 100 | 29 | 20 | 32 | 1 | 18 | 25 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0004 | 0/0 | 855 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0005 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0006 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0007 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0008 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0009 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0010 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0011 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0012 | 0/0 | 855 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0013 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAAPG others(850): Show |
chr7 | 721699 | 791475 |
| a0014 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0015 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0016 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| a0017 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | MAALG others(850): Show |
chr7 | 721699 | 791475 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2565 | 121 | 21 | 16 | 74 | 3 | 5 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0001c0004 | 0/0 | 2565 | 28 | 4 | 11 | 0 | 3 | 10 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0001c0016 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0001c0019 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0001c0024 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0002c0002 | 0/0 | 2565 | 100 | 29 | 21 | 33 | 5 | 12 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0002c0008 | 0/0 | 2565 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0002c0017 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0002c0022 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0002c0025 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0002c0026 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0003c0003 | 0/0 | 2565 | 84 | 14 | 19 | 32 | 1 | 18 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0003c0005 | 0/0 | 2565 | 14 | 14 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0003c0010 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0003c0012 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0004c0006 | 0/0 | 2565 | 6 | 0 | 0 | 6 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0005c0007 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0006c0011 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0007c0013 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0008c0023 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0009c0015 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0010c0020 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0011c0018 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0012c0021 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0013c0009 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0014c0014 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0015c0027 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0016c0028 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 | ||
| a0017c0029 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | ATGGC others(2560): Show |
chr7 | 721699 | 791475 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 3412 | 77 | 14 | 16 | 38 | 3 | 4 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0001t0003 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0001t0004 | 0/0 | 3412 | 31 | 6 | 0 | 25 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0001t0006 | 0/0 | 3412 | 11 | 0 | 0 | 11 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0001t0014 | 0/0 | 3412 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0004t0001 | 0/0 | 3412 | 28 | 4 | 11 | 0 | 3 | 10 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0016t0012 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0019t0004 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0001c0024t0011 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0002t0001 | 0/0 | 3412 | 93 | 26 | 20 | 30 | 5 | 12 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0002t0003 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0002t0009 | 0/0 | 3412 | 3 | 3 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0002t0013 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0002t0015 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0002t0016 | 0/0 | 3412 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0008t0001 | 0/0 | 3412 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0017t0001 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0022t0001 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0025t0001 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0002c0026t0001 | 0/0 | 3412 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0003t0001 | 0/0 | 3412 | 3 | 3 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0003t0003 | 0/0 | 3412 | 67 | 4 | 16 | 28 | 1 | 18 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0003t0004 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0003t0005 | 0/0 | 3412 | 2 | 1 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0003t0007 | 0/0 | 3412 | 7 | 5 | 2 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0003t0008 | 0/0 | 3412 | 4 | 0 | 0 | 4 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0005t0005 | 0/0 | 3412 | 14 | 14 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0010t0005 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0003c0012t0004 | 0/0 | 3412 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0004c0006t0001 | 0/0 | 3412 | 6 | 0 | 0 | 6 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0005c0007t0001 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0005c0007t0003 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0006c0011t0001 | 0/0 | 3412 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0007c0013t0001 | 0/0 | 3412 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0008c0023t0001 | 0/0 | 3412 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0009c0015t0003 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0010c0020t0001 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0011c0018t0010 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0012c0021t0002 | 0/0 | 3412 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0013c0009t0002 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0014c0014t0001 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0015c0027t0003 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0016c0028t0004 | 0/0 | 3412 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| a0017c0029t0010 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | AGTGA others(3407): Show |
chr7 | 721699 | 791475 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0001t0014g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0016t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0019t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0001c0024t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0015g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0002t0016g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0008t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0008t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0017t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0022t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0025t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0002c0026t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0003t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0005t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0010t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0003c0012t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0004c0006t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0004c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0004c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0004c0006t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0005c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0005c0007t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0006c0011t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0007c0013t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0008c0023t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0009c0015t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0010c0020t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0011c0018t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0012c0021t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0013c0009t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0014c0014t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0015c0027t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0016c0028t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| a0017c0029t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0054 | EUR | GBR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0244 | EUR | GBR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0042 | EUR | GBR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0264 | EUR | FIN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00323 | hp2 | a0003 | c0003 | t0003 | g0133 | EUR | FIN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00544 | hp2 | a0004 | c0006 | t0001 | g0221 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00558 | hp1 | a0003 | c0003 | t0008 | g0100 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | CHS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00639 | hp1 | a0003 | c0003 | t0007 | g0102 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00639 | hp2 | a0003 | c0003 | t0003 | g0001 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00642 | hp2 | a0003 | c0003 | t0003 | g0132 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00735 | hp2 | a0003 | c0003 | t0003 | g0001 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0052 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00741 | hp1 | a0006 | c0011 | t0001 | g0310 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01069 | hp2 | a0003 | c0003 | t0003 | g0001 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0040 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01074 | hp2 | a0003 | c0003 | t0003 | g0193 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01099 | hp2 | a0003 | c0003 | t0007 | g0101 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0115 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01109 | hp1 | a0007 | c0013 | t0001 | g0226 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01168 | hp2 | a0003 | c0003 | t0003 | g0019 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01169 | hp1 | a0003 | c0003 | t0003 | g0019 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0049 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01175 | hp1 | a0008 | c0023 | t0001 | g0284 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0051 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01192 | hp2 | a0002 | c0002 | t0016 | g0251 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01243 | hp2 | a0003 | c0003 | t0005 | g0256 | AMR | PUR | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0039 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0046 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0282 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0214 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0236 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0057 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01358 | hp2 | a0003 | c0003 | t0003 | g0134 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01433 | hp2 | a0003 | c0003 | t0003 | g0124 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0280 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01496 | hp2 | a0003 | c0012 | t0004 | g0056 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0043 | EUR | IBS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0238 | EUR | IBS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0055 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01891 | hp1 | a0003 | c0003 | t0004 | g0109 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01928 | hp2 | a0003 | c0003 | t0003 | g0125 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01943 | hp1 | a0003 | c0003 | t0003 | g0001 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01978 | hp1 | a0002 | c0026 | t0001 | g0211 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01978 | hp2 | a0003 | c0003 | t0003 | g0151 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01981 | hp1 | a0003 | c0003 | t0003 | g0128 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02027 | hp1 | a0009 | c0015 | t0003 | g0181 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0272 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02040 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02055 | hp1 | a0003 | c0005 | t0005 | g0255 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02056 | hp1 | a0003 | c0003 | t0003 | g0144 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02071 | hp1 | a0003 | c0003 | t0003 | g0022 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02080 | hp1 | a0002 | c0022 | t0001 | g0304 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02080 | hp2 | a0003 | c0003 | t0003 | g0022 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02083 | hp2 | a0003 | c0003 | t0003 | g0127 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02145 | hp1 | a0003 | c0003 | t0007 | g0161 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02145 | hp2 | a0003 | c0005 | t0005 | g0301 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | CDX | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | CDX | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | CDX | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | CDX | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02257 | hp2 | a0003 | c0005 | t0005 | g0219 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02258 | hp1 | a0003 | c0005 | t0005 | g0216 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02258 | hp2 | a0010 | c0020 | t0001 | g0011 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02273 | hp1 | a0003 | c0003 | t0003 | g0123 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02280 | hp2 | a0011 | c0018 | t0010 | g0120 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02602 | hp1 | a0001 | c0001 | t0014 | g0250 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02602 | hp2 | a0003 | c0003 | t0003 | g0117 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0037 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0111 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02622 | hp1 | a0003 | c0005 | t0005 | g0291 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02622 | hp2 | a0003 | c0003 | t0007 | g0232 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02630 | hp1 | a0003 | c0005 | t0005 | g0210 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02630 | hp2 | a0005 | c0007 | t0003 | g0142 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0060 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02647 | hp2 | a0001 | c0024 | t0011 | g0041 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0036 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02698 | hp2 | a0003 | c0003 | t0003 | g0140 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0116 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0044 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02738 | hp2 | a0003 | c0003 | t0003 | g0112 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02886 | hp1 | a0002 | c0002 | t0009 | g0299 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02895 | hp1 | a0002 | c0002 | t0009 | g0295 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02895 | hp2 | a0003 | c0005 | t0005 | g0287 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02897 | hp2 | a0002 | c0002 | t0009 | g0204 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02922 | hp1 | a0003 | c0003 | t0003 | g0190 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02965 | hp1 | a0003 | c0005 | t0005 | g0209 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02970 | hp2 | a0003 | c0005 | t0005 | g0258 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0137 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03017 | hp2 | a0003 | c0003 | t0003 | g0130 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03041 | hp2 | a0003 | c0003 | t0007 | g0231 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03130 | hp2 | a0002 | c0017 | t0001 | g0302 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03139 | hp2 | a0003 | c0005 | t0005 | g0259 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03225 | hp1 | a0003 | c0005 | t0005 | g0257 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03225 | hp2 | a0005 | c0007 | t0001 | g0152 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0110 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0192 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03486 | hp1 | a0003 | c0003 | t0007 | g0118 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0020 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0050 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03491 | hp1 | a0003 | c0003 | t0003 | g0007 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0004 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03492 | hp2 | a0003 | c0003 | t0003 | g0007 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03516 | hp1 | a0003 | c0003 | t0003 | g0191 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03516 | hp2 | a0003 | c0010 | t0005 | g0260 | AFR | ESN | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03579 | hp2 | a0003 | c0003 | t0005 | g0334 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0034 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03669 | hp2 | a0003 | c0003 | t0003 | g0150 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0048 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0025 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03704 | hp1 | a0003 | c0003 | t0003 | g0145 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03704 | hp2 | a0003 | c0003 | t0003 | g0146 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03710 | hp2 | a0003 | c0003 | t0003 | g0138 | SAS | PJL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0020 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0227 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0316 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0224 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03942 | hp2 | a0003 | c0003 | t0003 | g0139 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04115 | hp1 | a0003 | c0003 | t0003 | g0131 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04184 | hp2 | a0012 | c0021 | t0002 | g0327 | SAS | BEB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0045 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0053 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0035 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0031 | SAS | STU | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18522 | hp1 | a0002 | c0025 | t0001 | g0312 | AFR | YRI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | YRI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | CHB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | CHB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18747 | hp2 | a0013 | c0009 | t0002 | g0029 | EAS | CHB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0148 | AFR | YRI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | YRI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18944 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0059 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18951 | hp1 | a0002 | c0008 | t0001 | g0277 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18951 | hp2 | a0003 | c0003 | t0003 | g0143 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18959 | hp1 | a0003 | c0003 | t0008 | g0155 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18962 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18964 | hp2 | a0004 | c0006 | t0001 | g0309 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18966 | hp1 | a0014 | c0014 | t0001 | g0194 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18966 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18971 | hp1 | a0003 | c0003 | t0003 | g0147 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18973 | hp2 | a0003 | c0003 | t0003 | g0179 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18979 | hp2 | a0003 | c0003 | t0003 | g0135 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18980 | hp2 | a0002 | c0002 | t0015 | g0303 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18981 | hp1 | a0003 | c0003 | t0003 | g0129 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18983 | hp2 | a0004 | c0006 | t0001 | g0010 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18986 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18989 | hp2 | a0003 | c0003 | t0003 | g0178 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18993 | hp1 | a0003 | c0003 | t0003 | g0149 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19001 | hp1 | a0003 | c0003 | t0003 | g0122 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19002 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19003 | hp1 | a0003 | c0003 | t0008 | g0154 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19005 | hp2 | a0003 | c0003 | t0003 | g0156 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0335 | AFR | LWK | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0285 | AFR | LWK | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | LWK | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | LWK | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19055 | hp1 | a0003 | c0003 | t0003 | g0114 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19057 | hp1 | a0003 | c0003 | t0003 | g0136 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19057 | hp2 | a0002 | c0008 | t0001 | g0271 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0126 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19066 | hp2 | a0004 | c0006 | t0001 | g0010 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19074 | hp1 | a0015 | c0027 | t0003 | g0141 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19077 | hp2 | a0002 | c0002 | t0013 | g0199 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19079 | hp2 | a0003 | c0003 | t0008 | g0180 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19081 | hp1 | a0003 | c0003 | t0003 | g0113 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19082 | hp1 | a0003 | c0003 | t0003 | g0153 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19082 | hp2 | a0004 | c0006 | t0001 | g0010 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19086 | hp1 | a0016 | c0028 | t0004 | g0173 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19090 | hp1 | a0004 | c0006 | t0001 | g0220 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19240 | hp1 | a0017 | c0029 | t0010 | g0119 | AFR | YRI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20129 | hp1 | a0003 | c0005 | t0005 | g0290 | AFR | ASW | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | ASW | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0242 | EUR | TSI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | TSI | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0188 | SAS | GIH | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | GIH | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01123 | hp1 | a0003 | c0003 | t0003 | g0007 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0047 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02559 | hp1 | a0003 | c0005 | t0005 | g0228 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03471 | hp1 | a0001 | c0016 | t0012 | g0105 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG03471 | hp2 | a0003 | c0003 | t0007 | g0160 | AFR | MSL | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | USA | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | USA | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA18955 | hp2 | a0001 | c0019 | t0004 | g0174 | EAS | JPT | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | USA | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | USA | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| NA21309 | hp2 | a0003 | c0005 | t0005 | g0288 | AFR | LWK | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0080 | REF | REF | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0084 | REF | REF | DNAAF5_chr7_721699_791475 | DNAAF5 | chr7 | 721699 | 791475 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:726731 | T | C | 1 | a0013 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.11T>C | p.Leu4Pro | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 33/3412 | 11/2568 | 4/855 | chr7 | 726731 | |||
| chr7:726789 | G | T | 1 | a0016 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.69G>T | p.Glu23Asp | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 91/3412 | 69/2568 | 23/855 | chr7 | 726789 | |||
| chr7:727105 | G | C | 1 | a0006 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.385G>C | p.Val129Leu | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 407/3412 | 385/2568 | 129/855 | chr7 | 727105 | |||
| chr7:727112 | C | G | 1 | a0015 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.392C>G | p.Ala131Gly | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 414/3412 | 392/2568 | 131/855 | chr7 | 727112 | |||
| chr7:740825 | C | T | 1 | a0004 | 6 | HG00544.hp2 NA18964.hp2 NA18983.hp2 others(3): Show |
missense_variant | MODERATE | c.787C>T | p.Arg263Trp | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/13 | 809/3412 | 787/2568 | 263/855 | chr7 | 740825 | |||
| chr7:754595 | G | A | 1 | a0007 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1031G>A | p.Arg344His | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/13 | 1053/3412 | 1031/2568 | 344/855 | chr7 | 754595 | |||
| chr7:754613 | G | A | 1 | a0005 | 2 | HG02630.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.1049G>A | p.Arg350Gln | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/13 | 1071/3412 | 1049/2568 | 350/855 | chr7 | 754613 | |||
| chr7:754627 | A | G | 1 | a0008 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1063A>G | p.Arg355Gly | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/13 | 1085/3412 | 1063/2568 | 355/855 | chr7 | 754627 | |||
| chr7:756794 | G | A | 1 | a0014 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.1270G>A | p.Ala424Thr | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1292/3412 | 1270/2568 | 424/855 | chr7 | 756794 | |||
| chr7:756918 | G | A | 1 | a0009 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1394G>A | p.Arg465Gln | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1416/3412 | 1394/2568 | 465/855 | chr7 | 756918 | |||
| chr7:756950 | G | T | 1 | a0012 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1426G>T | p.Ala476Ser | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1448/3412 | 1426/2568 | 476/855 | chr7 | 756950 | |||
| chr7:756974 | A | G | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1450A>G | p.Ile484Val | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1472/3412 | 1450/2568 | 484/855 | chr7 | 756974 | |||
| chr7:763869 | C | T | 1 | a0017 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1678C>T | p.Arg560Cys | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/13 | 1700/3412 | 1678/2568 | 560/855 | chr7 | 763869 | |||
| chr7:770503 | G | A | 1 | a0008 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1816G>A | p.Val606Met | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/13 | 1838/3412 | 1816/2568 | 606/855 | chr7 | 770503 | |||
| chr7:770582 | T | C | 7 | a0002 a0004 a0006 others(4): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
missense_variant | MODERATE | c.1895T>C | p.Val632Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/13 | 1917/3412 | 1895/2568 | 632/855 | chr7 | 770582 | |||
| chr7:775151 | G | A | 11 | a0002 a0003 a0004 others(8): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
missense_variant | MODERATE | c.2228G>A | p.Arg743Lys | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/13 | 2250/3412 | 2228/2568 | 743/855 | chr7 | 775151 | |||
| chr7:785649 | A | G | 2 | a0011 a0017 |
2 | HG02280.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.2564A>G | p.Gln855Arg | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 2586/3412 | 2564/2568 | 855/855 | chr7 | 785649 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:726747 | C | T | 1 | a0017c0029 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.27C>T | p.Ala9Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 49/3412 | 27/2568 | 9/855 | chr7 | 726747 | |||
| chr7:726792 | G | A | 2 | a0003c0005 a0003c0010 |
15 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
synonymous_variant | LOW | c.72G>A | p.Ala24Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 94/3412 | 72/2568 | 24/855 | chr7 | 726792 | |||
| chr7:727176 | C | G | 1 | a0002c0026 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.456C>G | p.Ala152Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 478/3412 | 456/2568 | 152/855 | chr7 | 727176 | |||
| chr7:727197 | G | A | 1 | a0017c0029 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.477G>A | p.Ala159Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/13 | 499/3412 | 477/2568 | 159/855 | chr7 | 727197 | |||
| chr7:729844 | G | T | 1 | a0002c0025 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.777G>T | p.Pro259Pro | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/13 | 799/3412 | 777/2568 | 259/855 | chr7 | 729844 | |||
| chr7:740830 | G | A | 1 | a0003c0012 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.792G>A | p.Ala264Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/13 | 814/3412 | 792/2568 | 264/855 | chr7 | 740830 | |||
| chr7:741374 | C | T | 1 | a0003c0010 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.933C>T | p.Asp311Asp | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/13 | 955/3412 | 933/2568 | 311/855 | chr7 | 741374 | |||
| chr7:754620 | C | T | 1 | a0001c0024 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1056C>T | p.Leu352Leu | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/13 | 1078/3412 | 1056/2568 | 352/855 | chr7 | 754620 | |||
| chr7:756793 | C | T | 1 | a0001c0004 | 28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
synonymous_variant | LOW | c.1269C>T | p.Ser423Ser | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1291/3412 | 1269/2568 | 423/855 | chr7 | 756793 | |||
| chr7:756895 | C | T | 1 | a0002c0022 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1371C>T | p.Ala457Ala | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1393/3412 | 1371/2568 | 457/855 | chr7 | 756895 | |||
| chr7:756934 | G | C | 1 | a0002c0008 | 2 | NA18951.hp1 NA19057.hp2 |
synonymous_variant | LOW | c.1410G>C | p.Pro470Pro | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/13 | 1432/3412 | 1410/2568 | 470/855 | chr7 | 756934 | |||
| chr7:763817 | G | A | 1 | a0001c0016 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1626G>A | p.Thr542Thr | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/13 | 1648/3412 | 1626/2568 | 542/855 | chr7 | 763817 | |||
| chr7:770499 | C | T | 1 | a0001c0019 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.1812C>T | p.His604His | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/13 | 1834/3412 | 1812/2568 | 604/855 | chr7 | 770499 | |||
| chr7:770502 | C | G | 1 | a0003c0012 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1815C>G | p.Val605Val | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/13 | 1837/3412 | 1815/2568 | 605/855 | chr7 | 770502 | |||
| chr7:785557 | G | A | 2 | a0002c0017 a0002c0025 |
2 | HG03130.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.2472G>A | p.Leu824Leu | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 2494/3412 | 2472/2568 | 824/855 | chr7 | 785557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:785792 | A | G | 38 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(35): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*139A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 139 | chr7 | 785792 | ||||||
| chr7:785857 | G | A | 9 | a0001c0001t0003 a0002c0002t0003 a0003c0003t0003 others(6): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 204 | chr7 | 785857 | ||||||
| chr7:785893 | T | G | 1 | a0002c0002t0009 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*240T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 240 | chr7 | 785893 | ||||||
| chr7:785919 | C | T | 1 | a0002c0002t0016 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 266 | chr7 | 785919 | ||||||
| chr7:785972 | C | T | 1 | a0002c0002t0015 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 319 | chr7 | 785972 | ||||||
| chr7:786030 | A | C | 1 | a0001c0016t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 377 | chr7 | 786030 | ||||||
| chr7:786033 | A | G | 1 | a0001c0001t0014 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 380 | chr7 | 786033 | ||||||
| chr7:786149 | T | C | 31 | a0001c0001t0003 a0001c0004t0001 a0002c0002t0001 others(28): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*496T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 496 | chr7 | 786149 | ||||||
| chr7:786199 | G | A | 3 | a0003c0003t0005 a0003c0005t0005 a0003c0010t0005 |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*546G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 546 | chr7 | 786199 | ||||||
| chr7:786206 | G | A | 1 | a0003c0003t0007 | 7 | HG00639.hp1 HG01099.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*553G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 553 | chr7 | 786206 | ||||||
| chr7:786268 | G | T | 1 | a0001c0001t0006 | 11 | HG00558.hp2 HG02015.hp2 HG02071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*615G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 615 | chr7 | 786268 | ||||||
| chr7:786315 | C | T | 1 | a0003c0003t0008 | 4 | HG00558.hp1 NA18959.hp1 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*662C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 662 | chr7 | 786315 | ||||||
| chr7:786332 | A | G | 1 | a0002c0002t0013 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 679 | chr7 | 786332 | ||||||
| chr7:786403 | G | A | 2 | a0011c0018t0010 a0017c0029t0010 |
2 | HG02280.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 750 | chr7 | 786403 | ||||||
| chr7:786465 | G | A | 40 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(37): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*812G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 13/13 | 812 | chr7 | 786465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:727345 | C | A | 30 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.595+30C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727345 | |||||||
| chr7:727397 | C | A | 1 | a0001c0004t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.595+82C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727397 | |||||||
| chr7:727488 | A | C | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.595+173A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727488 | |||||||
| chr7:727498 | GC | G | 12 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0325 others(9): Show |
13 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.595+188delC | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr7 | 727498 | ||||||
| chr7:727621 | C | T | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.595+306C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727621 | |||||||
| chr7:727689 | C | T | 7 | a0001c0001t0002g0028 a0001c0001t0002g0319 a0001c0001t0002g0320 others(4): Show |
8 | NA18612.hp2 NA18955.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.595+374C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727689 | |||||||
| chr7:727697 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595+382C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727697 | |||||||
| chr7:727789 | A | G | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG03927.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.595+474A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727789 | |||||||
| chr7:727808 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.595+493C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727808 | |||||||
| chr7:727850 | C | G | 128 | a0001c0001t0002g0207 a0001c0001t0002g0306 a0001c0001t0004g0237 others(125): Show |
135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.595+535C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727850 | |||||||
| chr7:727917 | T | G | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.595+602T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 727917 | |||||||
| chr7:728099 | C | T | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.595+784C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728099 | |||||||
| chr7:728383 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.595+1068G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728383 | |||||||
| chr7:728457 | C | G | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.595+1142C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728457 | |||||||
| chr7:728473 | G | A | 1 | a0001c0001t0002g0319 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.595+1158G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728473 | |||||||
| chr7:728485 | G | A | 1 | a0003c0003t0003g0059 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.595+1170G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728485 | |||||||
| chr7:728494 | A | G | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.596-1169A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728494 | |||||||
| chr7:728505 | T | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.596-1158T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728505 | |||||||
| chr7:728598 | C | T | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.596-1065C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728598 | |||||||
| chr7:728615 | C | G | 2 | a0003c0003t0003g0190 a0003c0003t0003g0191 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.596-1048C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728615 | |||||||
| chr7:728619 | A | C | 1 | a0001c0001t0002g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.596-1044A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728619 | |||||||
| chr7:728649 | C | T | 2 | a0003c0003t0003g0190 a0003c0003t0003g0191 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.596-1014C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728649 | |||||||
| chr7:728680 | T | C | 1 | a0003c0003t0003g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.596-983T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728680 | |||||||
| chr7:728740 | G | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.596-923G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728740 | |||||||
| chr7:728744 | T | C | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.596-919T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728744 | |||||||
| chr7:728841 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0189 |
3 | HG03491.hp2 HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.596-822G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728841 | |||||||
| chr7:728855 | C | G | 1 | a0002c0025t0001g0312 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.596-808C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728855 | |||||||
| chr7:728918 | C | T | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.596-745C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728918 | |||||||
| chr7:728938 | A | G | 1 | a0003c0003t0003g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.596-725A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 728938 | |||||||
| chr7:728995 | C | CT | 131 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0099 others(128): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.596-649dupT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr7 | 728995 | ||||||
| chr7:728995 | C | CTT | 110 | a0001c0001t0002g0003 a0001c0001t0002g0162 a0001c0001t0003g0318 others(107): Show |
131 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.596-650_596-649dup others(2): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr7 | 728995 | ||||||
| chr7:728995 | C | CTTT | 20 | a0001c0001t0002g0183 a0001c0001t0004g0184 a0001c0001t0004g0185 others(17): Show |
20 | HG00099.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.596-651_596-649dup others(3): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr7 | 728995 | ||||||
| chr7:729142 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.596-521G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729142 | |||||||
| chr7:729298 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(32): Show |
40 | HG00558.hp2 HG02015.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.596-365G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729298 | |||||||
| chr7:729406 | G | A | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.596-257G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729406 | |||||||
| chr7:729518 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596-145G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729518 | |||||||
| chr7:729547 | A | G | 270 | a0001c0001t0002g0003 a0001c0001t0002g0092 a0001c0001t0002g0103 others(267): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.596-116A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729547 | |||||||
| chr7:729555 | A | G | 29 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0034 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.596-108A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729555 | |||||||
| chr7:729559 | G | T | 29 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0034 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.596-104G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 1/12 | chr7 | 729559 | |||||||
| chr7:729903 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.780+56C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 729903 | |||||||
| chr7:730013 | T | C | 1 | a0002c0002t0001g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.780+166T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730013 | |||||||
| chr7:730014 | A | G | 3 | a0001c0004t0001g0052 a0001c0004t0001g0053 a0001c0004t0001g0055 |
3 | HG00738.hp1 HG01884.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.780+167A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730014 | |||||||
| chr7:730081 | T | C | 1 | a0001c0004t0001g0034 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.780+234T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730081 | |||||||
| chr7:730082 | G | A | 2 | a0001c0004t0001g0035 a0001c0004t0001g0036 |
2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.780+235G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730082 | |||||||
| chr7:730095 | C | A | 2 | a0003c0005t0005g0209 a0003c0005t0005g0210 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.780+248C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730095 | |||||||
| chr7:730358 | G | A | 3 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0039 |
3 | HG01255.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.780+511G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730358 | |||||||
| chr7:730365 | G | A | 1 | a0002c0026t0001g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.780+518G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730365 | |||||||
| chr7:730465 | CAT | C | 2 | a0004c0006t0001g0010 a0004c0006t0001g0309 |
4 | NA18964.hp2 NA18983.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+619_780+620del others(2): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730465 | |||||||
| chr7:730626 | G | A | 2 | a0003c0003t0003g0110 a0003c0003t0004g0109 |
2 | HG01891.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.780+779G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730626 | |||||||
| chr7:730645 | G | A | 2 | a0002c0002t0001g0212 a0003c0003t0001g0111 |
2 | HG02615.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.780+798G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730645 | |||||||
| chr7:730768 | C | G | 1 | a0004c0006t0001g0309 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.780+921C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730768 | |||||||
| chr7:730810 | AC | A | 186 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(183): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.780+969delC | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 730810 | ||||||
| chr7:730816 | C | T | 3 | a0001c0001t0002g0306 a0002c0002t0001g0307 a0002c0002t0001g0308 |
3 | NA18945.hp1 NA18997.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.780+969C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730816 | |||||||
| chr7:730856 | C | T | 32 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(29): Show |
34 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.780+1009C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730856 | |||||||
| chr7:730980 | G | C | 67 | a0001c0004t0001g0115 a0002c0002t0001g0121 a0002c0002t0001g0182 others(64): Show |
81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.780+1133G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730980 | |||||||
| chr7:730984 | G | A | 2 | a0002c0002t0001g0011 a0010c0020t0001g0011 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.780+1137G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 730984 | |||||||
| chr7:731035 | G | A | 1 | a0003c0003t0003g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.780+1188G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731035 | |||||||
| chr7:731085 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.780+1238G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731085 | |||||||
| chr7:731409 | G | A | 1 | a0001c0001t0002g0320 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.780+1562G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731409 | |||||||
| chr7:731432 | C | T | 1 | a0003c0003t0003g0156 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.780+1585C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731432 | |||||||
| chr7:731450 | A | G | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.780+1603A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731450 | |||||||
| chr7:731651 | T | G | 2 | a0003c0003t0003g0113 a0003c0003t0003g0114 |
2 | NA19055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.780+1804T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731651 | |||||||
| chr7:731666 | C | T | 24 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(21): Show |
26 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(23): Show |
intron_variant | MODIFIER | c.780+1819C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731666 | |||||||
| chr7:731822 | G | T | 24 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(21): Show |
26 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(23): Show |
intron_variant | MODIFIER | c.780+1975G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 731822 | |||||||
| chr7:732006 | C | G | 3 | a0003c0003t0008g0100 a0003c0003t0008g0154 a0003c0003t0008g0155 |
3 | HG00558.hp1 NA18959.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.780+2159C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732006 | |||||||
| chr7:732136 | C | T | 1 | a0002c0002t0001g0305 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.780+2289C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732136 | |||||||
| chr7:732209 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.780+2362G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732209 | |||||||
| chr7:732212 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.780+2365A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732212 | |||||||
| chr7:732306 | G | A | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.780+2459G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732306 | |||||||
| chr7:732336 | T | A | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.780+2489T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732336 | |||||||
| chr7:732388 | G | A | 129 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(126): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.780+2541G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732388 | |||||||
| chr7:732403 | C | T | 1 | a0003c0003t0003g0153 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.780+2556C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732403 | |||||||
| chr7:732435 | C | T | 1 | a0002c0022t0001g0304 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.780+2588C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732435 | |||||||
| chr7:732533 | G | A | 1 | a0003c0003t0003g0214 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.780+2686G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732533 | |||||||
| chr7:732537 | G | A | 265 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(262): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.780+2690G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732537 | |||||||
| chr7:732541 | C | T | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.780+2694C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732541 | |||||||
| chr7:732563 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.780+2716G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732563 | |||||||
| chr7:732937 | A | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.780+3090A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732937 | |||||||
| chr7:732992 | G | T | 2 | a0002c0002t0001g0182 a0005c0007t0001g0152 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.780+3145G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 732992 | |||||||
| chr7:733284 | G | T | 1 | a0001c0001t0002g0063 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.780+3437G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733284 | |||||||
| chr7:733329 | T | C | 1 | a0001c0004t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.780+3482T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733329 | |||||||
| chr7:733432 | A | G | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.780+3585A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733432 | |||||||
| chr7:733488 | A | T | 1 | a0003c0003t0003g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.780+3641A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733488 | |||||||
| chr7:733539 | C | T | 2 | a0001c0001t0006g0076 a0001c0001t0006g0077 |
2 | HG00558.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.780+3692C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733539 | |||||||
| chr7:733618 | T | C | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.780+3771T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733618 | |||||||
| chr7:733641 | T | C | 266 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(263): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.780+3794T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733641 | |||||||
| chr7:733643 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.780+3796C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733643 | |||||||
| chr7:733754 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.780+3907A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733754 | |||||||
| chr7:733786 | G | A | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.780+3939G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733786 | |||||||
| chr7:733791 | G | T | 1 | a0001c0001t0002g0333 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.780+3944G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733791 | |||||||
| chr7:733792 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.780+3945C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733792 | |||||||
| chr7:733805 | A | T | 1 | a0002c0002t0015g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.780+3958A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733805 | |||||||
| chr7:733807 | T | C | 2 | a0003c0003t0003g0116 a0003c0003t0003g0117 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.780+3960T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733807 | |||||||
| chr7:733809 | T | C | 1 | a0003c0005t0005g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.780+3962T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 733809 | |||||||
| chr7:734001 | G | T | 1 | a0001c0004t0001g0051 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.780+4154G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734001 | |||||||
| chr7:734107 | A | G | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.780+4260A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734107 | |||||||
| chr7:734165 | C | A | 30 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.780+4318C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734165 | |||||||
| chr7:734221 | G | A | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.780+4374G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734221 | |||||||
| chr7:734356 | C | T | 1 | a0003c0003t0003g0150 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.780+4509C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734356 | |||||||
| chr7:734380 | C | T | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.780+4533C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734380 | |||||||
| chr7:734423 | T | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.780+4576T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734423 | |||||||
| chr7:734503 | C | T | 1 | a0003c0003t0003g0149 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.780+4656C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734503 | |||||||
| chr7:734711 | C | T | 2 | a0004c0006t0001g0010 a0004c0006t0001g0309 |
4 | NA18964.hp2 NA18983.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+4864C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734711 | |||||||
| chr7:734735 | G | A | 1 | a0014c0014t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.780+4888G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734735 | |||||||
| chr7:734865 | C | G | 1 | a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.780+5018C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 734865 | |||||||
| chr7:735006 | G | A | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.780+5159G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735006 | |||||||
| chr7:735039 | G | A | 9 | a0001c0001t0004g0023 a0001c0001t0004g0106 a0001c0001t0004g0163 others(6): Show |
10 | NA18612.hp1 NA18939.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+5192G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735039 | |||||||
| chr7:735065 | T | C | 1 | a0002c0002t0001g0218 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.780+5218T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735065 | |||||||
| chr7:735137 | C | T | 65 | a0001c0004t0001g0115 a0002c0002t0001g0121 a0002c0002t0001g0182 others(62): Show |
79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.780+5290C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735137 | |||||||
| chr7:735179 | T | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.780+5332T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735179 | |||||||
| chr7:735208 | A | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0183 |
2 | HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.780+5361A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735208 | |||||||
| chr7:735210 | G | A | 1 | a0003c0005t0005g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780+5363G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735210 | |||||||
| chr7:735222 | T | C | 265 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(262): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.780+5375T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735222 | |||||||
| chr7:735230 | AG | A | 12 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(9): Show |
13 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.780+5384delG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735230 | |||||||
| chr7:735290 | C | T | 1 | a0002c0017t0001g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.780+5443C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735290 | |||||||
| chr7:735317 | AGTTCATG others(122): Show |
A | 1 | a0002c0002t0001g0205 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.781-5482_781-5354d others(2): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 735317 | ||||||
| chr7:735331 | C | G | 30 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.780+5484C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735331 | |||||||
| chr7:735338 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.781-5481C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735338 | |||||||
| chr7:735355 | G | C | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781-5464G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735355 | |||||||
| chr7:735438 | G | A | 152 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(149): Show |
161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.781-5381G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735438 | |||||||
| chr7:735452 | TGGTGTAG others(8): Show |
T | 2 | a0002c0017t0001g0302 a0002c0025t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.781-5353_781-5339d others(17): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 735452 | ||||||
| chr7:735465 | C | G | 1 | a0003c0003t0003g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.781-5354C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735465 | |||||||
| chr7:735480 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0063 a0001c0001t0002g0075 others(1): Show |
5 | HG02015.hp1 HG02135.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-5339C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735480 | |||||||
| chr7:735510 | G | C | 264 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(261): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.781-5309G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735510 | |||||||
| chr7:735510 | G | T | 1 | a0003c0003t0003g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.781-5309G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735510 | |||||||
| chr7:735515 | T | A | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781-5304T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735515 | |||||||
| chr7:735524 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.781-5295C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735524 | |||||||
| chr7:735528 | T | G | 1 | a0002c0002t0001g0205 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.781-5291T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735528 | |||||||
| chr7:735652 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781-5167C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735652 | |||||||
| chr7:735658 | C | G | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.781-5161C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735658 | |||||||
| chr7:735758 | G | T | 154 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(151): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.781-5061G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735758 | |||||||
| chr7:735822 | G | C | 2 | a0004c0006t0001g0220 a0004c0006t0001g0221 |
2 | HG00544.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.781-4997G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 735822 | |||||||
| chr7:736027 | C | T | 65 | a0001c0004t0001g0115 a0002c0002t0001g0121 a0002c0002t0001g0182 others(62): Show |
79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.781-4792C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736027 | |||||||
| chr7:736060 | G | A | 265 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(262): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.781-4759G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736060 | |||||||
| chr7:736133 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.781-4686C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736133 | |||||||
| chr7:736173 | G | A | 2 | a0002c0002t0001g0222 a0002c0002t0001g0223 |
2 | HG00642.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.781-4646G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736173 | |||||||
| chr7:736180 | G | C | 1 | a0002c0002t0001g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.781-4639G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736180 | |||||||
| chr7:736186 | G | C | 130 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(127): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.781-4633G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736186 | |||||||
| chr7:736442 | C | T | 1 | a0001c0004t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.781-4377C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736442 | |||||||
| chr7:736474 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781-4345A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736474 | |||||||
| chr7:736582 | C | T | 24 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(21): Show |
26 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-4237C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736582 | |||||||
| chr7:736587 | G | A | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.781-4232G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736587 | |||||||
| chr7:736613 | C | T | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.781-4206C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736613 | |||||||
| chr7:736634 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.781-4185G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736634 | |||||||
| chr7:736661 | C | T | 2 | a0003c0005t0005g0216 a0003c0005t0005g0301 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.781-4158C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736661 | |||||||
| chr7:736665 | C | G | 2 | a0004c0006t0001g0220 a0004c0006t0001g0221 |
2 | HG00544.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.781-4154C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736665 | |||||||
| chr7:736688 | G | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.781-4131G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736688 | |||||||
| chr7:736697 | C | T | 1 | a0003c0003t0003g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.781-4122C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736697 | |||||||
| chr7:736703 | A | G | 1 | a0002c0026t0001g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.781-4116A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736703 | |||||||
| chr7:736738 | G | A | 1 | a0001c0001t0006g0104 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.781-4081G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736738 | |||||||
| chr7:736762 | G | C | 9 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0197 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-4057G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736762 | |||||||
| chr7:736777 | T | G | 1 | a0001c0004t0001g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.781-4042T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736777 | |||||||
| chr7:736827 | G | A | 1 | a0007c0013t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.781-3992G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736827 | |||||||
| chr7:736847 | T | G | 1 | a0002c0002t0001g0227 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.781-3972T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736847 | |||||||
| chr7:736847 | T | TTG | 157 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(154): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.781-3960_781-3959d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 736847 | ||||||
| chr7:736849 | G | T | 1 | a0001c0001t0002g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.781-3970G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 736849 | |||||||
| chr7:736998 | AT | A | 24 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(21): Show |
26 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-3817delT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 736998 | ||||||
| chr7:737086 | A | T | 1 | a0002c0002t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.781-3733A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737086 | |||||||
| chr7:737137 | C | A | 31 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(28): Show |
33 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.781-3682C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737137 | |||||||
| chr7:737176 | A | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.781-3643A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737176 | |||||||
| chr7:737180 | C | A | 131 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(128): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.781-3639C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737180 | |||||||
| chr7:737181 | C | T | 131 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(128): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.781-3638C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737181 | |||||||
| chr7:737221 | G | A | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.781-3598G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737221 | |||||||
| chr7:737544 | G | A | 2 | a0003c0003t0001g0335 a0003c0003t0005g0334 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.781-3275G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737544 | |||||||
| chr7:737545 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.781-3274C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737545 | |||||||
| chr7:737636 | T | C | 1 | a0003c0003t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.781-3183T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737636 | |||||||
| chr7:737757 | G | T | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.781-3062G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737757 | |||||||
| chr7:737821 | C | A | 1 | a0003c0005t0005g0228 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.781-2998C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737821 | |||||||
| chr7:737887 | A | C | 7 | a0002c0002t0001g0294 a0002c0002t0001g0296 a0002c0002t0001g0297 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-2932A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737887 | |||||||
| chr7:737902 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.781-2917G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 737902 | |||||||
| chr7:738147 | G | A | 29 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.781-2672G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738147 | |||||||
| chr7:738180 | A | G | 2 | a0002c0002t0001g0292 a0002c0002t0001g0293 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.781-2639A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738180 | |||||||
| chr7:738244 | G | A | 2 | a0001c0004t0001g0035 a0001c0004t0001g0036 |
2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.781-2575G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738244 | |||||||
| chr7:738406 | G | C | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.781-2413G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738406 | |||||||
| chr7:738419 | T | A | 189 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(186): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.781-2400T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738419 | |||||||
| chr7:738582 | G | GA | 197 | a0001c0001t0002g0103 a0001c0001t0002g0207 a0001c0001t0002g0306 others(194): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.781-2228dupA | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 738582 | ||||||
| chr7:738633 | C | T | 2 | a0002c0017t0001g0302 a0002c0025t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.781-2186C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738633 | |||||||
| chr7:738730 | T | C | 1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.781-2089T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738730 | |||||||
| chr7:738833 | G | C | 1 | a0001c0004t0001g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.781-1986G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738833 | |||||||
| chr7:738841 | G | A | 1 | a0003c0005t0005g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.781-1978G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738841 | |||||||
| chr7:738878 | C | A | 1 | a0002c0002t0001g0205 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.781-1941C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 738878 | |||||||
| chr7:739031 | G | GGCCCCAT others(131): Show |
1 | a0001c0001t0002g0326 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.781-1773_781-1636d others(140): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 739031 | ||||||
| chr7:739040 | A | G | 20 | a0001c0001t0002g0016 a0001c0001t0002g0090 a0001c0001t0003g0318 others(17): Show |
22 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.781-1779A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739040 | |||||||
| chr7:739046 | CACCTGTT others(62): Show |
C | 131 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0090 others(128): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.781-1646_781-1578d others(71): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 739046 | ||||||
| chr7:739046 | CACCTGTT others(131): Show |
C | 130 | a0001c0001t0002g0320 a0001c0001t0004g0157 a0001c0001t0004g0158 others(127): Show |
149 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.781-1715_781-1578d others(2): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 739046 | ||||||
| chr7:739115 | T | C | 3 | a0003c0003t0007g0231 a0003c0003t0007g0232 a0003c0012t0004g0056 |
3 | HG01496.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.781-1704T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739115 | |||||||
| chr7:739129 | G | A | 1 | a0005c0007t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-1690G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739129 | |||||||
| chr7:739162 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.781-1657C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739162 | |||||||
| chr7:739174 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.781-1645C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739174 | |||||||
| chr7:739184 | T | C | 1 | a0003c0003t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.781-1635T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739184 | |||||||
| chr7:739240 | C | T | 1 | a0003c0003t0003g0114 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.781-1579C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739240 | |||||||
| chr7:739355 | C | A | 2 | a0003c0003t0007g0160 a0003c0003t0007g0161 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.781-1464C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739355 | |||||||
| chr7:739475 | T | G | 4 | a0001c0004t0001g0115 a0003c0003t0004g0109 a0003c0003t0007g0231 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-1344T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739475 | |||||||
| chr7:739489 | G | A | 1 | a0006c0011t0001g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.781-1330G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739489 | |||||||
| chr7:739549 | G | A | 1 | a0001c0001t0002g0016 | 2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.781-1270G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739549 | |||||||
| chr7:739566 | C | G | 1 | a0003c0003t0003g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.781-1253C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739566 | |||||||
| chr7:739572 | G | A | 1 | a0001c0001t0006g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.781-1247G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739572 | |||||||
| chr7:739574 | G | A | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-1245G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739574 | |||||||
| chr7:739584 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.781-1235G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739584 | |||||||
| chr7:739591 | G | A | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.781-1228G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739591 | |||||||
| chr7:739605 | G | A | 2 | a0001c0001t0002g0079 a0002c0002t0001g0236 |
2 | HG01346.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.781-1214G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739605 | |||||||
| chr7:739616 | C | T | 1 | a0003c0003t0003g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.781-1203C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739616 | |||||||
| chr7:739617 | C | T | 1 | a0002c0002t0001g0308 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.781-1202C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739617 | |||||||
| chr7:739639 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781-1180C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739639 | |||||||
| chr7:739650 | T | C | 1 | a0001c0001t0004g0185 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.781-1169T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739650 | |||||||
| chr7:739680 | G | A | 1 | a0002c0002t0001g0294 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781-1139G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739680 | |||||||
| chr7:739826 | C | T | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.781-993C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739826 | |||||||
| chr7:739830 | G | A | 1 | a0003c0003t0003g0019 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.781-989G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739830 | |||||||
| chr7:739831 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.781-988C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739831 | |||||||
| chr7:739832 | G | A | 1 | a0001c0001t0006g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.781-987G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739832 | |||||||
| chr7:739833 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0099 |
3 | HG01175.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.781-986G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739833 | |||||||
| chr7:739868 | C | T | 33 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(30): Show |
35 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.781-951C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739868 | |||||||
| chr7:739890 | C | T | 59 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(56): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.781-929C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739890 | |||||||
| chr7:739907 | C | T | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781-912C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739907 | |||||||
| chr7:739921 | C | T | 2 | a0003c0003t0001g0111 a0005c0007t0001g0152 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.781-898C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 739921 | |||||||
| chr7:740016 | A | G | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.781-803A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740016 | |||||||
| chr7:740093 | A | C | 236 | a0001c0001t0002g0103 a0001c0001t0003g0318 a0001c0001t0004g0157 others(233): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.781-726A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740093 | |||||||
| chr7:740228 | T | C | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.781-591T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740228 | |||||||
| chr7:740280 | G | A | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-539G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740280 | |||||||
| chr7:740483 | C | T | 25 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(22): Show |
27 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-336C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740483 | |||||||
| chr7:740518 | A | G | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-301A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740518 | |||||||
| chr7:740537 | C | T | 1 | a0002c0002t0015g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.781-282C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740537 | |||||||
| chr7:740538 | G | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.781-281G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740538 | |||||||
| chr7:740659 | G | C | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-160G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740659 | |||||||
| chr7:740681 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.781-138G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740681 | |||||||
| chr7:740731 | G | A | 12 | a0003c0003t0003g0001 a0003c0003t0003g0123 a0003c0003t0003g0124 others(9): Show |
15 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.781-88G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740731 | |||||||
| chr7:740761 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.781-58G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740761 | |||||||
| chr7:740764 | A | G | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-55A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740764 | |||||||
| chr7:740770 | G | A | 2 | a0002c0002t0001g0292 a0002c0002t0001g0293 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.781-49G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740770 | |||||||
| chr7:740786 | A | T | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-33A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 2/12 | chr7 | 740786 | |||||||
| chr7:740991 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.905+48G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/12 | chr7 | 740991 | |||||||
| chr7:741087 | C | T | 2 | a0001c0001t0003g0318 a0003c0012t0004g0056 |
2 | HG01496.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.905+144C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/12 | chr7 | 741087 | |||||||
| chr7:741177 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.906-170G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/12 | chr7 | 741177 | |||||||
| chr7:741222 | T | G | 107 | a0001c0001t0014g0250 a0002c0002t0001g0009 a0002c0002t0001g0018 others(104): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.906-125T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/12 | chr7 | 741222 | |||||||
| chr7:741343 | T | G | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
splice_region_variant&intron_variant | LOW | c.906-4T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 3/12 | chr7 | 741343 | |||||||
| chr7:741476 | G | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1024+11G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 741476 | |||||||
| chr7:741615 | G | A | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1024+150G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 741615 | |||||||
| chr7:741627 | C | G | 1 | a0005c0007t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1024+162C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 741627 | |||||||
| chr7:741721 | C | A | 1 | a0001c0004t0001g0042 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1024+256C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 741721 | |||||||
| chr7:741775 | G | C | 220 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(217): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1024+310G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 741775 | |||||||
| chr7:741781 | TGTGCACA others(5): Show |
T | 1 | a0001c0001t0004g0187 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1024+322_1024+333d others(14): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 741781 | ||||||
| chr7:741950 | T | G | 1 | a0003c0003t0003g0126 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1024+485T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 741950 | |||||||
| chr7:742016 | G | A | 213 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(210): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1024+551G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742016 | |||||||
| chr7:742037 | C | T | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+572C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742037 | |||||||
| chr7:742117 | G | A | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1024+652G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742117 | |||||||
| chr7:742148 | C | T | 1 | a0003c0003t0007g0232 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1024+683C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742148 | |||||||
| chr7:742235 | A | T | 1 | a0001c0001t0004g0167 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1024+770A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742235 | |||||||
| chr7:742260 | A | G | 1 | a0001c0001t0006g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1024+795A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742260 | |||||||
| chr7:742292 | CATCAGAT others(11): Show |
C | 1 | a0003c0010t0005g0260 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1024+842_1024+859d others(20): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742292 | ||||||
| chr7:742361 | T | TCAAATCA others(382): Show |
22 | a0001c0001t0004g0024 a0001c0001t0004g0107 a0001c0001t0004g0108 others(19): Show |
23 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(20): Show |
intron_variant | MODIFIER | c.1024+1070_1024+107 others(393): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742361 | ||||||
| chr7:742407 | CA | C | 220 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(217): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1024+944delA | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742407 | ||||||
| chr7:742447 | T | TCATGCCC others(11): Show |
1 | a0001c0001t0002g0320 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1024+1001_1024+101 others(22): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742447 | ||||||
| chr7:742486 | C | CATGCCCA others(11): Show |
2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1038_1024+103 others(22): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742486 | ||||||
| chr7:742487 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1024+1022A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742487 | |||||||
| chr7:742516 | T | C | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1051T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742516 | |||||||
| chr7:742526 | T | C | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1061T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742526 | |||||||
| chr7:742536 | C | A | 334 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(331): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1024+1071C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742536 | |||||||
| chr7:742540 | C | A | 1 | a0005c0007t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1024+1075C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742540 | |||||||
| chr7:742562 | C | T | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1097C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742562 | |||||||
| chr7:742580 | C | CACATGCC others(27): Show |
2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1116_1024+111 others(38): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742580 | ||||||
| chr7:742586 | G | C | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1121G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742586 | |||||||
| chr7:742596 | C | T | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1131C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742596 | |||||||
| chr7:742602 | C | T | 217 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(214): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1024+1137C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742602 | |||||||
| chr7:742604 | G | C | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1139G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742604 | |||||||
| chr7:742606 | C | CGCCCAGC others(31): Show |
1 | a0002c0002t0001g0305 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1024+1195_1024+123 others(42): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742606 | ||||||
| chr7:742606 | C | CGCCCAGC others(69): Show |
104 | a0001c0001t0014g0250 a0002c0002t0001g0009 a0002c0002t0001g0018 others(101): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1024+1157_1024+123 others(80): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742606 | ||||||
| chr7:742606 | C | T | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024+1141C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742606 | |||||||
| chr7:742678 | A | G | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1024+1213A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742678 | |||||||
| chr7:742776 | C | G | 1 | a0003c0003t0007g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1024+1311C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742776 | |||||||
| chr7:742821 | CGCTCAAA others(13): Show |
C | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1024+1387_1024+140 others(24): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 742821 | ||||||
| chr7:742910 | A | G | 1 | a0001c0004t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1024+1445A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742910 | |||||||
| chr7:742963 | T | C | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+1498T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 742963 | |||||||
| chr7:743012 | G | A | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1024+1547G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743012 | |||||||
| chr7:743063 | C | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1024+1598C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743063 | |||||||
| chr7:743120 | G | A | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1024+1655G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743120 | |||||||
| chr7:743229 | A | C | 107 | a0001c0001t0014g0250 a0002c0002t0001g0009 a0002c0002t0001g0018 others(104): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1024+1764A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743229 | |||||||
| chr7:743269 | A | C | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+1804A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743269 | |||||||
| chr7:743269 | A | G | 238 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(235): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1024+1804A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743269 | |||||||
| chr7:743313 | T | A | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+1848T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743313 | |||||||
| chr7:743351 | G | A | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+1886G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743351 | |||||||
| chr7:743374 | A | AAAAC | 27 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(24): Show |
29 | HG00621.hp1 HG02132.hp1 HG03471.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024+1925_1024+192 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 743374 | ||||||
| chr7:743374 | AAAAC | A | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1024+1925_1024+192 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 743374 | ||||||
| chr7:743557 | A | AAAGC | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1024+2094_1024+209 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 743557 | ||||||
| chr7:743564 | A | C | 1 | a0001c0001t0002g0320 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1024+2099A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743564 | |||||||
| chr7:743642 | C | CT | 89 | a0001c0001t0002g0087 a0001c0001t0002g0103 a0001c0001t0004g0313 others(86): Show |
105 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1024+2196dupT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 743642 | ||||||
| chr7:743679 | T | C | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1024+2214T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743679 | |||||||
| chr7:743714 | G | A | 1 | a0017c0029t0010g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1024+2249G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743714 | |||||||
| chr7:743731 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1024+2266A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743731 | |||||||
| chr7:743800 | A | G | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+2335A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743800 | |||||||
| chr7:743801 | C | T | 60 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1024+2336C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 743801 | |||||||
| chr7:744160 | A | G | 2 | a0001c0001t0002g0072 a0003c0003t0003g0146 |
2 | HG03704.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1024+2695A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744160 | |||||||
| chr7:744164 | C | T | 218 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(215): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1024+2699C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744164 | |||||||
| chr7:744186 | G | A | 3 | a0001c0001t0006g0065 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02015.hp2 HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1024+2721G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744186 | |||||||
| chr7:744208 | C | T | 29 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(26): Show |
30 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1024+2743C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744208 | |||||||
| chr7:744392 | A | G | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1024+2927A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744392 | |||||||
| chr7:744402 | A | G | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1024+2937A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744402 | |||||||
| chr7:744464 | A | T | 1 | a0002c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1024+2999A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744464 | |||||||
| chr7:744490 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1024+3025G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744490 | |||||||
| chr7:744547 | G | GCAGCCAA others(3): Show |
9 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0197 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024+3082_1024+308 others(14): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744547 | |||||||
| chr7:744549 | A | C | 9 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0197 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024+3084A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744549 | |||||||
| chr7:744599 | G | T | 1 | a0001c0004t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1024+3134G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744599 | |||||||
| chr7:744663 | G | A | 1 | a0001c0001t0004g0237 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1024+3198G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744663 | |||||||
| chr7:744726 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1024+3261C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744726 | |||||||
| chr7:744746 | C | T | 1 | a0003c0003t0003g0150 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1024+3281C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744746 | |||||||
| chr7:744784 | A | G | 4 | a0001c0001t0003g0318 a0003c0012t0004g0056 a0011c0018t0010g0120 others(1): Show |
4 | HG01496.hp2 HG02280.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+3319A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744784 | |||||||
| chr7:744792 | A | G | 219 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1024+3327A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744792 | |||||||
| chr7:744794 | G | C | 6 | a0002c0002t0001g0025 a0002c0002t0001g0217 a0002c0002t0001g0224 others(3): Show |
7 | HG00738.hp2 HG01257.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024+3329G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744794 | |||||||
| chr7:744824 | A | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1024+3359A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744824 | |||||||
| chr7:744850 | G | A | 2 | a0002c0002t0009g0204 a0002c0002t0009g0295 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1024+3385G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744850 | |||||||
| chr7:744894 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1024+3429C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744894 | |||||||
| chr7:744950 | G | A | 4 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0003c0003t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+3485G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 744950 | |||||||
| chr7:745008 | C | T | 2 | a0003c0003t0003g0145 a0003c0003t0003g0150 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1024+3543C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745008 | |||||||
| chr7:745048 | G | C | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1024+3583G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745048 | |||||||
| chr7:745066 | C | T | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1024+3601C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745066 | |||||||
| chr7:745080 | T | A | 138 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(135): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1024+3615T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745080 | |||||||
| chr7:745081 | T | G | 138 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(135): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1024+3616T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745081 | |||||||
| chr7:745148 | C | T | 27 | a0003c0003t0003g0002 a0003c0003t0003g0020 a0003c0003t0003g0021 others(24): Show |
33 | HG01978.hp2 HG02027.hp1 HG02056.hp1 others(30): Show |
intron_variant | MODIFIER | c.1024+3683C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745148 | |||||||
| chr7:745194 | C | G | 1 | a0001c0004t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1024+3729C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745194 | |||||||
| chr7:745227 | C | T | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1024+3762C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745227 | |||||||
| chr7:745295 | C | T | 29 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1024+3830C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745295 | |||||||
| chr7:745306 | C | G | 65 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(62): Show |
79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1024+3841C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745306 | |||||||
| chr7:745340 | G | A | 1 | a0002c0002t0001g0317 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1024+3875G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745340 | |||||||
| chr7:745348 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1024+3883G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745348 | |||||||
| chr7:745373 | A | G | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1024+3908A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745373 | |||||||
| chr7:745402 | G | A | 1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1024+3937G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745402 | |||||||
| chr7:745417 | C | T | 3 | a0001c0001t0002g0331 a0001c0001t0002g0332 a0001c0001t0002g0333 |
3 | HG00544.hp1 HG00621.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1024+3952C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745417 | |||||||
| chr7:745427 | TAC | T | 3 | a0002c0002t0001g0293 a0002c0017t0001g0302 a0002c0025t0001g0312 |
3 | HG03130.hp2 HG03834.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1024+3976_1024+397 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 745427 | ||||||
| chr7:745429 | C | CACAA | 110 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(107): Show |
126 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1024+3967_1024+396 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 745429 | ||||||
| chr7:745433 | C | A | 24 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(21): Show |
26 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(23): Show |
intron_variant | MODIFIER | c.1024+3968C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745433 | |||||||
| chr7:745433 | C | G | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1024+3968C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745433 | |||||||
| chr7:745437 | C | T | 110 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(107): Show |
126 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1024+3972C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745437 | |||||||
| chr7:745463 | TAC | T | 11 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0034 others(8): Show |
13 | HG00741.hp2 HG01074.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1024+4007_1024+400 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 745463 | ||||||
| chr7:745473 | C | G | 1 | a0002c0002t0001g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1024+4008C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745473 | |||||||
| chr7:745493 | C | T | 3 | a0003c0012t0004g0056 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG01496.hp2 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1024+4028C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745493 | |||||||
| chr7:745507 | G | A | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1024+4042G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745507 | |||||||
| chr7:745522 | C | T | 1 | a0002c0002t0001g0283 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1024+4057C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745522 | |||||||
| chr7:745547 | G | A | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1024+4082G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745547 | |||||||
| chr7:745562 | C | T | 4 | a0002c0002t0001g0236 a0002c0002t0001g0252 a0002c0002t0001g0253 others(1): Show |
4 | HG00735.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+4097C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745562 | |||||||
| chr7:745567 | A | C | 1 | a0006c0011t0001g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1024+4102A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745567 | |||||||
| chr7:745619 | A | G | 1 | a0002c0002t0016g0251 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1024+4154A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745619 | |||||||
| chr7:745656 | CTT | C | 3 | a0002c0002t0001g0235 a0003c0003t0003g0151 a0003c0003t0005g0334 |
3 | HG01978.hp2 HG02155.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1024+4192_1024+419 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745656 | |||||||
| chr7:745666 | C | T | 1 | a0001c0001t0002g0330 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1024+4201C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745666 | |||||||
| chr7:745681 | A | G | 246 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(243): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1024+4216A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745681 | |||||||
| chr7:745688 | CAT | C | 60 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1024+4224_1024+422 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745688 | |||||||
| chr7:745703 | G | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1024+4238G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745703 | |||||||
| chr7:745719 | C | T | 3 | a0002c0002t0001g0202 a0002c0002t0001g0238 a0003c0003t0005g0334 |
3 | HG01433.hp1 HG01517.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1024+4254C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745719 | |||||||
| chr7:745723 | C | T | 5 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0016g0251 others(2): Show |
7 | HG01192.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024+4258C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745723 | |||||||
| chr7:745757 | C | T | 2 | a0002c0002t0001g0203 a0002c0002t0001g0282 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1024+4292C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745757 | |||||||
| chr7:745774 | C | T | 8 | a0003c0003t0003g0008 a0003c0003t0003g0126 a0003c0003t0003g0135 others(5): Show |
10 | HG00558.hp1 HG02040.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.1024+4309C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 745774 | |||||||
| chr7:746278 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1024+4813C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746278 | |||||||
| chr7:746279 | CT | C | 6 | a0001c0001t0002g0321 a0001c0001t0004g0170 a0001c0004t0001g0115 others(3): Show |
6 | HG01106.hp1 HG01109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024+4815delT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746279 | |||||||
| chr7:746280 | T | C | 150 | a0001c0001t0002g0068 a0001c0001t0002g0090 a0001c0001t0002g0092 others(147): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1024+4815T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746280 | |||||||
| chr7:746284 | C | T | 75 | a0001c0001t0002g0013 a0001c0001t0002g0063 a0001c0001t0002g0075 others(72): Show |
90 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.1024+4819C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746284 | |||||||
| chr7:746296 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1024+4831G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746296 | |||||||
| chr7:746313 | T | TCCCCCGC others(97): Show |
2 | a0001c0004t0001g0054 a0002c0002t0001g0316 |
2 | HG00099.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1024+4865_1024+486 others(108): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746313 | ||||||
| chr7:746313 | T | TCCCCCGC others(201): Show |
1 | a0001c0004t0001g0051 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1024+4865_1024+486 others(212): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746313 | ||||||
| chr7:746313 | T | TCCCCCGC others(201): Show |
1 | a0007c0013t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1024+4865_1024+486 others(212): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746313 | ||||||
| chr7:746315 | C | T | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1024+4850C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746315 | |||||||
| chr7:746324 | T | TCATGCCT others(149): Show |
1 | a0001c0001t0002g0086 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1024+4865_1024+486 others(160): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746324 | ||||||
| chr7:746324 | T | TCATGCCT others(201): Show |
1 | a0001c0001t0002g0085 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1024+4865_1024+486 others(212): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746324 | ||||||
| chr7:746324 | T | TCATGCCT others(305): Show |
1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1024+4865_1024+486 others(316): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746324 | ||||||
| chr7:746324 | TCATGCCC others(45): Show |
T | 120 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(117): Show |
139 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1024+4975_1024+502 others(56): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746324 | ||||||
| chr7:746324 | TCATGCCC others(97): Show |
T | 8 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0306 others(5): Show |
10 | HG01884.hp1 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1024+4923_1024+502 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746324 | ||||||
| chr7:746331 | C | T | 138 | a0001c0001t0002g0006 a0001c0001t0002g0189 a0001c0001t0006g0065 others(135): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1024+4866C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746331 | |||||||
| chr7:746383 | C | CAGGGCCT others(45): Show |
5 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(2): Show |
5 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024+4957_1024+495 others(56): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746383 | ||||||
| chr7:746383 | C | T | 93 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(90): Show |
109 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1024+4918C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746383 | |||||||
| chr7:746389 | CTGTGACG others(97): Show |
C | 15 | a0003c0003t0005g0256 a0003c0005t0005g0209 a0003c0005t0005g0210 others(12): Show |
15 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024+4950_1024+505 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746389 | ||||||
| chr7:746395 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1024+4930C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746395 | |||||||
| chr7:746397 | CCCTCCTT others(44): Show |
C | 1 | a0003c0003t0003g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1024+4935_1024+498 others(55): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746397 | ||||||
| chr7:746423 | A | G | 113 | a0001c0001t0002g0189 a0001c0001t0006g0065 a0001c0001t0014g0250 others(110): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1024+4958A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746423 | |||||||
| chr7:746427 | A | G | 116 | a0001c0001t0002g0189 a0001c0001t0014g0250 a0002c0002t0001g0009 others(113): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1024+4962A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746427 | |||||||
| chr7:746428 | A | ACATGCCT others(149): Show |
1 | a0002c0002t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1024+4969_1024+497 others(160): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746428 | ||||||
| chr7:746428 | A | T | 116 | a0001c0001t0002g0189 a0001c0001t0014g0250 a0002c0002t0001g0009 others(113): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1024+4963A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746428 | |||||||
| chr7:746435 | C | T | 123 | a0001c0001t0002g0005 a0001c0001t0002g0189 a0001c0001t0002g0306 others(120): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1024+4970C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746435 | |||||||
| chr7:746440 | C | T | 2 | a0001c0001t0003g0318 a0001c0001t0006g0095 |
2 | NA18522.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1024+4975C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746440 | |||||||
| chr7:746441 | C | CTGTGACG others(45): Show |
1 | a0003c0003t0007g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1024+5002_1024+505 others(56): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746441 | ||||||
| chr7:746441 | C | T | 2 | a0001c0001t0003g0318 a0001c0001t0006g0095 |
2 | NA18522.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1024+4976C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746441 | |||||||
| chr7:746441 | CTGTGACG others(45): Show |
C | 4 | a0002c0002t0001g0222 a0002c0002t0001g0223 a0002c0002t0001g0264 others(1): Show |
4 | HG00323.hp1 HG00642.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+5002_1024+505 others(56): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746441 | ||||||
| chr7:746469 | C | A | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1024+5004C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746469 | |||||||
| chr7:746484 | G | T | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1024+5019G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746484 | |||||||
| chr7:746487 | C | A | 2 | a0001c0001t0002g0092 a0001c0016t0012g0105 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1024+5022C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746487 | |||||||
| chr7:746511 | C | T | 2 | a0003c0003t0001g0111 a0003c0003t0001g0335 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1024+5046C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746511 | |||||||
| chr7:746557 | C | T | 11 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0325 others(8): Show |
12 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1024+5092C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746557 | |||||||
| chr7:746589 | G | A | 1 | a0003c0003t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1024+5124G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746589 | |||||||
| chr7:746593 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1024+5128G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746593 | |||||||
| chr7:746671 | T | A | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+5206T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746671 | |||||||
| chr7:746727 | G | A | 1 | a0003c0005t0005g0287 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1024+5262G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746727 | |||||||
| chr7:746815 | C | T | 1 | a0002c0002t0001g0200 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1024+5350C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746815 | |||||||
| chr7:746824 | C | T | 1 | a0001c0001t0014g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1024+5359C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746824 | |||||||
| chr7:746850 | T | C | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1024+5385T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746850 | |||||||
| chr7:746859 | C | T | 1 | a0002c0002t0001g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1024+5394C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 746859 | |||||||
| chr7:746980 | CCTT | C | 3 | a0001c0001t0004g0024 a0001c0001t0004g0107 a0001c0001t0004g0171 |
4 | NA18979.hp1 NA19005.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+5520_1024+552 others(7): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 746980 | ||||||
| chr7:747000 | T | A | 2 | a0001c0024t0011g0041 a0003c0012t0004g0056 |
2 | HG01496.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1024+5535T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747000 | |||||||
| chr7:747000 | T | G | 109 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1024+5535T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747000 | |||||||
| chr7:747046 | G | T | 2 | a0001c0001t0002g0326 a0001c0001t0002g0329 |
2 | NA19011.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1024+5581G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747046 | |||||||
| chr7:747099 | G | T | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(10): Show |
14 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1024+5634G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747099 | |||||||
| chr7:747142 | G | T | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1024+5677G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747142 | |||||||
| chr7:747195 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1024+5730C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747195 | |||||||
| chr7:747196 | A | G | 263 | a0001c0001t0002g0092 a0001c0001t0003g0318 a0001c0001t0004g0023 others(260): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1024+5731A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747196 | |||||||
| chr7:747217 | G | A | 1 | a0003c0003t0008g0100 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1024+5752G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747217 | |||||||
| chr7:747225 | G | A | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1024+5760G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747225 | |||||||
| chr7:747234 | C | T | 2 | a0001c0001t0002g0319 a0001c0004t0001g0039 |
2 | HG01255.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1024+5769C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747234 | |||||||
| chr7:747276 | G | C | 10 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0034 others(7): Show |
12 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+5811G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747276 | |||||||
| chr7:747397 | G | A | 3 | a0002c0002t0001g0222 a0002c0002t0001g0223 a0002c0002t0001g0264 |
3 | HG00323.hp1 HG00642.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1024+5932G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747397 | |||||||
| chr7:747402 | A | G | 1 | a0003c0005t0005g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1024+5937A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747402 | |||||||
| chr7:747420 | G | C | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1024+5955G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747420 | |||||||
| chr7:747482 | G | C | 4 | a0001c0001t0002g0092 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+6017G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747482 | |||||||
| chr7:747557 | T | C | 258 | a0001c0001t0002g0092 a0001c0001t0003g0318 a0001c0001t0004g0023 others(255): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1024+6092T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747557 | |||||||
| chr7:747564 | A | G | 262 | a0001c0001t0002g0092 a0001c0001t0003g0318 a0001c0001t0004g0023 others(259): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1024+6099A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747564 | |||||||
| chr7:747608 | T | G | 4 | a0003c0003t0003g0020 a0003c0003t0003g0137 a0003c0003t0003g0138 others(1): Show |
5 | HG03017.hp1 HG03490.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024+6143T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747608 | |||||||
| chr7:747612 | T | C | 4 | a0003c0003t0003g0020 a0003c0003t0003g0137 a0003c0003t0003g0138 others(1): Show |
5 | HG03017.hp1 HG03490.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024+6147T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747612 | |||||||
| chr7:747671 | A | G | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1024+6206A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747671 | |||||||
| chr7:747673 | TGTGTCCG others(225): Show |
T | 219 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(216): Show |
241 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1024+6267_1024+649 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 747673 | ||||||
| chr7:747673 | TGTGTCCG others(399): Show |
T | 27 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(24): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1024+6267_1025-645 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 747673 | ||||||
| chr7:747674 | GTGTCCGG others(51): Show |
G | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+6267_1024+632 others(62): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 747674 | ||||||
| chr7:747699 | C | T | 7 | a0001c0001t0002g0028 a0001c0001t0002g0319 a0001c0001t0002g0320 others(4): Show |
8 | NA18612.hp2 NA18955.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1024+6234C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747699 | |||||||
| chr7:747708 | TTGGTGGG others(228): Show |
T | 1 | a0002c0002t0001g0283 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1024+6247_1024+648 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 747708 | ||||||
| chr7:747912 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1024+6447G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747912 | |||||||
| chr7:747914 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1024+6449C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747914 | |||||||
| chr7:747964 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1024+6499G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 747964 | |||||||
| chr7:748085 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1025-6504C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748085 | |||||||
| chr7:748129 | G | A | 1 | a0002c0002t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1025-6460G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748129 | |||||||
| chr7:748148 | GGTGTGCA others(167): Show |
G | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-6430_1025-625 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 748148 | ||||||
| chr7:748204 | TTGGTGTG others(51): Show |
T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1025-6339_1025-628 others(62): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 748204 | ||||||
| chr7:748322 | A | G | 222 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1025-6267A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748322 | |||||||
| chr7:748484 | G | A | 1 | a0002c0002t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1025-6105G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748484 | |||||||
| chr7:748572 | G | A | 2 | a0001c0001t0002g0333 a0003c0003t0001g0111 |
2 | HG02074.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1025-6017G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748572 | |||||||
| chr7:748591 | C | T | 1 | a0003c0005t0005g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1025-5998C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748591 | |||||||
| chr7:748615 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025-5974C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748615 | |||||||
| chr7:748647 | G | A | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1025-5942G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748647 | |||||||
| chr7:748653 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1025-5936G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748653 | |||||||
| chr7:748683 | T | A | 5 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0328 others(2): Show |
6 | HG02056.hp2 NA18747.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025-5906T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748683 | |||||||
| chr7:748700 | G | A | 1 | a0002c0002t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1025-5889G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748700 | |||||||
| chr7:748962 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1025-5627A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748962 | |||||||
| chr7:748996 | G | C | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-5593G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 748996 | |||||||
| chr7:749114 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1025-5475C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749114 | |||||||
| chr7:749195 | G | A | 2 | a0003c0005t0005g0228 a0003c0005t0005g0259 |
2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1025-5394G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749195 | |||||||
| chr7:749271 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-5318C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749271 | |||||||
| chr7:749286 | T | G | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1025-5303T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749286 | |||||||
| chr7:749624 | C | T | 2 | a0002c0002t0001g0292 a0002c0002t0001g0293 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1025-4965C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749624 | |||||||
| chr7:749796 | G | A | 254 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(251): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1025-4793G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749796 | |||||||
| chr7:749809 | C | T | 2 | a0001c0001t0004g0170 a0001c0001t0004g0175 |
2 | HG02132.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1025-4780C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749809 | |||||||
| chr7:749823 | C | G | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1025-4766C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749823 | |||||||
| chr7:749912 | T | C | 1 | a0001c0001t0004g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1025-4677T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749912 | |||||||
| chr7:749987 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1025-4602C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 749987 | |||||||
| chr7:750220 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025-4369G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750220 | |||||||
| chr7:750263 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1025-4326C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750263 | |||||||
| chr7:750285 | G | T | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1025-4304G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750285 | |||||||
| chr7:750290 | G | A | 2 | a0002c0002t0001g0222 a0002c0002t0001g0223 |
2 | HG00642.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1025-4299G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750290 | |||||||
| chr7:750321 | C | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0189 |
3 | HG03491.hp2 HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1025-4268C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750321 | |||||||
| chr7:750330 | G | A | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1025-4259G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750330 | |||||||
| chr7:750369 | C | T | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025-4220C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750369 | |||||||
| chr7:750389 | C | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4200C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750389 | |||||||
| chr7:750390 | T | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4199T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750390 | |||||||
| chr7:750391 | T | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4198T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750391 | |||||||
| chr7:750395 | T | G | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4194T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750395 | |||||||
| chr7:750396 | G | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4193G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750396 | |||||||
| chr7:750398 | A | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4191A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750398 | |||||||
| chr7:750402 | G | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4187G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750402 | |||||||
| chr7:750405 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4184G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750405 | |||||||
| chr7:750408 | C | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4181C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750408 | |||||||
| chr7:750412 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4177G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750412 | |||||||
| chr7:750432 | T | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4157T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750432 | |||||||
| chr7:750433 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4156G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750433 | |||||||
| chr7:750435 | T | G | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4154T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750435 | |||||||
| chr7:750449 | A | G | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1025-4140A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750449 | |||||||
| chr7:750463 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4126G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750463 | |||||||
| chr7:750476 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4113G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750476 | |||||||
| chr7:750534 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4055G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750534 | |||||||
| chr7:750537 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4052G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750537 | |||||||
| chr7:750541 | G | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4048G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750541 | |||||||
| chr7:750542 | T | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4047T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750542 | |||||||
| chr7:750544 | A | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4045A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750544 | |||||||
| chr7:750551 | T | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4038T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750551 | |||||||
| chr7:750577 | G | A | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(10): Show |
14 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1025-4012G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750577 | |||||||
| chr7:750587 | C | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-4002C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750587 | |||||||
| chr7:750595 | A | C | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-3994A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750595 | |||||||
| chr7:750597 | T | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-3992T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750597 | |||||||
| chr7:750637 | C | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-3952C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750637 | |||||||
| chr7:750643 | C | G | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-3946C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750643 | |||||||
| chr7:750672 | T | A | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1025-3917T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750672 | |||||||
| chr7:750679 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1025-3910C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750679 | |||||||
| chr7:750836 | G | A | 1 | a0001c0001t0014g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1025-3753G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750836 | |||||||
| chr7:750870 | C | T | 5 | a0002c0002t0001g0203 a0002c0002t0001g0279 a0002c0002t0001g0280 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-3719C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 750870 | |||||||
| chr7:751070 | G | A | 1 | a0002c0002t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1025-3519G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751070 | |||||||
| chr7:751111 | A | G | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-3478A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751111 | |||||||
| chr7:751155 | A | G | 79 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(76): Show |
93 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.1025-3434A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751155 | |||||||
| chr7:751160 | C | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025-3429C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751160 | |||||||
| chr7:751161 | G | T | 1 | a0002c0002t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1025-3428G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751161 | |||||||
| chr7:751211 | A | C | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1025-3378A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751211 | |||||||
| chr7:751354 | C | T | 1 | a0003c0005t0005g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1025-3235C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751354 | |||||||
| chr7:751454 | C | T | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1025-3135C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751454 | |||||||
| chr7:751570 | AT | A | 72 | a0001c0001t0002g0329 a0001c0001t0004g0024 a0001c0001t0004g0107 others(69): Show |
86 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1025-2998delT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 751570 | ||||||
| chr7:751570 | ATT | A | 160 | a0001c0001t0003g0318 a0001c0001t0004g0176 a0001c0004t0001g0004 others(157): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1025-2999_1025-299 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 751570 | ||||||
| chr7:751570 | ATTT | A | 9 | a0001c0004t0001g0040 a0001c0004t0001g0043 a0001c0004t0001g0044 others(6): Show |
9 | HG01074.hp1 HG01496.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025-3000_1025-299 others(7): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 751570 | ||||||
| chr7:751633 | G | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-2956G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751633 | |||||||
| chr7:751785 | G | C | 53 | a0001c0004t0001g0048 a0002c0002t0001g0009 a0002c0002t0001g0025 others(50): Show |
58 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1025-2804G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 751785 | |||||||
| chr7:751939 | CTGAT | C | 3 | a0005c0007t0001g0152 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1025-2647_1025-264 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 751939 | ||||||
| chr7:752023 | C | T | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025-2566C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752023 | |||||||
| chr7:752118 | G | A | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1025-2471G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752118 | |||||||
| chr7:752239 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1025-2350C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752239 | |||||||
| chr7:752283 | A | G | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1025-2306A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752283 | |||||||
| chr7:752300 | T | C | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2289T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752300 | |||||||
| chr7:752306 | A | C | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2283A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752306 | |||||||
| chr7:752307 | G | A | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2282G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752307 | |||||||
| chr7:752308 | T | C | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2281T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752308 | |||||||
| chr7:752327 | T | C | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2262T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752327 | |||||||
| chr7:752334 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1025-2255C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752334 | |||||||
| chr7:752349 | G | A | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2240G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752349 | |||||||
| chr7:752349 | G | GCAGAGTG others(273): Show |
1 | a0003c0003t0007g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025-2143_1025-214 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752349 | ||||||
| chr7:752354 | G | A | 6 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0127 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-2235G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752354 | |||||||
| chr7:752354 | G | GTGATGAC others(273): Show |
1 | a0003c0003t0007g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1025-2213_1025-221 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(133): Show |
6 | a0002c0002t0001g0294 a0002c0002t0001g0297 a0002c0002t0001g0298 others(3): Show |
6 | HG01167.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025-2096_1025-209 others(144): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(273): Show |
1 | a0002c0002t0001g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1025-2143_1025-214 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(273): Show |
182 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(179): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1025-2143_1025-214 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(413): Show |
3 | a0001c0001t0004g0169 a0003c0003t0003g0190 a0003c0003t0003g0191 |
3 | HG00621.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1025-2143_1025-214 others(424): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(553): Show |
1 | a0005c0007t0003g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1025-2143_1025-214 others(564): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(273): Show |
1 | a0003c0003t0007g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1025-2143_1025-214 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(274): Show |
1 | a0003c0003t0003g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1025-2143_1025-214 others(285): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752354 | G | GTGATGAC others(273): Show |
17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025-2150_1025-214 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752354 | ||||||
| chr7:752377 | G | GCGGGCCG others(273): Show |
2 | a0003c0003t0001g0111 a0005c0007t0001g0152 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1025-2143_1025-214 others(284): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752377 | ||||||
| chr7:752379 | G | GGGCCGGG others(133): Show |
1 | a0002c0002t0001g0296 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1025-2096_1025-209 others(144): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752379 | ||||||
| chr7:752391 | G | GCTTCCCT others(133): Show |
38 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(35): Show |
40 | HG01496.hp2 HG01884.hp1 HG02132.hp1 others(37): Show |
intron_variant | MODIFIER | c.1025-2143_1025-214 others(144): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 752391 | ||||||
| chr7:752423 | A | G | 1 | a0003c0003t0003g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1025-2166A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752423 | |||||||
| chr7:752494 | G | A | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1025-2095G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752494 | |||||||
| chr7:752518 | C | T | 1 | a0002c0002t0015g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1025-2071C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752518 | |||||||
| chr7:752587 | G | A | 1 | a0005c0007t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1025-2002G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752587 | |||||||
| chr7:752658 | T | C | 262 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(259): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1025-1931T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752658 | |||||||
| chr7:752691 | A | G | 1 | a0003c0005t0005g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1025-1898A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752691 | |||||||
| chr7:752720 | A | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025-1869A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752720 | |||||||
| chr7:752722 | G | T | 1 | a0002c0002t0009g0299 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1025-1867G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752722 | |||||||
| chr7:752763 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1025-1826G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752763 | |||||||
| chr7:752787 | A | G | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025-1802A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752787 | |||||||
| chr7:752841 | A | T | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1025-1748A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752841 | |||||||
| chr7:752875 | A | G | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-1714A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752875 | |||||||
| chr7:752890 | T | C | 1 | a0003c0003t0003g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1025-1699T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752890 | |||||||
| chr7:752967 | G | A | 2 | a0003c0003t0003g0140 a0003c0003t0008g0180 |
2 | HG02698.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1025-1622G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752967 | |||||||
| chr7:752976 | C | T | 1 | a0002c0002t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1025-1613C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752976 | |||||||
| chr7:752989 | A | G | 2 | a0002c0002t0001g0195 a0002c0002t0013g0199 |
2 | HG00609.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1025-1600A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 752989 | |||||||
| chr7:753025 | G | A | 2 | a0001c0001t0002g0092 a0002c0002t0001g0281 |
2 | HG01943.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1025-1564G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753025 | |||||||
| chr7:753031 | C | CT | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-1555dupT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753031 | ||||||
| chr7:753044 | A | C | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-1545A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753044 | |||||||
| chr7:753336 | T | C | 262 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(259): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1025-1253T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753336 | |||||||
| chr7:753440 | C | T | 1 | a0002c0002t0001g0205 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1025-1149C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753440 | |||||||
| chr7:753542 | T | C | 1 | a0002c0002t0001g0266 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1025-1047T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753542 | |||||||
| chr7:753557 | G | A | 1 | a0002c0002t0001g0267 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1025-1032G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753557 | |||||||
| chr7:753601 | G | GTC | 230 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1025-983_1025-982d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753601 | ||||||
| chr7:753621 | G | A | 1 | a0003c0003t0007g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1025-968G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753621 | |||||||
| chr7:753635 | A | G | 276 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1025-954A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753635 | |||||||
| chr7:753662 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1025-927C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753662 | |||||||
| chr7:753715 | CAT | C | 3 | a0002c0002t0001g0018 a0002c0002t0001g0201 a0002c0002t0001g0215 |
4 | HG02886.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-871_1025-870d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753715 | ||||||
| chr7:753731 | C | T | 1 | a0017c0029t0010g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1025-858C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753731 | |||||||
| chr7:753742 | C | T | 5 | a0001c0004t0001g0042 a0001c0004t0001g0045 a0001c0004t0001g0046 others(2): Show |
5 | HG00140.hp2 HG01192.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-847C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753742 | |||||||
| chr7:753748 | GATC | G | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025-838_1025-836d others(5): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753748 | ||||||
| chr7:753776 | GTCTCTCT others(101): Show |
G | 1 | a0002c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1025-775_1025-668d others(2): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753776 | ||||||
| chr7:753780 | CTCTCA | C | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1025-806_1025-802d others(7): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753780 | ||||||
| chr7:753795 | G | A | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1025-794G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753795 | |||||||
| chr7:753810 | G | T | 78 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(75): Show |
92 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1025-779G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753810 | |||||||
| chr7:753812 | GTCTC | G | 4 | a0001c0001t0004g0108 a0002c0002t0001g0009 a0002c0002t0001g0182 others(1): Show |
6 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-772_1025-769d others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753812 | ||||||
| chr7:753848 | GTC | G | 5 | a0002c0002t0001g0203 a0002c0002t0001g0279 a0002c0002t0001g0280 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-735_1025-734d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753848 | ||||||
| chr7:753869 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-720C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753869 | |||||||
| chr7:753882 | GTC | G | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1025-698_1025-697d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753882 | ||||||
| chr7:753890 | CTCA | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025-694_1025-692d others(5): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753890 | ||||||
| chr7:753917 | C | T | 1 | a0003c0003t0003g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1025-672C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753917 | |||||||
| chr7:753958 | G | GTCTCTCT others(101): Show |
1 | a0001c0004t0001g0042 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1025-594_1025-593i others(110): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753958 | ||||||
| chr7:753960 | C | CTCTCATC others(63): Show |
1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1025-625_1025-624i others(72): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753960 | ||||||
| chr7:753964 | CTCA | C | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-620_1025-618d others(5): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | 753964 | ||||||
| chr7:753976 | C | T | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025-613C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753976 | |||||||
| chr7:753983 | T | C | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1025-606T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753983 | |||||||
| chr7:753992 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025-597G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 753992 | |||||||
| chr7:754030 | G | A | 1 | a0005c0007t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1025-559G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754030 | |||||||
| chr7:754049 | G | A | 1 | a0006c0011t0001g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1025-540G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754049 | |||||||
| chr7:754076 | G | T | 7 | a0002c0002t0001g0294 a0002c0002t0001g0296 a0002c0002t0001g0297 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025-513G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754076 | |||||||
| chr7:754130 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025-459G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754130 | |||||||
| chr7:754168 | A | C | 1 | a0003c0003t0003g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1025-421A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754168 | |||||||
| chr7:754255 | G | A | 1 | a0002c0002t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1025-334G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754255 | |||||||
| chr7:754290 | A | C | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1025-299A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754290 | |||||||
| chr7:754317 | G | A | 78 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(75): Show |
92 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1025-272G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754317 | |||||||
| chr7:754335 | A | G | 2 | a0003c0003t0003g0145 a0003c0003t0003g0150 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1025-254A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754335 | |||||||
| chr7:754455 | C | T | 60 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1025-134C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754455 | |||||||
| chr7:754458 | C | T | 1 | a0002c0002t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1025-131C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754458 | |||||||
| chr7:754551 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1025-38T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754551 | |||||||
| chr7:754560 | C | T | 1 | a0016c0028t0004g0173 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1025-29C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 4/12 | chr7 | 754560 | |||||||
| chr7:754834 | A | G | 260 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(257): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1257+13A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 754834 | |||||||
| chr7:754851 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1257+30G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 754851 | |||||||
| chr7:754939 | C | T | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1257+118C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 754939 | |||||||
| chr7:754991 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0085 a0001c0001t0002g0086 |
4 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+170C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 754991 | |||||||
| chr7:755176 | A | G | 276 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1257+355A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755176 | |||||||
| chr7:755219 | C | A | 1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1257+398C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755219 | |||||||
| chr7:755227 | C | T | 1 | a0003c0003t0003g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1257+406C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755227 | |||||||
| chr7:755248 | C | T | 2 | a0002c0002t0015g0303 a0003c0003t0008g0155 |
2 | NA18959.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1257+427C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755248 | |||||||
| chr7:755279 | G | T | 1 | a0002c0002t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1257+458G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755279 | |||||||
| chr7:755326 | C | T | 29 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1257+505C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755326 | |||||||
| chr7:755327 | G | A | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1257+506G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755327 | |||||||
| chr7:755590 | A | G | 228 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(225): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1257+769A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755590 | |||||||
| chr7:755618 | G | A | 2 | a0003c0003t0003g0059 a0003c0003t0003g0153 |
2 | NA18948.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1257+797G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755618 | |||||||
| chr7:755648 | T | G | 1 | a0002c0002t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1257+827T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755648 | |||||||
| chr7:755658 | G | A | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1257+837G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755658 | |||||||
| chr7:755669 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1257+848C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755669 | |||||||
| chr7:755704 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1257+883C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755704 | |||||||
| chr7:755723 | G | A | 323 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(320): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1257+902G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755723 | |||||||
| chr7:755801 | A | G | 1 | a0003c0003t0003g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1257+980A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755801 | |||||||
| chr7:755866 | C | A | 1 | a0002c0002t0001g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1258-916C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755866 | |||||||
| chr7:755887 | G | A | 1 | a0003c0003t0003g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1258-895G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 755887 | |||||||
| chr7:756001 | G | GGT | 262 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(259): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1258-773_1258-772d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 756001 | ||||||
| chr7:756049 | A | G | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1258-733A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756049 | |||||||
| chr7:756074 | CGGTGCAG others(38): Show |
C | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1258-677_1258-633d others(47): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 756074 | ||||||
| chr7:756105 | A | G | 226 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1258-677A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756105 | |||||||
| chr7:756119 | T | C | 4 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(1): Show |
4 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-663T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756119 | |||||||
| chr7:756120 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1258-662G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756120 | |||||||
| chr7:756150 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1258-632G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756150 | |||||||
| chr7:756164 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1258-618C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756164 | |||||||
| chr7:756165 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0099 |
3 | HG01175.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1258-617G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756165 | |||||||
| chr7:756194 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1258-588C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756194 | |||||||
| chr7:756211 | G | A | 3 | a0003c0003t0003g0190 a0003c0003t0003g0191 a0005c0007t0003g0142 |
3 | HG02630.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1258-571G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756211 | |||||||
| chr7:756227 | G | A | 1 | a0001c0001t0004g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1258-555G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756227 | |||||||
| chr7:756577 | C | T | 1 | a0002c0002t0001g0268 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1258-205C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756577 | |||||||
| chr7:756593 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1258-189G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756593 | |||||||
| chr7:756622 | C | T | 29 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1258-160C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756622 | |||||||
| chr7:756716 | G | A | 27 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(24): Show |
29 | HG00621.hp1 HG02132.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.1258-66G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 5/12 | chr7 | 756716 | |||||||
| chr7:757021 | T | G | 1 | a0003c0003t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1470+27T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757021 | |||||||
| chr7:757057 | A | G | 2 | a0002c0002t0001g0294 a0002c0002t0001g0298 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1470+63A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757057 | |||||||
| chr7:757122 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1470+128C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757122 | |||||||
| chr7:757162 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1470+168C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757162 | |||||||
| chr7:757242 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1470+248G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757242 | |||||||
| chr7:757246 | C | T | 228 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(225): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1470+252C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757246 | |||||||
| chr7:757250 | C | T | 1 | a0001c0001t0006g0104 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1470+256C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757250 | |||||||
| chr7:757268 | C | T | 20 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(17): Show |
20 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1470+274C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757268 | |||||||
| chr7:757278 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1470+284C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757278 | |||||||
| chr7:757313 | C | CTG | 231 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(228): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1470+319_1470+320i others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757313 | |||||||
| chr7:757388 | A | G | 1 | a0001c0004t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1470+394A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757388 | |||||||
| chr7:757495 | C | T | 106 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(103): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1470+501C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757495 | |||||||
| chr7:757682 | G | A | 31 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(28): Show |
33 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1470+688G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757682 | |||||||
| chr7:757788 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1470+794G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757788 | |||||||
| chr7:757791 | C | T | 1 | a0001c0004t0001g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1470+797C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757791 | |||||||
| chr7:757868 | C | A | 109 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1470+874C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757868 | |||||||
| chr7:757869 | C | T | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1470+875C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757869 | |||||||
| chr7:757916 | C | T | 1 | a0002c0008t0001g0277 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1470+922C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757916 | |||||||
| chr7:757948 | C | T | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1470+954C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 757948 | |||||||
| chr7:758041 | C | T | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1470+1047C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758041 | |||||||
| chr7:758078 | G | A | 226 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1470+1084G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758078 | |||||||
| chr7:758210 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1470+1216G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758210 | |||||||
| chr7:758442 | G | A | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1470+1448G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758442 | |||||||
| chr7:758611 | C | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1470+1617C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758611 | |||||||
| chr7:758786 | G | A | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1470+1792G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758786 | |||||||
| chr7:758911 | G | A | 1 | a0001c0004t0001g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1470+1917G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758911 | |||||||
| chr7:758934 | C | T | 3 | a0003c0003t0004g0109 a0003c0003t0007g0231 a0003c0003t0007g0232 |
3 | HG01891.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1470+1940C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758934 | |||||||
| chr7:758972 | C | T | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1470+1978C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 758972 | |||||||
| chr7:759065 | TCTGTGCT others(12): Show |
T | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1470+2085_1470+210 others(23): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 759065 | ||||||
| chr7:759082 | C | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1470+2088C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 759082 | |||||||
| chr7:759082 | C | T | 1 | a0003c0003t0003g0019 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1470+2088C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 759082 | |||||||
| chr7:759224 | T | C | 1 | a0003c0003t0008g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1470+2230T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 759224 | |||||||
| chr7:759438 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1471-2315G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 759438 | |||||||
| chr7:759734 | C | T | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1471-2019C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 759734 | |||||||
| chr7:759839 | C | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1471-1914C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 759839 | |||||||
| chr7:760001 | C | A | 1 | a0003c0003t0003g0123 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1471-1752C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760001 | |||||||
| chr7:760056 | CGAGGGAG others(27): Show |
C | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1471-1663_1471-163 others(38): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 760056 | ||||||
| chr7:760073 | C | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1471-1680C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760073 | |||||||
| chr7:760090 | T | C | 4 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(1): Show |
4 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1471-1663T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760090 | |||||||
| chr7:760176 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1471-1577C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760176 | |||||||
| chr7:760243 | G | A | 1 | a0001c0001t0004g0185 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1471-1510G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760243 | |||||||
| chr7:760510 | C | T | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1471-1243C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760510 | |||||||
| chr7:760532 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1471-1221C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760532 | |||||||
| chr7:760553 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1471-1200G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760553 | |||||||
| chr7:760556 | A | G | 1 | a0002c0002t0001g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1471-1197A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760556 | |||||||
| chr7:760668 | T | G | 12 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0325 others(9): Show |
13 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1471-1085T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 760668 | |||||||
| chr7:761067 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1471-686C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761067 | |||||||
| chr7:761203 | C | G | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1471-550C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761203 | |||||||
| chr7:761209 | C | T | 1 | a0001c0001t0006g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1471-544C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761209 | |||||||
| chr7:761252 | T | TG | 150 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(147): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1471-496dupG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 761252 | ||||||
| chr7:761302 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1471-451C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761302 | |||||||
| chr7:761319 | G | A | 2 | a0002c0002t0001g0218 a0002c0026t0001g0211 |
2 | HG01978.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1471-434G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761319 | |||||||
| chr7:761340 | A | G | 262 | a0001c0001t0002g0092 a0001c0001t0003g0318 a0001c0001t0004g0023 others(259): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1471-413A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761340 | |||||||
| chr7:761360 | G | C | 30 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(27): Show |
32 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(29): Show |
intron_variant | MODIFIER | c.1471-393G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761360 | |||||||
| chr7:761412 | G | A | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1471-341G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761412 | |||||||
| chr7:761510 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1471-243G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761510 | |||||||
| chr7:761574 | C | T | 200 | a0001c0001t0003g0318 a0002c0002t0001g0009 a0002c0002t0001g0011 others(197): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1471-179C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 6/12 | chr7 | 761574 | |||||||
| chr7:761997 | T | TTGAGCCC others(17): Show |
259 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(256): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1614+104_1614+105i others(26): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 761997 | ||||||
| chr7:762030 | C | G | 2 | a0003c0005t0005g0228 a0003c0005t0005g0259 |
2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1614+134C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762030 | |||||||
| chr7:762155 | C | G | 226 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1614+259C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762155 | |||||||
| chr7:762170 | T | A | 1 | a0002c0002t0001g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1614+274T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762170 | |||||||
| chr7:762218 | T | G | 230 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1614+322T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762218 | |||||||
| chr7:762223 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1614+327C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762223 | |||||||
| chr7:762317 | C | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1614+421C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762317 | |||||||
| chr7:762442 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1614+546G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762442 | |||||||
| chr7:762487 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1614+591G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762487 | |||||||
| chr7:762490 | C | CA | 32 | a0001c0001t0002g0058 a0001c0001t0002g0063 a0001c0001t0002g0189 others(29): Show |
34 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1614+608dupA | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 762490 | ||||||
| chr7:762490 | CA | C | 18 | a0001c0001t0002g0082 a0003c0003t0005g0256 a0003c0003t0005g0334 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1614+608delA | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 762490 | ||||||
| chr7:762505 | G | A | 14 | a0002c0002t0001g0026 a0002c0002t0001g0195 a0002c0002t0001g0196 others(11): Show |
15 | HG00609.hp1 HG00609.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1614+609G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762505 | |||||||
| chr7:762537 | G | C | 1 | a0003c0003t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1614+641G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762537 | |||||||
| chr7:762571 | C | T | 2 | a0003c0003t0003g0132 a0003c0003t0003g0133 |
2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1614+675C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762571 | |||||||
| chr7:762669 | A | G | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1614+773A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762669 | |||||||
| chr7:762845 | T | G | 1 | a0002c0002t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1614+949T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762845 | |||||||
| chr7:762921 | C | G | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1615-885C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762921 | |||||||
| chr7:762942 | C | A | 2 | a0002c0017t0001g0302 a0002c0025t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-864C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 762942 | |||||||
| chr7:763058 | C | A | 1 | a0003c0005t0005g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1615-748C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763058 | |||||||
| chr7:763249 | C | G | 230 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1615-557C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763249 | |||||||
| chr7:763288 | G | A | 1 | a0017c0029t0010g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1615-518G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763288 | |||||||
| chr7:763291 | A | G | 259 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(256): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1615-515A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763291 | |||||||
| chr7:763317 | C | T | 59 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(56): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1615-489C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763317 | |||||||
| chr7:763450 | G | A | 1 | a0003c0003t0003g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1615-356G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763450 | |||||||
| chr7:763538 | T | C | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1615-268T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763538 | |||||||
| chr7:763607 | C | T | 60 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1615-199C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763607 | |||||||
| chr7:763679 | C | T | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1615-127C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763679 | |||||||
| chr7:763705 | G | A | 105 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(102): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1615-101G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 7/12 | chr7 | 763705 | |||||||
| chr7:764059 | C | T | 4 | a0001c0001t0002g0016 a0003c0003t0007g0101 a0003c0003t0007g0102 others(1): Show |
5 | HG00639.hp1 HG01099.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1783+85C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764059 | |||||||
| chr7:764130 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1783+156A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764130 | |||||||
| chr7:764153 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1783+179C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764153 | |||||||
| chr7:764264 | A | C | 1 | a0003c0003t0003g0143 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1783+290A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764264 | |||||||
| chr7:764318 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1783+344G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764318 | |||||||
| chr7:764431 | T | C | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783+457T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764431 | |||||||
| chr7:764438 | C | T | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1783+464C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764438 | |||||||
| chr7:764445 | A | G | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783+471A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764445 | |||||||
| chr7:764527 | C | T | 1 | a0002c0002t0015g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1783+553C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764527 | |||||||
| chr7:764538 | C | T | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1783+564C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764538 | |||||||
| chr7:764539 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783+565G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764539 | |||||||
| chr7:764552 | C | T | 1 | a0003c0003t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1783+578C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764552 | |||||||
| chr7:764582 | G | A | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1783+608G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764582 | |||||||
| chr7:764664 | G | A | 1 | a0003c0003t0003g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1783+690G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764664 | |||||||
| chr7:764797 | G | A | 59 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(56): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1783+823G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764797 | |||||||
| chr7:764855 | G | T | 1 | a0001c0001t0004g0166 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1783+881G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764855 | |||||||
| chr7:764889 | G | A | 1 | a0002c0002t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1783+915G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 764889 | |||||||
| chr7:764999 | T | TGGCC | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783+1026_1783+102 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 764999 | ||||||
| chr7:765053 | C | G | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1783+1079C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765053 | |||||||
| chr7:765148 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783+1174G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765148 | |||||||
| chr7:765302 | C | T | 4 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(1): Show |
4 | HG01192.hp2 HG02055.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783+1328C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765302 | |||||||
| chr7:765328 | C | G | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1783+1354C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765328 | |||||||
| chr7:765504 | C | T | 1 | a0001c0001t0014g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1783+1530C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765504 | |||||||
| chr7:765614 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1783+1640G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765614 | |||||||
| chr7:765693 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1783+1719G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765693 | |||||||
| chr7:765726 | G | C | 61 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(58): Show |
75 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1783+1752G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765726 | |||||||
| chr7:765786 | A | T | 1 | a0002c0002t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1783+1812A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765786 | |||||||
| chr7:765793 | C | T | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1783+1819C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765793 | |||||||
| chr7:765838 | T | C | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1783+1864T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765838 | |||||||
| chr7:765887 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1783+1913G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765887 | |||||||
| chr7:765931 | C | T | 2 | a0003c0005t0005g0287 a0003c0005t0005g0288 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1783+1957C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765931 | |||||||
| chr7:765980 | T | C | 260 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(257): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1783+2006T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765980 | |||||||
| chr7:765985 | C | T | 2 | a0001c0004t0001g0035 a0001c0004t0001g0036 |
2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1783+2011C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 765985 | |||||||
| chr7:766200 | T | C | 199 | a0001c0001t0003g0318 a0002c0002t0001g0009 a0002c0002t0001g0011 others(196): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1783+2226T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766200 | |||||||
| chr7:766240 | C | T | 3 | a0003c0003t0004g0109 a0003c0003t0007g0231 a0003c0003t0007g0232 |
3 | HG01891.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1783+2266C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766240 | |||||||
| chr7:766415 | G | A | 149 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(146): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1783+2441G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766415 | |||||||
| chr7:766503 | T | C | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1783+2529T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766503 | |||||||
| chr7:766791 | C | A | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1783+2817C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766791 | |||||||
| chr7:766833 | CCAAA | C | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1783+2866_1783+286 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 766833 | ||||||
| chr7:766936 | T | C | 2 | a0002c0002t0001g0270 a0002c0002t0001g0305 |
2 | NA18959.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1783+2962T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766936 | |||||||
| chr7:766966 | G | A | 1 | a0002c0002t0001g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1783+2992G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 766966 | |||||||
| chr7:767005 | C | G | 4 | a0002c0002t0001g0248 a0002c0002t0001g0262 a0002c0002t0001g0263 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783+3031C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767005 | |||||||
| chr7:767011 | A | G | 276 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1783+3037A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767011 | |||||||
| chr7:767022 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1783+3048G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767022 | |||||||
| chr7:767036 | G | A | 138 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(135): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1783+3062G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767036 | |||||||
| chr7:767067 | G | A | 2 | a0003c0003t0003g0131 a0003c0003t0003g0188 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1783+3093G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767067 | |||||||
| chr7:767074 | C | G | 1 | a0002c0002t0001g0201 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1783+3100C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767074 | |||||||
| chr7:767111 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783+3137C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767111 | |||||||
| chr7:767170 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1783+3196C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767170 | |||||||
| chr7:767217 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1783+3243C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767217 | |||||||
| chr7:767225 | C | T | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1784-3246C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767225 | |||||||
| chr7:767238 | C | CA | 41 | a0001c0001t0002g0068 a0001c0001t0002g0092 a0001c0001t0002g0103 others(38): Show |
43 | HG00099.hp2 HG00621.hp1 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.1784-3215dupA | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 767238 | ||||||
| chr7:767238 | C | CAA | 11 | a0001c0001t0004g0107 a0001c0001t0004g0177 a0001c0001t0004g0187 others(8): Show |
11 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1784-3216_1784-321 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 767238 | ||||||
| chr7:767257 | G | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1784-3214G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767257 | |||||||
| chr7:767261 | G | C | 1 | a0003c0005t0005g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1784-3210G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767261 | |||||||
| chr7:767299 | T | TAAAC | 231 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(228): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1784-3171_1784-317 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 767299 | ||||||
| chr7:767311 | A | C | 1 | a0002c0002t0001g0244 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1784-3160A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767311 | |||||||
| chr7:767352 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1784-3119C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767352 | |||||||
| chr7:767361 | C | G | 228 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(225): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1784-3110C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767361 | |||||||
| chr7:767378 | C | G | 61 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(58): Show |
75 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1784-3093C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767378 | |||||||
| chr7:767627 | A | G | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1784-2844A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767627 | |||||||
| chr7:767733 | C | A | 332 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(329): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1784-2738C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767733 | |||||||
| chr7:767743 | G | A | 109 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1784-2728G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767743 | |||||||
| chr7:767760 | G | A | 1 | a0015c0027t0003g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1784-2711G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767760 | |||||||
| chr7:767768 | G | C | 2 | a0002c0002t0001g0218 a0002c0026t0001g0211 |
2 | HG01978.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1784-2703G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767768 | |||||||
| chr7:767816 | C | G | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1784-2655C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767816 | |||||||
| chr7:767885 | G | C | 228 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(225): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1784-2586G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767885 | |||||||
| chr7:767928 | G | A | 1 | a0002c0008t0001g0271 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1784-2543G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767928 | |||||||
| chr7:767951 | G | C | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1784-2520G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 767951 | |||||||
| chr7:768005 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1784-2466C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768005 | |||||||
| chr7:768012 | G | A | 226 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1784-2459G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768012 | |||||||
| chr7:768025 | G | T | 1 | a0006c0011t0001g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1784-2446G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768025 | |||||||
| chr7:768032 | C | G | 1 | a0003c0003t0003g0153 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1784-2439C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768032 | |||||||
| chr7:768060 | CGGGCGGA others(52): Show |
C | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1784-2396_1784-233 others(63): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 768060 | ||||||
| chr7:768074 | C | T | 78 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(75): Show |
92 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1784-2397C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768074 | |||||||
| chr7:768082 | G | C | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1784-2389G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768082 | |||||||
| chr7:768120 | GGGCGGAA others(49): Show |
G | 78 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(75): Show |
92 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1784-2330_1784-227 others(60): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 768120 | ||||||
| chr7:768144 | C | T | 149 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(146): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1784-2327C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768144 | |||||||
| chr7:768161 | G | A | 1 | a0013c0009t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1784-2310G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768161 | |||||||
| chr7:768255 | G | C | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1784-2216G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768255 | |||||||
| chr7:768265 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1784-2206T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768265 | |||||||
| chr7:768267 | G | T | 2 | a0002c0017t0001g0302 a0002c0025t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1784-2204G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768267 | |||||||
| chr7:768321 | A | G | 1 | a0003c0003t0003g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1784-2150A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768321 | |||||||
| chr7:768327 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1784-2144C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768327 | |||||||
| chr7:768352 | TGGCGGAA others(52): Show |
T | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1784-2099_1784-204 others(63): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 768352 | ||||||
| chr7:768365 | T | A | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1784-2106T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768365 | |||||||
| chr7:768365 | T | C | 219 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(216): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1784-2106T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768365 | |||||||
| chr7:768372 | T | C | 220 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(217): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1784-2099T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768372 | |||||||
| chr7:768382 | C | T | 2 | a0002c0002t0001g0026 a0002c0022t0001g0304 |
2 | HG02080.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1784-2089C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768382 | |||||||
| chr7:768387 | A | C | 25 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(22): Show |
27 | HG00621.hp1 HG02132.hp1 NA18612.hp1 others(24): Show |
intron_variant | MODIFIER | c.1784-2084A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768387 | |||||||
| chr7:768432 | G | T | 3 | a0003c0003t0004g0109 a0003c0003t0007g0231 a0003c0003t0007g0232 |
3 | HG01891.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1784-2039G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768432 | |||||||
| chr7:768435 | T | C | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2036T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768435 | |||||||
| chr7:768436 | G | A | 230 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1784-2035G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768436 | |||||||
| chr7:768436 | G | C | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2035G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768436 | |||||||
| chr7:768438 | G | C | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2033G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768438 | |||||||
| chr7:768439 | C | A | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2032C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768439 | |||||||
| chr7:768444 | C | A | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2027C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768444 | |||||||
| chr7:768445 | G | C | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2026G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768445 | |||||||
| chr7:768446 | G | A | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2025G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768446 | |||||||
| chr7:768456 | C | A | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1784-2015C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768456 | |||||||
| chr7:768481 | T | C | 1 | a0003c0003t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1784-1990T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768481 | |||||||
| chr7:768541 | C | T | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1784-1930C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768541 | |||||||
| chr7:768573 | G | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1784-1898G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768573 | |||||||
| chr7:768576 | A | G | 109 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1784-1895A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768576 | |||||||
| chr7:768604 | C | G | 1 | a0004c0006t0001g0309 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1784-1867C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768604 | |||||||
| chr7:768654 | G | C | 1 | a0002c0002t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1784-1817G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768654 | |||||||
| chr7:768667 | C | T | 202 | a0001c0001t0003g0318 a0002c0002t0001g0009 a0002c0002t0001g0011 others(199): Show |
224 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1784-1804C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768667 | |||||||
| chr7:768671 | C | T | 5 | a0002c0002t0001g0203 a0002c0002t0001g0279 a0002c0002t0001g0280 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1784-1800C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768671 | |||||||
| chr7:768701 | C | G | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1784-1770C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768701 | |||||||
| chr7:768768 | T | G | 235 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0081 others(232): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1784-1703T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768768 | |||||||
| chr7:768796 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1784-1675G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768796 | |||||||
| chr7:768851 | G | T | 1 | a0001c0001t0004g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1784-1620G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768851 | |||||||
| chr7:768878 | G | T | 2 | a0002c0002t0001g0011 a0010c0020t0001g0011 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1784-1593G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768878 | |||||||
| chr7:768951 | C | T | 106 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(103): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1784-1520C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 768951 | |||||||
| chr7:769052 | A | G | 1 | a0002c0002t0001g0227 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1784-1419A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769052 | |||||||
| chr7:769112 | C | T | 48 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(45): Show |
51 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1784-1359C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769112 | |||||||
| chr7:769173 | C | G | 106 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(103): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1784-1298C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769173 | |||||||
| chr7:769249 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1784-1222C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769249 | |||||||
| chr7:769317 | C | T | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1784-1154C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769317 | |||||||
| chr7:769489 | A | G | 1 | a0001c0004t0001g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1784-982A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769489 | |||||||
| chr7:769491 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1784-980C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769491 | |||||||
| chr7:769644 | T | G | 227 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(224): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1784-827T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769644 | |||||||
| chr7:769714 | A | G | 1 | a0002c0002t0001g0027 | 2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1784-757A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769714 | |||||||
| chr7:769820 | G | C | 4 | a0001c0001t0006g0065 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02015.hp2 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784-651G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769820 | |||||||
| chr7:769879 | G | A | 1 | a0001c0001t0002g0321 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1784-592G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769879 | |||||||
| chr7:769922 | T | C | 1 | a0003c0005t0005g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1784-549T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 769922 | |||||||
| chr7:770107 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1784-364A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770107 | |||||||
| chr7:770131 | T | C | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1784-340T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770131 | |||||||
| chr7:770165 | TG | T | 3 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0010c0020t0001g0011 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1784-304delG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr7 | 770165 | ||||||
| chr7:770182 | C | T | 1 | a0001c0004t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1784-289C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770182 | |||||||
| chr7:770213 | A | G | 1 | a0001c0001t0014g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1784-258A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770213 | |||||||
| chr7:770283 | T | C | 109 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1784-188T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770283 | |||||||
| chr7:770349 | G | A | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1784-122G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770349 | |||||||
| chr7:770417 | G | T | 3 | a0003c0003t0001g0111 a0003c0003t0001g0335 a0005c0007t0001g0152 |
3 | HG02615.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1784-54G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770417 | |||||||
| chr7:770418 | C | T | 3 | a0003c0003t0001g0111 a0003c0003t0001g0335 a0005c0007t0001g0152 |
3 | HG02615.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1784-53C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770418 | |||||||
| chr7:770427 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1784-44G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 8/12 | chr7 | 770427 | |||||||
| chr7:770740 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1931+122C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 770740 | |||||||
| chr7:770759 | C | G | 1 | a0003c0003t0003g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1931+141C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 770759 | |||||||
| chr7:770832 | C | T | 106 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(103): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1931+214C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 770832 | |||||||
| chr7:770869 | T | C | 231 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(228): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1931+251T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 770869 | |||||||
| chr7:770929 | C | G | 1 | a0003c0003t0005g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1931+311C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 770929 | |||||||
| chr7:770963 | C | CACAAGCT others(11): Show |
222 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1931+347_1931+364d others(20): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 770963 | ||||||
| chr7:770973 | C | CGGCAGGG others(11): Show |
1 | a0003c0003t0003g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1931+364_1931+365i others(20): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 770973 | ||||||
| chr7:770974 | G | GGCAGGGA others(11): Show |
4 | a0002c0002t0001g0236 a0002c0002t0001g0252 a0002c0002t0001g0253 others(1): Show |
4 | HG00735.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1931+364_1931+365i others(20): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 770974 | ||||||
| chr7:771016 | G | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1931+398G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771016 | |||||||
| chr7:771094 | C | G | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+476C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771094 | |||||||
| chr7:771099 | T | C | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+481T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771099 | |||||||
| chr7:771175 | A | G | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+557A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771175 | |||||||
| chr7:771203 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1931+585G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771203 | |||||||
| chr7:771204 | G | T | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+586G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771204 | |||||||
| chr7:771205 | T | G | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+587T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771205 | |||||||
| chr7:771207 | G | C | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+589G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771207 | |||||||
| chr7:771215 | A | G | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1931+597A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771215 | |||||||
| chr7:771263 | A | C | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1931+645A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771263 | |||||||
| chr7:771441 | G | A | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1931+823G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771441 | |||||||
| chr7:771477 | G | A | 60 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1931+859G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771477 | |||||||
| chr7:771647 | A | G | 4 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(1): Show |
4 | HG01978.hp1 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1931+1029A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771647 | |||||||
| chr7:771775 | G | A | 18 | a0001c0004t0001g0115 a0003c0003t0005g0256 a0003c0003t0005g0334 others(15): Show |
18 | HG01106.hp1 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1931+1157G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771775 | |||||||
| chr7:771778 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0106 a0001c0001t0004g0184 |
4 | NA19006.hp1 NA19062.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1931+1160G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771778 | |||||||
| chr7:771954 | AT | A | 129 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(126): Show |
138 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.1931+1347delT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 771954 | ||||||
| chr7:771954 | ATT | A | 8 | a0002c0002t0001g0208 a0002c0002t0001g0294 a0002c0002t0001g0296 others(5): Show |
8 | HG01167.hp2 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1931+1346_1931+134 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 771954 | ||||||
| chr7:771970 | G | A | 1 | a0002c0002t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1931+1352G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 771970 | |||||||
| chr7:772052 | C | T | 2 | a0002c0002t0001g0011 a0010c0020t0001g0011 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1931+1434C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772052 | |||||||
| chr7:772084 | G | A | 60 | a0003c0003t0003g0001 a0003c0003t0003g0002 a0003c0003t0003g0007 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1931+1466G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772084 | |||||||
| chr7:772124 | G | A | 1 | a0001c0004t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1931+1506G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772124 | |||||||
| chr7:772131 | C | G | 1 | a0003c0003t0003g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1931+1513C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772131 | |||||||
| chr7:772170 | C | G | 1 | a0001c0004t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1931+1552C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772170 | |||||||
| chr7:772292 | G | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1931+1674G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772292 | |||||||
| chr7:772426 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1932-1622C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772426 | |||||||
| chr7:772427 | G | A | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1932-1621G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772427 | |||||||
| chr7:772577 | A | G | 1 | a0001c0001t0004g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1932-1471A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772577 | |||||||
| chr7:772584 | G | GTATGAAG others(246): Show |
1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1932-1464_1932-146 others(257): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772584 | |||||||
| chr7:772585 | G | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1932-1463G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772585 | |||||||
| chr7:772589 | C | A | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1932-1459C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772589 | |||||||
| chr7:772590 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1932-1458C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772590 | |||||||
| chr7:772617 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0081 a0001c0001t0002g0087 others(1): Show |
6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932-1431G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772617 | |||||||
| chr7:772621 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1932-1427C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772621 | |||||||
| chr7:772655 | G | A | 3 | a0003c0003t0001g0111 a0003c0003t0001g0335 a0005c0007t0001g0152 |
3 | HG02615.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1932-1393G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772655 | |||||||
| chr7:772715 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1932-1333G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772715 | |||||||
| chr7:772789 | A | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1932-1259A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772789 | |||||||
| chr7:772939 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1932-1109G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772939 | |||||||
| chr7:772960 | TA | T | 141 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0003g0318 others(138): Show |
153 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1932-1069delA | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 772960 | ||||||
| chr7:772960 | TAA | T | 74 | a0001c0001t0004g0171 a0002c0002t0001g0305 a0002c0002t0001g0311 others(71): Show |
86 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1932-1070_1932-106 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 772960 | ||||||
| chr7:772962 | A | T | 1 | a0002c0002t0001g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1932-1086A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772962 | |||||||
| chr7:772979 | A | T | 1 | a0002c0002t0016g0251 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1932-1069A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772979 | |||||||
| chr7:772982 | T | A | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1932-1066T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772982 | |||||||
| chr7:772983 | A | T | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1932-1065A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 772983 | |||||||
| chr7:773009 | C | T | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1932-1039C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773009 | |||||||
| chr7:773037 | T | G | 1 | a0001c0001t0006g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1932-1011T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773037 | |||||||
| chr7:773085 | G | C | 228 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(225): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1932-963G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773085 | |||||||
| chr7:773144 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1932-904C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773144 | |||||||
| chr7:773221 | C | T | 1 | a0002c0002t0001g0244 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1932-827C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773221 | |||||||
| chr7:773236 | C | G | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1932-812C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773236 | |||||||
| chr7:773312 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1932-736C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773312 | |||||||
| chr7:773509 | G | T | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1932-539G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773509 | |||||||
| chr7:773519 | GCTGTGGC others(21): Show |
G | 7 | a0002c0002t0001g0294 a0002c0002t0001g0296 a0002c0002t0001g0297 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1932-518_1932-491d others(30): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 773519 | ||||||
| chr7:773531 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1932-517G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773531 | |||||||
| chr7:773538 | C | T | 3 | a0003c0003t0003g0190 a0003c0003t0003g0191 a0005c0007t0003g0142 |
3 | HG02630.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1932-510C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773538 | |||||||
| chr7:773568 | C | T | 1 | a0002c0002t0001g0200 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1932-480C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773568 | |||||||
| chr7:773711 | G | C | 1 | a0001c0004t0001g0049 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1932-337G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773711 | |||||||
| chr7:773741 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1932-307C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773741 | |||||||
| chr7:773970 | C | A | 1 | a0002c0002t0001g0245 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1932-78C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773970 | |||||||
| chr7:773981 | T | C | 226 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1932-67T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 773981 | |||||||
| chr7:774013 | G | A | 190 | a0001c0001t0003g0318 a0002c0002t0001g0009 a0002c0002t0001g0011 others(187): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1932-35G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 774013 | |||||||
| chr7:774016 | C | G | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1932-32C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 774016 | |||||||
| chr7:774029 | C | G | 1 | a0002c0002t0001g0245 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1932-19C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 9/12 | chr7 | 774029 | |||||||
| chr7:774230 | C | G | 194 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(191): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2082+32C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774230 | |||||||
| chr7:774306 | C | T | 4 | a0002c0002t0001g0018 a0002c0002t0001g0201 a0002c0002t0001g0215 others(1): Show |
5 | HG02886.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+108C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774306 | |||||||
| chr7:774366 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2082+168C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774366 | |||||||
| chr7:774377 | G | A | 1 | a0003c0003t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2082+179G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774377 | |||||||
| chr7:774417 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2082+219C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774417 | |||||||
| chr7:774434 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2082+236C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774434 | |||||||
| chr7:774494 | A | G | 1 | a0003c0003t0003g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2082+296A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774494 | |||||||
| chr7:774497 | C | T | 2 | a0002c0002t0001g0218 a0002c0026t0001g0211 |
2 | HG01978.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2082+299C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774497 | |||||||
| chr7:774517 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2082+319C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774517 | |||||||
| chr7:774551 | G | A | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+353G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774551 | |||||||
| chr7:774553 | CTT | C | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+357_2082+358d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr7 | 774553 | ||||||
| chr7:774556 | T | C | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+358T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774556 | |||||||
| chr7:774558 | C | A | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+360C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774558 | |||||||
| chr7:774560 | C | G | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+362C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774560 | |||||||
| chr7:774561 | A | C | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+363A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774561 | |||||||
| chr7:774562 | T | C | 98 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(95): Show |
106 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2082+364T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774562 | |||||||
| chr7:774623 | C | G | 1 | a0003c0003t0003g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2083-383C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774623 | |||||||
| chr7:774657 | C | T | 4 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(1): Show |
4 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2083-349C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774657 | |||||||
| chr7:774721 | C | T | 2 | a0003c0005t0005g0287 a0003c0005t0005g0288 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2083-285C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774721 | |||||||
| chr7:774722 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2083-284C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774722 | |||||||
| chr7:774792 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2083-214G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774792 | |||||||
| chr7:774932 | T | G | 1 | a0002c0002t0001g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2083-74T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774932 | |||||||
| chr7:774933 | G | A | 1 | a0002c0002t0001g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2083-73G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774933 | |||||||
| chr7:774952 | C | T | 1 | a0002c0002t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2083-54C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774952 | |||||||
| chr7:774975 | G | A | 198 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(195): Show |
220 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2083-31G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 10/12 | chr7 | 774975 | |||||||
| chr7:775241 | A | C | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2239+79A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775241 | |||||||
| chr7:775271 | G | T | 1 | a0003c0003t0003g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2239+109G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775271 | |||||||
| chr7:775306 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2239+144C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775306 | |||||||
| chr7:775373 | C | T | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2239+211C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775373 | |||||||
| chr7:775511 | GGT | G | 34 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(31): Show |
36 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2239+376_2239+377d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 775511 | ||||||
| chr7:775511 | GGTGT | G | 161 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(158): Show |
177 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.2239+374_2239+377d others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 775511 | ||||||
| chr7:775511 | GGTGTGT | G | 67 | a0003c0003t0001g0111 a0003c0003t0001g0192 a0003c0003t0003g0001 others(64): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.2239+372_2239+377d others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 775511 | ||||||
| chr7:775513 | T | G | 1 | a0001c0004t0001g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2239+351T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775513 | |||||||
| chr7:775646 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2239+484C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775646 | |||||||
| chr7:775685 | A | G | 9 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2239+523A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775685 | |||||||
| chr7:775728 | C | A | 1 | a0001c0001t0004g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2239+566C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775728 | |||||||
| chr7:775744 | T | G | 7 | a0001c0001t0002g0028 a0001c0001t0002g0319 a0001c0001t0002g0320 others(4): Show |
8 | NA18612.hp2 NA18955.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2239+582T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775744 | |||||||
| chr7:775754 | G | A | 5 | a0002c0002t0001g0203 a0002c0002t0001g0279 a0002c0002t0001g0280 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2239+592G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775754 | |||||||
| chr7:775777 | T | A | 1 | a0002c0002t0001g0279 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2239+615T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775777 | |||||||
| chr7:775786 | G | A | 2 | a0003c0003t0001g0111 a0003c0003t0001g0335 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2239+624G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775786 | |||||||
| chr7:775844 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2239+682G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775844 | |||||||
| chr7:775879 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2239+717G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 775879 | |||||||
| chr7:776012 | T | A | 190 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(187): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2239+850T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776012 | |||||||
| chr7:776089 | C | T | 1 | a0001c0004t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2239+927C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776089 | |||||||
| chr7:776207 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2239+1045G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776207 | |||||||
| chr7:776422 | C | T | 61 | a0003c0003t0001g0192 a0003c0003t0003g0001 a0003c0003t0003g0002 others(58): Show |
75 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.2239+1260C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776422 | |||||||
| chr7:776551 | T | TG | 110 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(107): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2239+1393dupG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 776551 | ||||||
| chr7:776607 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2239+1445G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776607 | |||||||
| chr7:776637 | A | T | 9 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2239+1475A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776637 | |||||||
| chr7:776720 | A | G | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2239+1558A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776720 | |||||||
| chr7:776782 | C | T | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2239+1620C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776782 | |||||||
| chr7:776860 | A | G | 199 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(196): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2239+1698A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776860 | |||||||
| chr7:776970 | C | T | 190 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(187): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2239+1808C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 776970 | |||||||
| chr7:777001 | A | G | 277 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0063 others(274): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2239+1839A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777001 | |||||||
| chr7:777069 | C | T | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2239+1907C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777069 | |||||||
| chr7:777208 | A | G | 190 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(187): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2239+2046A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777208 | |||||||
| chr7:777335 | G | A | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2239+2173G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777335 | |||||||
| chr7:777564 | A | G | 264 | a0001c0001t0002g0012 a0001c0001t0002g0092 a0001c0001t0003g0318 others(261): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2240-2389A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777564 | |||||||
| chr7:777582 | G | A | 3 | a0002c0002t0001g0222 a0002c0002t0001g0223 a0002c0002t0001g0264 |
3 | HG00323.hp1 HG00642.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2240-2371G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777582 | |||||||
| chr7:777593 | A | G | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2240-2360A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777593 | |||||||
| chr7:777666 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2240-2287C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777666 | |||||||
| chr7:777697 | C | T | 190 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(187): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2240-2256C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777697 | |||||||
| chr7:777754 | T | C | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2240-2199T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777754 | |||||||
| chr7:777818 | G | A | 190 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(187): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2240-2135G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777818 | |||||||
| chr7:777851 | G | A | 1 | a0001c0004t0001g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2240-2102G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777851 | |||||||
| chr7:777889 | G | A | 1 | a0001c0001t0004g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2240-2064G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777889 | |||||||
| chr7:777959 | G | A | 1 | a0003c0005t0005g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2240-1994G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777959 | |||||||
| chr7:777994 | C | T | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2240-1959C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 777994 | |||||||
| chr7:778000 | G | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2240-1953G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778000 | |||||||
| chr7:778046 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2240-1907C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778046 | |||||||
| chr7:778061 | G | A | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | NA18981.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2240-1892G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778061 | |||||||
| chr7:778084 | CG | C | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2240-1864delG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 778084 | ||||||
| chr7:778243 | G | C | 2 | a0003c0003t0007g0101 a0003c0003t0007g0102 |
2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2240-1710G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778243 | |||||||
| chr7:778260 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2240-1693C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778260 | |||||||
| chr7:778300 | T | C | 1 | a0001c0001t0004g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2240-1653T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778300 | |||||||
| chr7:778320 | G | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2240-1633G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778320 | |||||||
| chr7:778370 | A | G | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2240-1583A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778370 | |||||||
| chr7:778441 | GGACA | G | 9 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2240-1503_2240-150 others(8): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 778441 | ||||||
| chr7:778486 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2240-1467C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778486 | |||||||
| chr7:778487 | G | A | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2240-1466G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778487 | |||||||
| chr7:778597 | CTG | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2240-1352_2240-135 others(6): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 778597 | ||||||
| chr7:778615 | G | A | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2240-1338G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778615 | |||||||
| chr7:778618 | C | T | 2 | a0002c0002t0001g0239 a0002c0002t0001g0240 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2240-1335C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778618 | |||||||
| chr7:778636 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2240-1317C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778636 | |||||||
| chr7:778695 | G | A | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | NA18981.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2240-1258G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778695 | |||||||
| chr7:778732 | C | T | 1 | a0017c0029t0010g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2240-1221C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778732 | |||||||
| chr7:778733 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2240-1220G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778733 | |||||||
| chr7:778755 | G | C | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2240-1198G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778755 | |||||||
| chr7:778762 | C | T | 1 | a0001c0004t0001g0051 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2240-1191C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778762 | |||||||
| chr7:778763 | G | A | 1 | a0002c0002t0001g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2240-1190G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778763 | |||||||
| chr7:778875 | G | A | 2 | a0002c0002t0001g0218 a0002c0026t0001g0211 |
2 | HG01978.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2240-1078G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778875 | |||||||
| chr7:778906 | G | A | 9 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2240-1047G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778906 | |||||||
| chr7:778932 | C | G | 1 | a0003c0003t0003g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2240-1021C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 778932 | |||||||
| chr7:779035 | G | C | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2240-918G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779035 | |||||||
| chr7:779127 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2240-826C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779127 | |||||||
| chr7:779186 | G | A | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2240-767G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779186 | |||||||
| chr7:779519 | G | C | 1 | a0003c0003t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2240-434G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779519 | |||||||
| chr7:779564 | A | T | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2240-389A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779564 | |||||||
| chr7:779587 | C | T | 105 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(102): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2240-366C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779587 | |||||||
| chr7:779588 | G | A | 1 | a0001c0001t0004g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2240-365G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779588 | |||||||
| chr7:779698 | C | T | 1 | a0003c0005t0005g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2240-255C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779698 | |||||||
| chr7:779840 | T | C | 233 | a0001c0001t0003g0318 a0001c0001t0004g0023 a0001c0001t0004g0024 others(230): Show |
257 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.2240-113T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779840 | |||||||
| chr7:779908 | A | G | 1 | a0001c0004t0001g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2240-45A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779908 | |||||||
| chr7:779941 | C | T | 2 | a0003c0005t0005g0209 a0003c0005t0005g0210 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2240-12C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 11/12 | chr7 | 779941 | |||||||
| chr7:780226 | C | G | 9 | a0002c0002t0001g0203 a0002c0002t0001g0235 a0002c0002t0001g0246 others(6): Show |
9 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2431+82C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780226 | |||||||
| chr7:780226 | C | T | 1 | a0015c0027t0003g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2431+82C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780226 | |||||||
| chr7:780265 | C | T | 1 | a0017c0029t0010g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2431+121C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780265 | |||||||
| chr7:780368 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2431+224C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780368 | |||||||
| chr7:780385 | T | A | 1 | a0002c0002t0001g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2431+241T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780385 | |||||||
| chr7:780441 | T | C | 1 | a0001c0001t0004g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2431+297T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780441 | |||||||
| chr7:780474 | A | C | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2431+330A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780474 | |||||||
| chr7:780475 | G | T | 1 | a0003c0003t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2431+331G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780475 | |||||||
| chr7:780508 | T | G | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2431+364T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780508 | |||||||
| chr7:780660 | G | A | 1 | a0002c0002t0001g0268 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2431+516G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780660 | |||||||
| chr7:780815 | CT | C | 60 | a0002c0002t0003g0272 a0003c0003t0003g0001 a0003c0003t0003g0002 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.2431+681delT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 780815 | ||||||
| chr7:780825 | T | C | 1 | a0003c0003t0003g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2431+681T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780825 | |||||||
| chr7:780826 | C | T | 4 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2431+682C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780826 | |||||||
| chr7:780826 | CTT | C | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2431+695_2431+696d others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 780826 | ||||||
| chr7:780836 | T | G | 6 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(3): Show |
6 | HG01074.hp2 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2431+692T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780836 | |||||||
| chr7:780841 | G | T | 1 | a0002c0002t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2431+697G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780841 | |||||||
| chr7:780889 | T | C | 26 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.2431+745T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780889 | |||||||
| chr7:780922 | A | AG | 120 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(117): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.2431+778_2431+779i others(3): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 780922 | |||||||
| chr7:781164 | C | T | 137 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(134): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.2431+1020C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781164 | |||||||
| chr7:781175 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2431+1031G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781175 | |||||||
| chr7:781194 | G | C | 1 | a0003c0003t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2431+1050G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781194 | |||||||
| chr7:781272 | C | T | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2431+1128C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781272 | |||||||
| chr7:781315 | C | T | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2431+1171C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781315 | |||||||
| chr7:781372 | G | A | 1 | a0002c0008t0001g0277 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2431+1228G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781372 | |||||||
| chr7:781375 | T | A | 1 | a0002c0002t0001g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2431+1231T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781375 | |||||||
| chr7:781377 | A | C | 1 | a0002c0002t0001g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2431+1233A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781377 | |||||||
| chr7:781389 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2431+1245G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781389 | |||||||
| chr7:781399 | C | A | 1 | a0003c0003t0001g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2431+1255C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781399 | |||||||
| chr7:781425 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2431+1281G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781425 | |||||||
| chr7:781483 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2431+1339C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781483 | |||||||
| chr7:781486 | G | A | 81 | a0001c0001t0003g0318 a0002c0002t0003g0272 a0003c0003t0003g0001 others(78): Show |
95 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.2431+1342G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781486 | |||||||
| chr7:781548 | C | G | 1 | a0002c0002t0001g0283 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2431+1404C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781548 | |||||||
| chr7:781564 | C | CT | 27 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(24): Show |
29 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2431+1421dupT | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 781564 | ||||||
| chr7:781598 | C | CTCCCAGC others(15): Show |
1 | a0001c0001t0002g0030 | 2 | NA18968.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2431+1460_2431+148 others(26): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 781598 | ||||||
| chr7:781606 | G | GGTGCTCA others(15): Show |
9 | a0002c0002t0001g0206 a0002c0002t0001g0222 a0002c0002t0001g0223 others(6): Show |
9 | HG00323.hp1 HG00642.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.2431+1464_2431+148 others(26): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 781606 | ||||||
| chr7:781742 | G | A | 3 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0016g0251 |
3 | HG01192.hp2 HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2431+1598G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781742 | |||||||
| chr7:781746 | G | C | 109 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0018 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2431+1602G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781746 | |||||||
| chr7:781787 | C | T | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0090 others(10): Show |
14 | HG00544.hp1 HG00621.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.2431+1643C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781787 | |||||||
| chr7:781805 | C | G | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2431+1661C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781805 | |||||||
| chr7:781951 | C | T | 8 | a0003c0003t0003g0008 a0003c0003t0003g0126 a0003c0003t0003g0135 others(5): Show |
10 | HG00558.hp1 HG02040.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.2431+1807C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781951 | |||||||
| chr7:781956 | G | A | 1 | a0002c0002t0001g0268 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2431+1812G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 781956 | |||||||
| chr7:782059 | G | C | 1 | a0003c0005t0005g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2431+1915G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782059 | |||||||
| chr7:782078 | C | T | 2 | a0002c0017t0001g0302 a0002c0025t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2431+1934C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782078 | |||||||
| chr7:782097 | G | C | 2 | a0004c0006t0001g0010 a0004c0006t0001g0309 |
4 | NA18964.hp2 NA18983.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.2431+1953G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782097 | |||||||
| chr7:782105 | G | A | 1 | a0016c0028t0004g0173 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2431+1961G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782105 | |||||||
| chr7:782117 | T | TGTGGCCG others(87): Show |
100 | a0002c0002t0001g0009 a0002c0002t0001g0018 a0002c0002t0001g0025 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2431+2016_2431+201 others(98): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782117 | ||||||
| chr7:782138 | A | AGCGTCAG others(87): Show |
1 | a0006c0011t0001g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2431+2016_2431+201 others(98): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782138 | ||||||
| chr7:782161 | C | T | 217 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(214): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2431+2017C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782161 | |||||||
| chr7:782170 | C | CGCCTCCC others(40): Show |
2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2431+2034_2431+203 others(51): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782170 | ||||||
| chr7:782170 | C | G | 77 | a0002c0002t0003g0272 a0003c0003t0003g0001 a0003c0003t0003g0002 others(74): Show |
91 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.2431+2026C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782170 | |||||||
| chr7:782179 | A | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2035A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782179 | |||||||
| chr7:782181 | A | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2037A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782181 | |||||||
| chr7:782185 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2041G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782185 | |||||||
| chr7:782197 | T | TCGGATCT others(85): Show |
1 | a0002c0026t0001g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2431+2087_2431+208 others(96): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782197 | ||||||
| chr7:782199 | G | A | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2431+2055G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782199 | |||||||
| chr7:782207 | C | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2063C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782207 | |||||||
| chr7:782216 | C | A | 1 | a0003c0003t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2431+2072C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782216 | |||||||
| chr7:782217 | C | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2073C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782217 | |||||||
| chr7:782224 | C | T | 1 | a0003c0003t0003g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2431+2080C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782224 | |||||||
| chr7:782226 | T | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2082T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782226 | |||||||
| chr7:782228 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2084G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782228 | |||||||
| chr7:782232 | G | A | 4 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 others(1): Show |
4 | HG02109.hp1 HG02155.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2431+2088G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782232 | |||||||
| chr7:782254 | G | A | 60 | a0002c0002t0003g0272 a0003c0003t0003g0001 a0003c0003t0003g0002 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.2431+2110G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782254 | |||||||
| chr7:782254 | G | C | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2110G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782254 | |||||||
| chr7:782255 | C | T | 5 | a0001c0001t0003g0318 a0002c0002t0001g0243 a0002c0002t0001g0273 others(2): Show |
5 | HG02109.hp1 HG02155.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.2431+2111C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782255 | |||||||
| chr7:782265 | A | G | 4 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 others(1): Show |
4 | HG02109.hp1 HG02155.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2431+2121A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782265 | |||||||
| chr7:782273 | A | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2129A>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782273 | |||||||
| chr7:782275 | A | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2131A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782275 | |||||||
| chr7:782282 | A | G | 7 | a0001c0001t0003g0318 a0001c0024t0011g0041 a0002c0002t0001g0243 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.2431+2138A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782282 | |||||||
| chr7:782301 | C | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2157C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782301 | |||||||
| chr7:782302 | T | C | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2158T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782302 | |||||||
| chr7:782312 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2168G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782312 | |||||||
| chr7:782319 | G | A | 2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2431+2175G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782319 | |||||||
| chr7:782320 | T | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2176T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782320 | |||||||
| chr7:782322 | A | G | 4 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 others(1): Show |
4 | HG02109.hp1 HG02155.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2431+2178A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782322 | |||||||
| chr7:782326 | G | A | 8 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2431+2182G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782326 | |||||||
| chr7:782329 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2185G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782329 | |||||||
| chr7:782342 | C | A | 6 | a0001c0001t0003g0318 a0001c0024t0011g0041 a0002c0002t0001g0243 others(3): Show |
6 | HG02109.hp1 HG02155.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2431+2198C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782342 | |||||||
| chr7:782348 | G | C | 2 | a0001c0001t0003g0318 a0001c0024t0011g0041 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2431+2204G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782348 | |||||||
| chr7:782348 | G | GCGGCGTG others(40): Show |
1 | a0002c0002t0016g0251 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2431+2222_2431+226 others(51): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782348 | ||||||
| chr7:782349 | C | T | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2205C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782349 | |||||||
| chr7:782352 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2431+2208C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782352 | |||||||
| chr7:782359 | G | A | 3 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 |
3 | HG02155.hp2 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2431+2215G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782359 | |||||||
| chr7:782367 | T | A | 4 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 others(1): Show |
4 | HG02109.hp1 HG02155.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2431+2223T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782367 | |||||||
| chr7:782376 | G | A | 3 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 |
3 | HG02155.hp2 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2431+2232G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782376 | |||||||
| chr7:782388 | C | G | 5 | a0001c0001t0003g0318 a0002c0002t0001g0243 a0002c0002t0001g0273 others(2): Show |
5 | HG02109.hp1 HG02155.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.2431+2244C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782388 | |||||||
| chr7:782389 | A | C | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2245A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782389 | |||||||
| chr7:782395 | C | CCGGCGTG others(181): Show |
2 | a0011c0018t0010g0120 a0017c0029t0010g0119 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2431+2268_2431+226 others(192): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782395 | ||||||
| chr7:782395 | C | CTGGCGTG others(40): Show |
1 | a0002c0002t0001g0286 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2431+2251_2431+225 others(51): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782395 | |||||||
| chr7:782395 | C | G | 1 | a0001c0001t0003g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2431+2251C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782395 | |||||||
| chr7:782396 | C | T | 3 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 |
3 | HG02155.hp2 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2431+2252C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782396 | |||||||
| chr7:782397 | G | A | 1 | a0003c0003t0003g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2431+2253G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782397 | |||||||
| chr7:782399 | CGTGGCCG others(40): Show |
C | 3 | a0002c0002t0001g0011 a0003c0003t0003g0020 a0010c0020t0001g0011 |
4 | HG02258.hp2 HG02818.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.2431+2269_2431+231 others(51): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782399 | ||||||
| chr7:782410 | C | A | 11 | a0001c0001t0006g0065 a0001c0001t0006g0071 a0001c0001t0006g0073 others(8): Show |
11 | HG00558.hp2 HG02015.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2431+2266C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782410 | |||||||
| chr7:782413 | C | G | 225 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(222): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2431+2269C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782413 | |||||||
| chr7:782415 | C | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2431+2271C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782415 | |||||||
| chr7:782419 | C | T | 2 | a0003c0003t0003g0113 a0003c0003t0003g0114 |
2 | NA19055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2431+2275C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782419 | |||||||
| chr7:782435 | C | CATCTTCC others(87): Show |
2 | a0002c0017t0001g0302 a0002c0025t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2431+2298_2431+229 others(98): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782435 | ||||||
| chr7:782435 | C | G | 1 | a0002c0002t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2431+2291C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782435 | |||||||
| chr7:782435 | CATCTTCC others(318): Show |
C | 5 | a0003c0003t0001g0111 a0003c0003t0001g0192 a0003c0003t0001g0335 others(2): Show |
5 | HG01496.hp2 HG02615.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2431+2302_2431+262 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782435 | ||||||
| chr7:782436 | A | C | 1 | a0002c0002t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2431+2292A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782436 | |||||||
| chr7:782442 | C | G | 1 | a0002c0002t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2431+2298C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782442 | |||||||
| chr7:782443 | T | C | 222 | a0001c0001t0003g0318 a0001c0001t0004g0313 a0001c0001t0004g0314 others(219): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.2431+2299T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782443 | |||||||
| chr7:782446 | T | C | 219 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(216): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2431+2302T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782446 | |||||||
| chr7:782482 | G | C | 222 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2431+2338G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782482 | |||||||
| chr7:782490 | C | T | 207 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(204): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2431+2346C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782490 | |||||||
| chr7:782493 | C | T | 206 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(203): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2431+2349C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782493 | |||||||
| chr7:782502 | G | C | 222 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2431+2358G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782502 | |||||||
| chr7:782502 | GTCCCGTC others(133): Show |
G | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2431+2370_2431+250 others(4): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782502 | ||||||
| chr7:782529 | C | G | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2385C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782529 | |||||||
| chr7:782537 | T | C | 213 | a0001c0001t0004g0165 a0001c0004t0001g0004 a0001c0004t0001g0031 others(210): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2431+2393T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782537 | |||||||
| chr7:782540 | T | C | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2396T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782540 | |||||||
| chr7:782549 | C | G | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2405C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782549 | |||||||
| chr7:782576 | G | C | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2432G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782576 | |||||||
| chr7:782584 | C | T | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2440C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782584 | |||||||
| chr7:782584 | CGGCGTGG others(39): Show |
C | 1 | a0001c0001t0002g0081 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2431+2452_2431+249 others(50): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782584 | ||||||
| chr7:782587 | C | T | 235 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(232): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2431+2443C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782587 | |||||||
| chr7:782596 | G | C | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2452G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782596 | |||||||
| chr7:782603 | T | C | 222 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2431+2459T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782603 | |||||||
| chr7:782608 | A | G | 163 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(160): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2431+2464A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782608 | |||||||
| chr7:782621 | C | CG | 208 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(205): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2431+2478dupG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782621 | ||||||
| chr7:782622 | G | GC | 12 | a0001c0001t0003g0318 a0002c0002t0001g0011 a0002c0002t0001g0243 others(9): Show |
13 | HG02109.hp1 HG02155.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2431+2478_2431+247 others(5): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782622 | |||||||
| chr7:782625 | A | C | 222 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2431+2481A>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782625 | |||||||
| chr7:782625 | ATTCCTGG others(39): Show |
A | 29 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(26): Show |
31 | HG00621.hp1 HG01884.hp1 HG02132.hp1 others(28): Show |
intron_variant | MODIFIER | c.2431+2617_2431+266 others(50): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782625 | ||||||
| chr7:782630 | T | C | 211 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(208): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2431+2486T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782630 | |||||||
| chr7:782633 | C | T | 12 | a0001c0001t0003g0318 a0002c0002t0001g0011 a0002c0002t0001g0243 others(9): Show |
13 | HG02109.hp1 HG02155.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2431+2489C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782633 | |||||||
| chr7:782642 | C | G | 210 | a0001c0004t0001g0004 a0001c0004t0001g0031 a0001c0004t0001g0032 others(207): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2431+2498C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782642 | |||||||
| chr7:782649 | C | CACGCGGC others(40): Show |
6 | a0002c0002t0001g0243 a0002c0002t0001g0273 a0002c0002t0001g0275 others(3): Show |
6 | HG02109.hp1 HG02155.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2431+2509_2431+251 others(51): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782649 | ||||||
| chr7:782649 | C | T | 213 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(210): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2431+2505C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782649 | |||||||
| chr7:782654 | A | G | 6 | a0001c0001t0003g0318 a0002c0002t0001g0011 a0002c0002t0001g0201 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2431+2510A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782654 | |||||||
| chr7:782665 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2431+2521C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782665 | |||||||
| chr7:782667 | C | CG | 4 | a0001c0001t0003g0318 a0003c0003t0003g0020 a0011c0018t0010g0120 others(1): Show |
5 | HG02280.hp2 HG03490.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.2431+2524dupG | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 782667 | ||||||
| chr7:782671 | C | A | 220 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2431+2527C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782671 | |||||||
| chr7:782676 | T | C | 4 | a0001c0001t0003g0318 a0003c0003t0003g0020 a0011c0018t0010g0120 others(1): Show |
5 | HG02280.hp2 HG03490.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.2431+2532T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782676 | |||||||
| chr7:782688 | C | G | 6 | a0001c0001t0003g0318 a0002c0002t0001g0011 a0003c0003t0003g0020 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2431+2544C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782688 | |||||||
| chr7:782695 | C | T | 6 | a0001c0001t0003g0318 a0002c0002t0001g0011 a0003c0003t0003g0020 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2431+2551C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782695 | |||||||
| chr7:782717 | C | A | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2431+2573C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782717 | |||||||
| chr7:782756 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2431+2612A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782756 | |||||||
| chr7:782785 | G | A | 1 | a0001c0024t0011g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2431+2641G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782785 | |||||||
| chr7:782834 | C | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2432-2683C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782834 | |||||||
| chr7:782834 | C | T | 1 | a0016c0028t0004g0173 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2432-2683C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782834 | |||||||
| chr7:782837 | C | T | 1 | a0002c0002t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2432-2680C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782837 | |||||||
| chr7:782858 | T | C | 1 | a0002c0002t0001g0266 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2432-2659T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782858 | |||||||
| chr7:782864 | C | T | 60 | a0002c0002t0003g0272 a0003c0003t0003g0001 a0003c0003t0003g0002 others(57): Show |
74 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.2432-2653C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782864 | |||||||
| chr7:782886 | A | G | 231 | a0001c0001t0003g0318 a0001c0001t0004g0157 a0001c0001t0004g0158 others(228): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2432-2631A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782886 | |||||||
| chr7:782911 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2432-2606G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782911 | |||||||
| chr7:782914 | G | A | 1 | a0003c0003t0003g0020 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2432-2603G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782914 | |||||||
| chr7:782928 | G | C | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2432-2589G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782928 | |||||||
| chr7:782979 | C | T | 5 | a0003c0003t0001g0111 a0003c0003t0001g0192 a0003c0003t0001g0335 others(2): Show |
5 | HG01496.hp2 HG02615.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2432-2538C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 782979 | |||||||
| chr7:783002 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2432-2515C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783002 | |||||||
| chr7:783021 | C | T | 3 | a0001c0001t0003g0318 a0011c0018t0010g0120 a0017c0029t0010g0119 |
3 | HG02280.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2432-2496C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783021 | |||||||
| chr7:783056 | G | A | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2432-2461G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783056 | |||||||
| chr7:783075 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2432-2442C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783075 | |||||||
| chr7:783114 | C | G | 1 | a0002c0002t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2432-2403C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783114 | |||||||
| chr7:783264 | C | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2432-2253C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783264 | |||||||
| chr7:783287 | G | A | 1 | a0003c0003t0003g0143 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2432-2230G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783287 | |||||||
| chr7:783311 | T | C | 1 | a0002c0002t0001g0264 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2432-2206T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783311 | |||||||
| chr7:783321 | A | G | 221 | a0001c0001t0002g0306 a0001c0001t0003g0318 a0001c0004t0001g0004 others(218): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.2432-2196A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783321 | |||||||
| chr7:783348 | T | C | 2 | a0001c0001t0006g0076 a0001c0001t0006g0077 |
2 | HG00558.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2432-2169T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783348 | |||||||
| chr7:783379 | C | T | 2 | a0001c0001t0002g0085 a0001c0001t0002g0086 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2432-2138C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783379 | |||||||
| chr7:783430 | G | C | 229 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0081 others(226): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2432-2087G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783430 | |||||||
| chr7:783434 | G | A | 1 | a0001c0001t0006g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2432-2083G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783434 | |||||||
| chr7:783472 | G | T | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | NA18981.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2432-2045G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783472 | |||||||
| chr7:783504 | T | G | 2 | a0002c0002t0001g0239 a0002c0002t0001g0240 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2432-2013T>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783504 | |||||||
| chr7:783566 | C | T | 221 | a0001c0001t0002g0306 a0001c0001t0003g0318 a0001c0004t0001g0004 others(218): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.2432-1951C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783566 | |||||||
| chr7:783570 | T | C | 1 | a0001c0016t0012g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2432-1947T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783570 | |||||||
| chr7:783577 | A | G | 1 | a0003c0003t0003g0114 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2432-1940A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783577 | |||||||
| chr7:783578 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0078 a0001c0001t0002g0083 |
4 | HG01346.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2432-1939C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783578 | |||||||
| chr7:783690 | C | G | 3 | a0003c0003t0004g0109 a0003c0003t0007g0231 a0003c0003t0007g0232 |
3 | HG01891.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2432-1827C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783690 | |||||||
| chr7:783712 | C | T | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2432-1805C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783712 | |||||||
| chr7:783728 | C | T | 1 | a0002c0002t0001g0274 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2432-1789C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783728 | |||||||
| chr7:783797 | C | A | 1 | a0001c0001t0002g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2432-1720C>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783797 | |||||||
| chr7:783815 | C | G | 1 | a0017c0029t0010g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2432-1702C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783815 | |||||||
| chr7:783829 | C | G | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2432-1688C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783829 | |||||||
| chr7:783934 | A | G | 1 | a0001c0004t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2432-1583A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 783934 | |||||||
| chr7:784014 | C | T | 1 | a0004c0006t0001g0221 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2432-1503C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784014 | |||||||
| chr7:784018 | GCCCCCAC others(2): Show |
G | 257 | a0001c0001t0002g0005 a0001c0001t0002g0066 a0001c0001t0002g0069 others(254): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2432-1481_2432-147 others(13): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 784018 | ||||||
| chr7:784124 | T | C | 229 | a0001c0001t0002g0306 a0001c0001t0003g0318 a0001c0004t0001g0004 others(226): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2432-1393T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784124 | |||||||
| chr7:784138 | T | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2432-1379T>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784138 | |||||||
| chr7:784184 | C | T | 4 | a0001c0004t0001g0032 a0001c0004t0001g0037 a0001c0004t0001g0038 others(1): Show |
4 | HG01099.hp1 HG01255.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2432-1333C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784184 | |||||||
| chr7:784197 | C | T | 109 | a0001c0001t0002g0306 a0002c0002t0001g0009 a0002c0002t0001g0011 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2432-1320C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784197 | |||||||
| chr7:784214 | G | T | 1 | a0003c0012t0004g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2432-1303G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784214 | |||||||
| chr7:784230 | C | T | 8 | a0003c0003t0003g0008 a0003c0003t0003g0126 a0003c0003t0003g0135 others(5): Show |
10 | HG00558.hp1 HG02040.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.2432-1287C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784230 | |||||||
| chr7:784251 | C | T | 2 | a0001c0001t0006g0071 a0001c0001t0006g0073 |
2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.2432-1266C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784251 | |||||||
| chr7:784334 | C | T | 1 | a0002c0002t0001g0245 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2432-1183C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784334 | |||||||
| chr7:784350 | A | AC | 24 | a0001c0001t0002g0058 a0001c0001t0002g0061 a0001c0001t0002g0323 others(21): Show |
24 | HG00621.hp1 HG00642.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.2432-1161dupC | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 784350 | ||||||
| chr7:784372 | C | T | 2 | a0003c0003t0003g0116 a0003c0003t0003g0117 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2432-1145C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784372 | |||||||
| chr7:784426 | G | A | 3 | a0001c0001t0004g0313 a0001c0001t0004g0314 a0001c0001t0004g0315 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2432-1091G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784426 | |||||||
| chr7:784648 | G | A | 4 | a0002c0002t0001g0009 a0002c0002t0001g0182 a0002c0002t0001g0268 others(1): Show |
6 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2432-869G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784648 | |||||||
| chr7:784893 | G | C | 1 | a0003c0003t0003g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2432-624G>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784893 | |||||||
| chr7:784992 | C | G | 1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2432-525C>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784992 | |||||||
| chr7:784994 | C | T | 1 | a0003c0003t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2432-523C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 784994 | |||||||
| chr7:785009 | C | T | 1 | a0003c0003t0003g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2432-508C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785009 | |||||||
| chr7:785083 | C | T | 11 | a0001c0001t0006g0065 a0001c0001t0006g0071 a0001c0001t0006g0073 others(8): Show |
11 | HG00558.hp2 HG02015.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2432-434C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785083 | |||||||
| chr7:785085 | G | T | 11 | a0001c0001t0006g0065 a0001c0001t0006g0071 a0001c0001t0006g0073 others(8): Show |
11 | HG00558.hp2 HG02015.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2432-432G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785085 | |||||||
| chr7:785092 | C | T | 1 | a0002c0002t0001g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2432-425C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785092 | |||||||
| chr7:785122 | G | A | 3 | a0001c0001t0004g0024 a0001c0001t0004g0107 a0001c0001t0004g0171 |
4 | NA18979.hp1 NA19005.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2432-395G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785122 | |||||||
| chr7:785201 | C | T | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2432-316C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785201 | |||||||
| chr7:785223 | GGTCCCCA others(70): Show |
G | 26 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0106 others(23): Show |
28 | HG00621.hp1 HG02132.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.2432-258_2432-182d others(79): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 785223 | ||||||
| chr7:785224 | G | A | 9 | a0003c0003t0004g0109 a0003c0003t0007g0101 a0003c0003t0007g0102 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2432-293G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785224 | |||||||
| chr7:785269 | C | T | 1 | a0003c0003t0003g0129 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2432-248C>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785269 | |||||||
| chr7:785285 | ACATTGTG others(70): Show |
A | 1 | a0001c0001t0002g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2432-216_2432-140d others(79): Show |
DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr7 | 785285 | ||||||
| chr7:785290 | G | T | 7 | a0002c0002t0001g0294 a0002c0002t0001g0296 a0002c0002t0001g0297 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432-227G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785290 | |||||||
| chr7:785325 | A | G | 1 | a0002c0002t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2432-192A>G | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785325 | |||||||
| chr7:785362 | G | A | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2432-155G>A | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785362 | |||||||
| chr7:785368 | T | C | 17 | a0003c0003t0005g0256 a0003c0003t0005g0334 a0003c0005t0005g0209 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2432-149T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785368 | |||||||
| chr7:785455 | G | T | 1 | a0004c0006t0001g0309 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2432-62G>T | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785455 | |||||||
| chr7:785477 | T | C | 215 | a0001c0001t0003g0318 a0001c0004t0001g0004 a0001c0004t0001g0031 others(212): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2432-40T>C | DNAAF5 | ENSG00000164818.16 | transcript | ENST00000297440.11 | protein_coding | 12/12 | chr7 | 785477 |