Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 651746 |
| ensemblid | ENSG00000164236.12 |
| hgncid | 35240 |
| symbol | ANKRD33B |
| name | ankyrin repeat domain 33B |
| refseq_nuc | NM_001164440.2 |
| refseq_prot | NP_001157912.1 |
| ensembl_nuc | ENST00000296657.7 |
| ensembl_prot | ENSP00000296657.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 10564070 |
| end | 10657816 |
| strand | + |
| ver | v1.2 |
| region | chr5:10564070-10657816 |
| region5000 | chr5:10559070-10662816 |
| regionname0 | ANKRD33B_chr5_10564070_10657816 |
| regionname5000 | ANKRD33B_chr5_10559070_10662816 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 494 | 297 | 65 | 64 | 114 | 12 | 40 | 76 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0002 | 0/0 | 494 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0003 | 0/0 | 494 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0004 | 0/0 | 494 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0005 | 0/0 | 494 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0006 | 0/0 | 494 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0007 | 0/0 | 494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0008 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0009 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| a0010 | 0/0 | 494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | MVLLA others(489): Show |
chr5 | 10559070 | 10662816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1482 | 141 | 34 | 29 | 57 | 6 | 15 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0002 | 0/1 | 1482 | 57 | 9 | 10 | 21 | 3 | 13 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0003 | 0/0 | 1482 | 27 | 0 | 3 | 21 | 0 | 3 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0004 | 0/0 | 1482 | 18 | 0 | 11 | 0 | 2 | 5 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0005 | 0/0 | 1482 | 15 | 0 | 8 | 3 | 1 | 3 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0006 | 0/0 | 1482 | 6 | 0 | 1 | 4 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0007 | 0/0 | 1482 | 6 | 0 | 0 | 6 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0009 | 0/0 | 1482 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0011 | 1/0 | 1482 | 3 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0013 | 0/0 | 1482 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0014 | 0/0 | 1482 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0015 | 0/0 | 1482 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0020 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0021 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0023 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0024 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0025 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0026 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0030 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0031 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0033 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0034 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0001c0037 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0002c0010 | 0/0 | 1482 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0002c0012 | 0/0 | 1482 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0002c0028 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0003c0016 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0003c0019 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0003c0035 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0004c0008 | 0/0 | 1482 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0005c0017 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0005c0027 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0006c0018 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0007c0022 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0008c0036 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0009c0032 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 | ||
| a0010c0029 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | ATGGT others(1477): Show |
chr5 | 10559070 | 10662816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9586 | 70 | 12 | 12 | 30 | 5 | 11 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0004 | 0/0 | 9586 | 5 | 0 | 0 | 4 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0005 | 0/0 | 9582 | 11 | 0 | 0 | 11 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0006 | 0/0 | 9586 | 11 | 10 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0009 | 0/0 | 9586 | 6 | 0 | 4 | 1 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0012 | 0/0 | 9584 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9579): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0013 | 0/0 | 9586 | 4 | 0 | 4 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0024 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0025 | 0/0 | 9586 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0026 | 0/0 | 9588 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0027 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0029 | 0/0 | 9586 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0031 | 0/0 | 9582 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0032 | 0/0 | 9586 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0033 | 0/0 | 9586 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0042 | 0/0 | 9586 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0045 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0047 | 0/0 | 9587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9582): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0048 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0049 | 0/0 | 9586 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0051 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0052 | 0/0 | 9588 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0054 | 0/0 | 9586 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0055 | 0/0 | 9586 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0056 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0057 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0059 | 0/0 | 9584 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9579): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0065 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0066 | 0/0 | 9586 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0067 | 0/0 | 9586 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0001t0068 | 0/0 | 9598 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9593): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0001 | 0/1 | 9586 | 40 | 5 | 5 | 15 | 3 | 11 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0004 | 0/0 | 9586 | 6 | 1 | 0 | 5 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0006 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0016 | 0/0 | 9586 | 3 | 0 | 3 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0027 | 0/0 | 9586 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0030 | 0/0 | 9586 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0043 | 0/0 | 9588 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0046 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0050 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0002t0053 | 0/0 | 9584 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9579): Show |
chr5 | 10559070 | 10662816 |
| a0001c0003t0003 | 0/0 | 9581 | 15 | 0 | 3 | 12 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0003t0007 | 0/0 | 9580 | 6 | 0 | 0 | 4 | 0 | 2 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9575): Show |
chr5 | 10559070 | 10662816 |
| a0001c0003t0017 | 0/0 | 9580 | 3 | 0 | 0 | 2 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9575): Show |
chr5 | 10559070 | 10662816 |
| a0001c0003t0022 | 0/0 | 9580 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9575): Show |
chr5 | 10559070 | 10662816 |
| a0001c0003t0060 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0004t0002 | 0/0 | 9582 | 13 | 0 | 7 | 0 | 2 | 4 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0004t0014 | 0/0 | 9582 | 3 | 0 | 3 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0004t0039 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0004t0040 | 0/0 | 9582 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0005t0002 | 0/0 | 9582 | 11 | 0 | 6 | 3 | 0 | 2 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0005t0014 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0005t0023 | 0/0 | 9588 | 2 | 0 | 1 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0005t0063 | 0/0 | 9582 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0006t0003 | 0/0 | 9581 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0006t0007 | 0/0 | 9580 | 3 | 0 | 0 | 2 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9575): Show |
chr5 | 10559070 | 10662816 |
| a0001c0006t0058 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0007t0001 | 0/0 | 9586 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0007t0005 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0007t0024 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0009t0008 | 0/0 | 9588 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0009t0064 | 0/0 | 9588 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0011t0001 | 1/0 | 9586 | 2 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0011t0012 | 0/0 | 9584 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9579): Show |
chr5 | 10559070 | 10662816 |
| a0001c0013t0011 | 0/0 | 9582 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0014t0008 | 0/0 | 9588 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0015t0001 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0015t0004 | 0/0 | 9586 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0020t0044 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0021t0011 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0023t0001 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0024t0011 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0025t0019 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0026t0008 | 0/0 | 9588 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9583): Show |
chr5 | 10559070 | 10662816 |
| a0001c0030t0019 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0031t0062 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0001c0033t0038 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0001c0034t0001 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0001c0037t0002 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0002c0010t0015 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0002c0010t0018 | 0/0 | 9582 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0002c0010t0036 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0002c0012t0015 | 0/0 | 9582 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0002c0012t0034 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0002c0028t0037 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0003c0016t0001 | 0/0 | 9586 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0003c0019t0028 | 0/0 | 9586 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0003c0035t0001 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0004c0008t0010 | 0/0 | 9576 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9571): Show |
chr5 | 10559070 | 10662816 |
| a0005c0017t0020 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0005c0017t0021 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0005c0027t0021 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0006c0018t0035 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0006c0018t0061 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0007c0022t0020 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9577): Show |
chr5 | 10559070 | 10662816 |
| a0008c0036t0001 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9581): Show |
chr5 | 10559070 | 10662816 |
| a0009c0032t0003 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9576): Show |
chr5 | 10559070 | 10662816 |
| a0010c0029t0041 | 0/0 | 9580 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | AGTGA others(9575): Show |
chr5 | 10559070 | 10662816 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0009g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0009g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0012g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0013g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0013g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0013g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0024g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0025g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0025g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0026g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0026g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0027g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0029g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0029g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0031g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0031g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0032g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0032g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0033g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0042g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0045g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0047g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0048g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0049g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0051g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0052g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0054g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0055g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0056g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0057g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0059g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0065g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0066g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0067g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0001t0068g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0016g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0016g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0016g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0027g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0030g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0030g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0043g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0046g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0050g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0002t0053g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0007g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0007g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0017g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0017g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0017g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0022g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0022g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0003t0060g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0014g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0014g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0014g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0039g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0004t0040g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0014g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0023g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0023g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0005t0063g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0006t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0006t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0006t0007g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0006t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0006t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0006t0058g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0007t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0007t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0007t0024g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0009t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0009t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0009t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0009t0064g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0011t0001g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0011t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0013t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0013t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0013t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0014t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0014t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0014t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0015t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0015t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0015t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0020t0044g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0021t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0023t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0024t0011g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0025t0019g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0026t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0030t0019g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0031t0062g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0033t0038g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0034t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0001c0037t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0010t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0010t0018g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0010t0018g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0010t0036g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0012t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0012t0015g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0012t0034g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0002c0028t0037g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0003c0016t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0003c0016t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0003c0019t0028g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0003c0019t0028g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0003c0035t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0004c0008t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0004c0008t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0004c0008t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0004c0008t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0004c0008t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0005c0017t0020g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0005c0017t0021g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0005c0027t0021g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0006c0018t0035g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0006c0018t0061g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0007c0022t0020g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0008c0036t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0009c0032t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| a0010c0029t0041g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0147 | EUR | GBR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00140 | hp2 | a0001 | c0001 | t0066 | g0110 | EUR | GBR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | FIN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0189 | EUR | FIN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00408 | hp1 | a0001 | c0003 | t0003 | g0124 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0212 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00544 | hp2 | a0001 | c0007 | t0001 | g0194 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00558 | hp1 | a0001 | c0001 | t0056 | g0173 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00639 | hp2 | a0001 | c0006 | t0058 | g0023 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00642 | hp1 | a0001 | c0004 | t0014 | g0111 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00642 | hp2 | a0001 | c0004 | t0002 | g0143 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00673 | hp2 | a0001 | c0037 | t0002 | g0188 | EAS | CHS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00735 | hp1 | a0001 | c0005 | t0002 | g0208 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0046 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00738 | hp1 | a0001 | c0001 | t0067 | g0101 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG00741 | hp2 | a0001 | c0005 | t0023 | g0223 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01069 | hp1 | a0002 | c0028 | t0037 | g0007 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0141 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01070 | hp2 | a0001 | c0001 | t0025 | g0320 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01071 | hp1 | a0001 | c0001 | t0025 | g0319 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0262 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01074 | hp2 | a0001 | c0001 | t0029 | g0239 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01081 | hp1 | a0001 | c0005 | t0002 | g0135 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01081 | hp2 | a0001 | c0004 | t0014 | g0109 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01099 | hp2 | a0001 | c0002 | t0016 | g0049 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01106 | hp2 | a0001 | c0001 | t0049 | g0321 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01109 | hp2 | a0001 | c0001 | t0054 | g0033 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0197 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0139 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0196 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01169 | hp2 | a0001 | c0002 | t0016 | g0048 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01192 | hp1 | a0001 | c0002 | t0043 | g0221 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01192 | hp2 | a0001 | c0004 | t0002 | g0256 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0016 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01255 | hp1 | a0002 | c0012 | t0015 | g0285 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01255 | hp2 | a0001 | c0004 | t0039 | g0217 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01258 | hp1 | a0001 | c0005 | t0002 | g0067 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01258 | hp2 | a0001 | c0004 | t0014 | g0108 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01261 | hp2 | a0001 | c0033 | t0038 | g0044 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01358 | hp1 | a0001 | c0002 | t0027 | g0070 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01358 | hp2 | a0001 | c0005 | t0002 | g0174 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01361 | hp1 | a0001 | c0009 | t0008 | g0289 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01433 | hp1 | a0001 | c0005 | t0014 | g0086 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01433 | hp2 | a0001 | c0005 | t0002 | g0120 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01515 | hp1 | a0001 | c0005 | t0023 | g0233 | EUR | IBS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01516 | hp1 | a0001 | c0004 | t0002 | g0227 | EUR | IBS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0216 | EUR | IBS | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01884 | hp1 | a0001 | c0002 | t0053 | g0017 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01884 | hp2 | a0001 | c0009 | t0064 | g0085 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01952 | hp1 | a0001 | c0004 | t0002 | g0123 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01978 | hp1 | a0001 | c0004 | t0002 | g0042 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01978 | hp2 | a0001 | c0003 | t0003 | g0036 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0205 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0225 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0202 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02027 | hp1 | a0001 | c0007 | t0001 | g0160 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02055 | hp1 | a0001 | c0015 | t0001 | g0243 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02056 | hp2 | a0001 | c0005 | t0002 | g0253 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02083 | hp2 | a0001 | c0001 | t0048 | g0117 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02132 | hp1 | a0001 | c0006 | t0003 | g0132 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02132 | hp2 | a0001 | c0020 | t0044 | g0158 | EAS | KHV | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0201 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02148 | hp2 | a0001 | c0001 | t0013 | g0035 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02155 | hp1 | a0001 | c0006 | t0003 | g0267 | EAS | CDX | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02155 | hp2 | a0001 | c0007 | t0001 | g0192 | EAS | CDX | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02165 | hp1 | a0001 | c0003 | t0003 | g0145 | EAS | CDX | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02165 | hp2 | a0001 | c0002 | t0046 | g0177 | EAS | CDX | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02257 | hp2 | a0003 | c0035 | t0001 | g0122 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02258 | hp1 | a0005 | c0017 | t0021 | g0127 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02258 | hp2 | a0003 | c0016 | t0001 | g0010 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02273 | hp1 | a0001 | c0001 | t0013 | g0214 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0280 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02280 | hp1 | a0002 | c0010 | t0018 | g0306 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02293 | hp1 | a0001 | c0001 | t0055 | g0116 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02293 | hp2 | a0001 | c0001 | t0009 | g0316 | AMR | PEL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02451 | hp1 | a0001 | c0001 | t0059 | g0021 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02451 | hp2 | a0001 | c0015 | t0004 | g0104 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02572 | hp2 | a0003 | c0019 | t0028 | g0232 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02602 | hp1 | a0001 | c0001 | t0042 | g0198 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02615 | hp1 | a0001 | c0026 | t0008 | g0008 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02622 | hp1 | a0001 | c0011 | t0012 | g0003 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02622 | hp2 | a0001 | c0031 | t0062 | g0114 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02630 | hp1 | a0001 | c0013 | t0011 | g0014 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02630 | hp2 | a0001 | c0023 | t0001 | g0029 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02647 | hp1 | a0001 | c0014 | t0008 | g0018 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02683 | hp2 | a0001 | c0006 | t0007 | g0059 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02698 | hp1 | a0001 | c0003 | t0017 | g0080 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02723 | hp1 | a0001 | c0015 | t0004 | g0105 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02723 | hp2 | a0001 | c0013 | t0011 | g0030 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0034 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02735 | hp2 | a0001 | c0004 | t0002 | g0207 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0157 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02809 | hp2 | a0001 | c0001 | t0027 | g0133 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02818 | hp1 | a0001 | c0021 | t0011 | g0031 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02818 | hp2 | a0002 | c0010 | t0015 | g0026 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0236 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02886 | hp2 | a0003 | c0019 | t0028 | g0011 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02895 | hp2 | a0007 | c0022 | t0020 | g0005 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02896 | hp2 | a0004 | c0008 | t0010 | g0323 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02897 | hp2 | a0004 | c0008 | t0010 | g0324 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02922 | hp2 | a0001 | c0001 | t0032 | g0083 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02965 | hp1 | a0001 | c0011 | t0001 | g0001 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02965 | hp2 | a0006 | c0018 | t0061 | g0087 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02970 | hp1 | a0001 | c0009 | t0008 | g0313 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02970 | hp2 | a0001 | c0001 | t0029 | g0282 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02976 | hp1 | a0002 | c0012 | t0015 | g0020 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02976 | hp2 | a0001 | c0001 | t0033 | g0103 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0322 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03130 | hp1 | a0001 | c0009 | t0008 | g0304 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03139 | hp2 | a0006 | c0018 | t0035 | g0112 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03195 | hp1 | a0004 | c0008 | t0010 | g0074 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03209 | hp1 | a0001 | c0034 | t0001 | g0022 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03225 | hp2 | a0001 | c0014 | t0008 | g0128 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03239 | hp1 | a0001 | c0005 | t0002 | g0061 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03453 | hp1 | a0001 | c0001 | t0052 | g0025 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03453 | hp2 | a0005 | c0017 | t0020 | g0136 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03486 | hp1 | a0001 | c0014 | t0008 | g0125 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03486 | hp2 | a0001 | c0002 | t0050 | g0078 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03490 | hp1 | a0001 | c0002 | t0030 | g0037 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0312 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03491 | hp1 | a0001 | c0004 | t0002 | g0058 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03492 | hp1 | a0001 | c0002 | t0030 | g0039 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03516 | hp1 | a0001 | c0001 | t0047 | g0287 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0297 | AFR | ESN | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03540 | hp1 | a0002 | c0010 | t0018 | g0307 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03540 | hp2 | a0001 | c0025 | t0019 | g0002 | AFR | GWD | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03579 | hp1 | a0001 | c0024 | t0011 | g0028 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03579 | hp2 | a0001 | c0001 | t0033 | g0106 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03654 | hp1 | a0001 | c0005 | t0002 | g0299 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03688 | hp1 | a0001 | c0004 | t0040 | g0266 | SAS | STU | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03688 | hp2 | a0001 | c0005 | t0063 | g0089 | SAS | STU | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03831 | hp1 | a0001 | c0001 | t0068 | g0204 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03834 | hp1 | a0001 | c0004 | t0002 | g0293 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03834 | hp2 | a0001 | c0004 | t0002 | g0298 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03927 | hp2 | a0001 | c0003 | t0007 | g0309 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0081 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0294 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | BEB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG04228 | hp2 | a0001 | c0003 | t0007 | g0213 | SAS | STU | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | CHB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18747 | hp1 | a0001 | c0001 | t0057 | g0038 | EAS | CHB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | CHB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0288 | AFR | YRI | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18906 | hp2 | a0001 | c0013 | t0011 | g0279 | AFR | YRI | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18941 | hp1 | a0001 | c0003 | t0003 | g0186 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18941 | hp2 | a0001 | c0005 | t0002 | g0272 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18944 | hp2 | a0001 | c0003 | t0003 | g0153 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18946 | hp2 | a0001 | c0001 | t0065 | g0102 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0161 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18950 | hp1 | a0008 | c0036 | t0001 | g0047 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18952 | hp2 | a0001 | c0003 | t0003 | g0170 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18959 | hp2 | a0001 | c0003 | t0017 | g0091 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18960 | hp1 | a0001 | c0003 | t0003 | g0231 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18964 | hp1 | a0001 | c0007 | t0005 | g0179 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18964 | hp2 | a0001 | c0002 | t0004 | g0100 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18966 | hp2 | a0001 | c0006 | t0007 | g0269 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18967 | hp1 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18969 | hp1 | a0001 | c0006 | t0007 | g0191 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18969 | hp2 | a0001 | c0001 | t0031 | g0082 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18973 | hp1 | a0001 | c0003 | t0007 | g0259 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18973 | hp2 | a0001 | c0002 | t0004 | g0098 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18975 | hp1 | a0001 | c0007 | t0024 | g0155 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18975 | hp2 | a0001 | c0003 | t0022 | g0119 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18977 | hp1 | a0001 | c0003 | t0007 | g0215 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18983 | hp2 | a0001 | c0001 | t0024 | g0206 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18985 | hp1 | a0001 | c0003 | t0003 | g0053 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18986 | hp2 | a0001 | c0003 | t0017 | g0095 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18990 | hp1 | a0001 | c0001 | t0026 | g0210 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19009 | hp1 | a0001 | c0001 | t0026 | g0167 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19010 | hp1 | a0001 | c0007 | t0001 | g0154 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19010 | hp2 | a0009 | c0032 | t0003 | g0270 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19011 | hp1 | a0001 | c0001 | t0009 | g0260 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19012 | hp1 | a0001 | c0003 | t0007 | g0254 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19030 | hp1 | a0010 | c0029 | t0041 | g0146 | AFR | LWK | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19030 | hp2 | a0001 | c0030 | t0019 | g0199 | AFR | LWK | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | LWK | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19058 | hp2 | a0001 | c0002 | t0004 | g0099 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19060 | hp1 | a0001 | c0002 | t0004 | g0096 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19063 | hp2 | a0001 | c0003 | t0022 | g0041 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19064 | hp1 | a0001 | c0001 | t0045 | g0051 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19084 | hp2 | a0001 | c0001 | t0031 | g0317 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19087 | hp1 | a0001 | c0001 | t0051 | g0315 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19087 | hp2 | a0001 | c0003 | t0060 | g0093 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19088 | hp1 | a0001 | c0003 | t0007 | g0276 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19090 | hp1 | a0001 | c0005 | t0002 | g0055 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0107 | AFR | YRI | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA19240 | hp2 | a0001 | c0001 | t0032 | g0084 | AFR | YRI | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | TSI | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA20752 | hp2 | a0001 | c0004 | t0002 | g0144 | EUR | TSI | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | GIH | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0134 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG01123 | hp2 | a0001 | c0002 | t0016 | g0150 | AMR | CLM | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02109 | hp1 | a0002 | c0010 | t0036 | g0079 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02486 | hp1 | a0004 | c0008 | t0010 | g0292 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0284 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02559 | hp1 | a0002 | c0012 | t0034 | g0071 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03471 | hp1 | a0004 | c0008 | t0010 | g0075 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG03471 | hp2 | a0003 | c0016 | t0001 | g0006 | AFR | MSL | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | USA | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| HG06807 | hp2 | a0005 | c0027 | t0021 | g0004 | AFR | USA | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | USA | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | USA | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0152 | REF | REF | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| homoSapiens | grch38p0 | a0001 | c0011 | t0001 | g0009 | REF | REF | ANKRD33B_chr5_10559070_10662816 | ANKRD33B | chr5 | 10559070 | 10662816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:10618460 | C | T | 1 | a0008 | 1 | NA18950.hp1 | missense_variant&splice_region_variant | MODERATE | c.494C>T | p.Ala165Val | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/4 | 892/9586 | 494/1485 | 165/494 | chr5 | 10618460 | |||
| chr5:10638036 | A | G | 1 | a0003 | 5 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.505A>G | p.Ile169Val | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/4 | 903/9586 | 505/1485 | 169/494 | chr5 | 10638036 | |||
| chr5:10649370 | G | A | 1 | a0009 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.742G>A | p.Glu248Lys | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1140/9586 | 742/1485 | 248/494 | chr5 | 10649370 | |||
| chr5:10649433 | G | A | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.805G>A | p.Ala269Thr | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1203/9586 | 805/1485 | 269/494 | chr5 | 10649433 | |||
| chr5:10649703 | G | A | 1 | a0006 | 2 | HG02965.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.1075G>A | p.Glu359Lys | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1473/9586 | 1075/1485 | 359/494 | chr5 | 10649703 | |||
| chr5:10649729 | G | T | 1 | a0004 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.1101G>T | p.Gln367His | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1499/9586 | 1101/1485 | 367/494 | chr5 | 10649729 | |||
| chr5:10649730 | C | T | 1 | a0004 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.1102C>T | p.Arg368Cys | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1500/9586 | 1102/1485 | 368/494 | chr5 | 10649730 | |||
| chr5:10649742 | G | A | 2 | a0005 a0007 |
4 | HG02258.hp1 HG02895.hp2 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1114G>A | p.Gly372Arg | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1512/9586 | 1114/1485 | 372/494 | chr5 | 10649742 | |||
| chr5:10649796 | G | T | 1 | a0007 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.1168G>T | p.Ala390Ser | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1566/9586 | 1168/1485 | 390/494 | chr5 | 10649796 | |||
| chr5:10649797 | C | T | 1 | a0007 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.1169C>T | p.Ala390Val | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1567/9586 | 1169/1485 | 390/494 | chr5 | 10649797 | |||
| chr5:10649821 | C | T | 1 | a0002 | 8 | HG01069.hp1 HG01255.hp1 HG02109.hp1 others(5): Show |
missense_variant | MODERATE | c.1193C>T | p.Ala398Val | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1591/9586 | 1193/1485 | 398/494 | chr5 | 10649821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:10564659 | G | A | 1 | a0001c0020 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.192G>A | p.Glu64Glu | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/4 | 590/9586 | 192/1485 | 64/494 | chr5 | 10564659 | |||
| chr5:10564734 | C | T | 27 | a0001c0001 a0001c0002 a0001c0003 others(24): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
synonymous_variant | LOW | c.267C>T | p.Leu89Leu | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/4 | 665/9586 | 267/1485 | 89/494 | chr5 | 10564734 | |||
| chr5:10564758 | C | T | 2 | a0001c0007 a0001c0037 |
7 | HG00544.hp2 HG00673.hp2 HG02027.hp1 others(4): Show |
synonymous_variant | LOW | c.291C>T | p.Asn97Asn | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/4 | 689/9586 | 291/1485 | 97/494 | chr5 | 10564758 | |||
| chr5:10638068 | T | C | 16 | a0001c0002 a0001c0003 a0001c0005 others(13): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
synonymous_variant | LOW | c.537T>C | p.Pro179Pro | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/4 | 935/9586 | 537/1485 | 179/494 | chr5 | 10638068 | |||
| chr5:10649300 | G | C | 10 | a0001c0003 a0001c0006 a0001c0013 others(7): Show |
43 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(40): Show |
synonymous_variant | LOW | c.672G>C | p.Gly224Gly | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1070/9586 | 672/1485 | 224/494 | chr5 | 10649300 | |||
| chr5:10649489 | G | C | 3 | a0001c0009 a0001c0014 a0001c0026 |
8 | HG01361.hp1 HG01884.hp2 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.861G>C | p.Val287Val | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1259/9586 | 861/1485 | 287/494 | chr5 | 10649489 | |||
| chr5:10649513 | C | T | 3 | a0001c0025 a0001c0030 a0001c0033 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.885C>T | p.Ser295Ser | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1283/9586 | 885/1485 | 295/494 | chr5 | 10649513 | |||
| chr5:10649573 | C | T | 1 | a0001c0015 | 3 | HG02055.hp1 HG02451.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.945C>T | p.Leu315Leu | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1343/9586 | 945/1485 | 315/494 | chr5 | 10649573 | |||
| chr5:10649672 | G | A | 20 | a0001c0003 a0001c0004 a0001c0005 others(17): Show |
94 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(91): Show |
synonymous_variant | LOW | c.1044G>A | p.Ala348Ala | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1442/9586 | 1044/1485 | 348/494 | chr5 | 10649672 | |||
| chr5:10649894 | G | A | 1 | a0001c0034 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1266G>A | p.Val422Val | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1664/9586 | 1266/1485 | 422/494 | chr5 | 10649894 | |||
| chr5:10649930 | C | G | 3 | a0001c0013 a0001c0021 a0001c0024 |
5 | HG02630.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.1302C>G | p.Pro434Pro | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1700/9586 | 1302/1485 | 434/494 | chr5 | 10649930 | |||
| chr5:10649978 | C | T | 1 | a0001c0031 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1350C>T | p.Ser450Ser | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1748/9586 | 1350/1485 | 450/494 | chr5 | 10649978 | |||
| chr5:10650038 | A | G | 25 | a0001c0003 a0001c0004 a0001c0005 others(22): Show |
105 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(102): Show |
synonymous_variant | LOW | c.1410A>G | p.Ala470Ala | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1808/9586 | 1410/1485 | 470/494 | chr5 | 10650038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:10564143 | C | T | 18 | a0001c0001t0004 a0001c0001t0031 a0001c0001t0032 others(15): Show |
35 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-325C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/4 | 325 | chr5 | 10564143 | ||||||
| chr5:10564162 | C | T | 1 | a0001c0001t0068 | 1 | HG03831.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-306C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/4 | chr5 | 10564162 | |||||||
| chr5:10564206 | C | G | 2 | a0001c0001t0059 a0001c0006t0058 |
2 | HG00639.hp2 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-262C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/4 | 262 | chr5 | 10564206 | ||||||
| chr5:10650130 | C | CGCTGGGG others(5): Show |
1 | a0001c0001t0068 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32_*43dupTGGGGCCG others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 44 | INFO_REALIGN_3_PRIME | chr5 | 10650130 | |||||
| chr5:10650139 | CGGGGCT | C | 38 | a0001c0003t0003 a0001c0003t0007 a0001c0003t0017 others(35): Show |
95 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*32_*37delTGGGGC | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 32 | INFO_REALIGN_3_PRIME | chr5 | 10650139 | |||||
| chr5:10650145 | T | C | 1 | a0001c0005t0023 | 2 | HG00741.hp2 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*32T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 32 | chr5 | 10650145 | ||||||
| chr5:10650195 | G | A | 1 | a0002c0012t0034 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 82 | chr5 | 10650195 | ||||||
| chr5:10650212 | T | G | 43 | a0001c0003t0003 a0001c0003t0007 a0001c0003t0017 others(40): Show |
105 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*99T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 99 | chr5 | 10650212 | ||||||
| chr5:10650213 | T | G | 43 | a0001c0003t0003 a0001c0003t0007 a0001c0003t0017 others(40): Show |
105 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*100T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 100 | chr5 | 10650213 | ||||||
| chr5:10650280 | G | A | 4 | a0001c0003t0003 a0001c0003t0060 a0001c0006t0003 others(1): Show |
19 | HG00408.hp1 HG00544.hp1 HG01074.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*167G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 167 | chr5 | 10650280 | ||||||
| chr5:10650297 | G | A | 1 | a0001c0001t0042 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 184 | chr5 | 10650297 | ||||||
| chr5:10650478 | T | C | 2 | a0006c0018t0035 a0006c0018t0061 |
2 | HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*365T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 365 | chr5 | 10650478 | ||||||
| chr5:10650596 | G | A | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*483G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 483 | chr5 | 10650596 | ||||||
| chr5:10650619 | G | T | 6 | a0001c0003t0007 a0001c0003t0017 a0001c0003t0022 others(3): Show |
16 | HG00639.hp2 HG02683.hp2 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*506G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 506 | chr5 | 10650619 | ||||||
| chr5:10650620 | G | T | 6 | a0001c0003t0007 a0001c0003t0017 a0001c0003t0022 others(3): Show |
16 | HG00639.hp2 HG02683.hp2 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 507 | chr5 | 10650620 | ||||||
| chr5:10650682 | T | A | 39 | a0001c0003t0003 a0001c0003t0007 a0001c0003t0017 others(36): Show |
97 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*569T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 569 | chr5 | 10650682 | ||||||
| chr5:10650731 | A | G | 4 | a0005c0017t0020 a0005c0017t0021 a0005c0027t0021 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*618A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 618 | chr5 | 10650731 | ||||||
| chr5:10650981 | T | A | 1 | a0001c0031t0062 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 868 | chr5 | 10650981 | ||||||
| chr5:10651144 | G | A | 1 | a0001c0003t0022 | 2 | NA18975.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1031 | chr5 | 10651144 | ||||||
| chr5:10651287 | C | T | 1 | a0001c0001t0057 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1174C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1174 | chr5 | 10651287 | ||||||
| chr5:10651317 | C | A | 3 | a0002c0010t0018 a0002c0010t0036 a0002c0028t0037 |
4 | HG01069.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1204C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1204 | chr5 | 10651317 | ||||||
| chr5:10651594 | T | C | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1481T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1481 | chr5 | 10651594 | ||||||
| chr5:10651676 | T | C | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1563T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1563 | chr5 | 10651676 | ||||||
| chr5:10651746 | G | C | 2 | a0006c0018t0035 a0006c0018t0061 |
2 | HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1633G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1633 | chr5 | 10651746 | ||||||
| chr5:10651874 | T | A | 40 | a0001c0002t0043 a0001c0003t0003 a0001c0003t0007 others(37): Show |
98 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1761T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1761 | chr5 | 10651874 | ||||||
| chr5:10651929 | G | A | 39 | a0001c0002t0043 a0001c0003t0003 a0001c0003t0007 others(36): Show |
97 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1816G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1816 | chr5 | 10651929 | ||||||
| chr5:10651982 | A | G | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1869A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1869 | chr5 | 10651982 | ||||||
| chr5:10652005 | C | T | 40 | a0001c0002t0043 a0001c0003t0003 a0001c0003t0007 others(37): Show |
98 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1892C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1892 | chr5 | 10652005 | ||||||
| chr5:10652077 | T | TG | 3 | a0001c0013t0011 a0001c0021t0011 a0001c0024t0011 |
5 | HG02630.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1968dupG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 1969 | INFO_REALIGN_3_PRIME | chr5 | 10652077 | |||||
| chr5:10652117 | C | T | 2 | a0002c0010t0015 a0002c0012t0015 |
3 | HG01255.hp1 HG02818.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2004 | chr5 | 10652117 | ||||||
| chr5:10652129 | AG | A | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2017delG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2017 | chr5 | 10652129 | ||||||
| chr5:10652174 | C | G | 2 | a0001c0001t0009 a0001c0001t0067 |
7 | HG00738.hp1 HG01123.hp1 HG02004.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2061C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2061 | chr5 | 10652174 | ||||||
| chr5:10652191 | C | A | 1 | a0001c0002t0043 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2078C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2078 | chr5 | 10652191 | ||||||
| chr5:10652201 | A | G | 40 | a0001c0002t0043 a0001c0003t0003 a0001c0003t0007 others(37): Show |
98 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*2088A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2088 | chr5 | 10652201 | ||||||
| chr5:10652281 | G | T | 1 | a0001c0002t0030 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2168G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2168 | chr5 | 10652281 | ||||||
| chr5:10652310 | G | A | 3 | a0001c0025t0019 a0001c0030t0019 a0001c0033t0038 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2197G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2197 | chr5 | 10652310 | ||||||
| chr5:10652323 | C | T | 1 | a0001c0001t0029 | 2 | HG01074.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2210C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2210 | chr5 | 10652323 | ||||||
| chr5:10652332 | G | A | 3 | a0001c0025t0019 a0001c0030t0019 a0001c0033t0038 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2219G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2219 | chr5 | 10652332 | ||||||
| chr5:10652344 | G | A | 4 | a0001c0003t0003 a0001c0003t0060 a0001c0006t0003 others(1): Show |
19 | HG00408.hp1 HG00544.hp1 HG01074.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2231G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2231 | chr5 | 10652344 | ||||||
| chr5:10652354 | C | G | 1 | a0001c0004t0039 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2241C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2241 | chr5 | 10652354 | ||||||
| chr5:10652496 | A | AAG | 5 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0065 others(2): Show |
16 | HG00609.hp2 HG02071.hp2 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2383_*2384insAG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2384 | chr5 | 10652496 | ||||||
| chr5:10652498 | A | T | 5 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0065 others(2): Show |
16 | HG00609.hp2 HG02071.hp2 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2385A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2385 | chr5 | 10652498 | ||||||
| chr5:10652500 | A | G | 1 | a0001c0001t0042 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2387A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2387 | chr5 | 10652500 | ||||||
| chr5:10652500 | ATTCCTG | A | 5 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0065 others(2): Show |
16 | HG00609.hp2 HG02071.hp2 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2388_*2393delTTCC others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2388 | chr5 | 10652500 | ||||||
| chr5:10652734 | C | T | 1 | a0002c0028t0037 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2621C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2621 | chr5 | 10652734 | ||||||
| chr5:10652742 | G | T | 1 | a0010c0029t0041 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2629G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2629 | chr5 | 10652742 | ||||||
| chr5:10652743 | G | T | 1 | a0010c0029t0041 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2630G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2630 | chr5 | 10652743 | ||||||
| chr5:10652901 | G | A | 2 | a0006c0018t0035 a0006c0018t0061 |
2 | HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2788G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2788 | chr5 | 10652901 | ||||||
| chr5:10652987 | G | C | 5 | a0002c0010t0015 a0002c0010t0018 a0002c0010t0036 others(2): Show |
7 | HG01069.hp1 HG01255.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2874G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2874 | chr5 | 10652987 | ||||||
| chr5:10653038 | T | G | 3 | a0001c0013t0011 a0001c0021t0011 a0001c0024t0011 |
5 | HG02630.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2925T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 2925 | chr5 | 10653038 | ||||||
| chr5:10653392 | T | A | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3279T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3279 | chr5 | 10653392 | ||||||
| chr5:10653677 | C | T | 2 | a0006c0018t0035 a0006c0018t0061 |
2 | HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3564C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3564 | chr5 | 10653677 | ||||||
| chr5:10653681 | C | G | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3568C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3568 | chr5 | 10653681 | ||||||
| chr5:10653731 | C | G | 1 | a0001c0001t0056 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3618C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3618 | chr5 | 10653731 | ||||||
| chr5:10653742 | C | A | 2 | a0001c0001t0024 a0001c0007t0024 |
2 | NA18975.hp1 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3629C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3629 | chr5 | 10653742 | ||||||
| chr5:10653769 | A | G | 1 | a0001c0001t0055 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3656A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3656 | chr5 | 10653769 | ||||||
| chr5:10653934 | G | A | 2 | a0006c0018t0035 a0006c0018t0061 |
2 | HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3821G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3821 | chr5 | 10653934 | ||||||
| chr5:10653988 | C | T | 12 | a0001c0002t0043 a0001c0004t0002 a0001c0004t0014 others(9): Show |
37 | HG00642.hp1 HG00642.hp2 HG00673.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3875C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 3875 | chr5 | 10653988 | ||||||
| chr5:10654129 | C | A | 14 | a0001c0002t0043 a0001c0004t0002 a0001c0004t0014 others(11): Show |
39 | HG00642.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4016C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4016 | chr5 | 10654129 | ||||||
| chr5:10654206 | G | A | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4093G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4093 | chr5 | 10654206 | ||||||
| chr5:10654231 | C | T | 1 | a0001c0001t0054 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4118C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4118 | chr5 | 10654231 | ||||||
| chr5:10654512 | A | G | 1 | a0001c0020t0044 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4399A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4399 | chr5 | 10654512 | ||||||
| chr5:10654619 | A | G | 1 | a0001c0002t0053 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4506A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4506 | chr5 | 10654619 | ||||||
| chr5:10654657 | C | G | 44 | a0001c0001t0052 a0001c0002t0043 a0001c0003t0003 others(41): Show |
106 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*4544C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4544 | chr5 | 10654657 | ||||||
| chr5:10654667 | C | G | 3 | a0001c0025t0019 a0001c0030t0019 a0001c0033t0038 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4554C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4554 | chr5 | 10654667 | ||||||
| chr5:10654755 | C | T | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4642C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4642 | chr5 | 10654755 | ||||||
| chr5:10654775 | C | G | 3 | a0001c0031t0062 a0006c0018t0035 a0006c0018t0061 |
3 | HG02622.hp2 HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4662C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4662 | chr5 | 10654775 | ||||||
| chr5:10654829 | A | G | 1 | a0001c0001t0051 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4716A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4716 | chr5 | 10654829 | ||||||
| chr5:10654889 | C | T | 6 | a0001c0003t0007 a0001c0003t0017 a0001c0003t0022 others(3): Show |
16 | HG00639.hp2 HG02683.hp2 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4776C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4776 | chr5 | 10654889 | ||||||
| chr5:10655095 | A | C | 1 | a0001c0031t0062 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4982A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 4982 | chr5 | 10655095 | ||||||
| chr5:10655173 | G | A | 1 | a0001c0033t0038 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5060G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5060 | chr5 | 10655173 | ||||||
| chr5:10655203 | G | A | 1 | a0001c0001t0025 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5090G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5090 | chr5 | 10655203 | ||||||
| chr5:10655424 | A | G | 1 | a0001c0002t0050 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5311A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5311 | chr5 | 10655424 | ||||||
| chr5:10655483 | A | T | 1 | a0001c0006t0058 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5370A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5370 | chr5 | 10655483 | ||||||
| chr5:10655509 | G | A | 1 | a0001c0001t0045 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5396G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5396 | chr5 | 10655509 | ||||||
| chr5:10655600 | C | T | 1 | a0001c0001t0066 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5487C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5487 | chr5 | 10655600 | ||||||
| chr5:10655614 | G | A | 1 | a0001c0006t0058 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5501G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5501 | chr5 | 10655614 | ||||||
| chr5:10655730 | C | T | 46 | a0001c0001t0052 a0001c0002t0043 a0001c0003t0003 others(43): Show |
109 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*5617C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5617 | chr5 | 10655730 | ||||||
| chr5:10655866 | G | A | 3 | a0001c0001t0051 a0002c0010t0036 a0002c0028t0037 |
3 | HG01069.hp1 HG02109.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5753G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5753 | chr5 | 10655866 | ||||||
| chr5:10655875 | C | T | 6 | a0001c0003t0007 a0001c0003t0017 a0001c0003t0022 others(3): Show |
16 | HG00639.hp2 HG02683.hp2 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5762C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5762 | chr5 | 10655875 | ||||||
| chr5:10655885 | A | G | 46 | a0001c0001t0052 a0001c0002t0043 a0001c0003t0003 others(43): Show |
109 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*5772A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5772 | chr5 | 10655885 | ||||||
| chr5:10655909 | T | C | 2 | a0003c0019t0028 a0004c0008t0010 |
7 | HG02486.hp1 HG02572.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5796T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5796 | chr5 | 10655909 | ||||||
| chr5:10656050 | C | T | 46 | a0001c0001t0052 a0001c0002t0043 a0001c0003t0003 others(43): Show |
109 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*5937C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5937 | chr5 | 10656050 | ||||||
| chr5:10656074 | C | T | 44 | a0001c0001t0052 a0001c0002t0043 a0001c0003t0003 others(41): Show |
102 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5961C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 5961 | chr5 | 10656074 | ||||||
| chr5:10656158 | C | T | 3 | a0001c0013t0011 a0001c0021t0011 a0001c0024t0011 |
5 | HG02630.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6045C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6045 | chr5 | 10656158 | ||||||
| chr5:10656586 | T | C | 45 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(42): Show |
109 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*6473T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6473 | chr5 | 10656586 | ||||||
| chr5:10656647 | C | T | 1 | a0001c0001t0065 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6534C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6534 | chr5 | 10656647 | ||||||
| chr5:10656662 | T | C | 1 | a0001c0002t0046 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6549T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6549 | chr5 | 10656662 | ||||||
| chr5:10656673 | G | A | 43 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(40): Show |
102 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*6560G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6560 | chr5 | 10656673 | ||||||
| chr5:10656765 | C | T | 4 | a0001c0001t0006 a0001c0001t0033 a0001c0001t0049 others(1): Show |
15 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6652C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6652 | chr5 | 10656765 | ||||||
| chr5:10656887 | G | A | 1 | a0001c0002t0016 | 3 | HG01099.hp2 HG01123.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6774G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6774 | chr5 | 10656887 | ||||||
| chr5:10656979 | G | GA | 13 | a0001c0001t0047 a0001c0003t0003 a0001c0003t0060 others(10): Show |
30 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6877dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6878 | INFO_REALIGN_3_PRIME | chr5 | 10656979 | |||||
| chr5:10656979 | G | GAA | 28 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(25): Show |
60 | HG00642.hp1 HG00642.hp2 HG00673.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*6876_*6877dupAA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6878 | INFO_REALIGN_3_PRIME | chr5 | 10656979 | |||||
| chr5:10656991 | C | A | 4 | a0001c0001t0013 a0001c0013t0011 a0001c0021t0011 others(1): Show |
9 | HG01167.hp1 HG01169.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6878C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6878 | chr5 | 10656991 | ||||||
| chr5:10657002 | T | A | 3 | a0001c0025t0019 a0001c0030t0019 a0001c0033t0038 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6889T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6889 | chr5 | 10657002 | ||||||
| chr5:10657003 | T | C | 3 | a0001c0025t0019 a0001c0030t0019 a0001c0033t0038 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6890T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6890 | chr5 | 10657003 | ||||||
| chr5:10657022 | C | T | 47 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(44): Show |
111 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*6909C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6909 | chr5 | 10657022 | ||||||
| chr5:10657078 | A | G | 1 | a0001c0001t0048 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6965A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6965 | chr5 | 10657078 | ||||||
| chr5:10657082 | G | A | 47 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(44): Show |
111 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*6969G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6969 | chr5 | 10657082 | ||||||
| chr5:10657097 | T | C | 45 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(42): Show |
109 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*6984T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6984 | chr5 | 10657097 | ||||||
| chr5:10657104 | A | G | 3 | a0001c0031t0062 a0006c0018t0035 a0006c0018t0061 |
3 | HG02622.hp2 HG02965.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6991A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 6991 | chr5 | 10657104 | ||||||
| chr5:10657158 | G | A | 3 | a0001c0001t0027 a0001c0001t0032 a0001c0002t0027 |
4 | HG01358.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7045G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 7045 | chr5 | 10657158 | ||||||
| chr5:10657181 | C | T | 47 | a0001c0001t0026 a0001c0001t0052 a0001c0002t0043 others(44): Show |
111 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*7068C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 7068 | chr5 | 10657181 | ||||||
| chr5:10657333 | A | T | 2 | a0005c0017t0020 a0007c0022t0020 |
2 | HG02895.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7220A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 7220 | chr5 | 10657333 | ||||||
| chr5:10657490 | A | G | 1 | a0001c0001t0049 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7377A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 7377 | chr5 | 10657490 | ||||||
| chr5:10657500 | CTG | C | 4 | a0001c0001t0012 a0001c0001t0059 a0001c0002t0053 others(1): Show |
7 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7391_*7392delGT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 7391 | INFO_REALIGN_3_PRIME | chr5 | 10657500 | |||||
| chr5:10657646 | TTAA | T | 1 | a0004c0008t0010 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7538_*7540delAAT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 4/4 | 7538 | INFO_REALIGN_3_PRIME | chr5 | 10657646 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:10564915 | C | G | 313 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(310): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.366+82C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10564915 | |||||||
| chr5:10565111 | G | C | 16 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0015 others(13): Show |
16 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.366+278G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565111 | |||||||
| chr5:10565117 | C | T | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+284C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565117 | |||||||
| chr5:10565133 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.366+300G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565133 | |||||||
| chr5:10565139 | G | T | 209 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0126 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.366+306G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565139 | |||||||
| chr5:10565140 | C | T | 4 | a0001c0001t0049g0321 a0001c0002t0006g0322 a0004c0008t0010g0323 others(1): Show |
4 | HG01106.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+307C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565140 | |||||||
| chr5:10565160 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+327A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565160 | |||||||
| chr5:10565175 | C | T | 1 | a0001c0031t0062g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.366+342C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565175 | |||||||
| chr5:10565189 | C | T | 2 | a0001c0001t0025g0319 a0001c0001t0025g0320 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.366+356C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565189 | |||||||
| chr5:10565246 | G | A | 1 | a0001c0001t0055g0116 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.366+413G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565246 | |||||||
| chr5:10565488 | A | G | 2 | a0001c0001t0006g0113 a0006c0018t0035g0112 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+655A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565488 | |||||||
| chr5:10565518 | A | C | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+685A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565518 | |||||||
| chr5:10565655 | A | G | 1 | a0001c0002t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.366+822A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565655 | |||||||
| chr5:10565765 | C | T | 34 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0004g0090 others(31): Show |
34 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.366+932C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565765 | |||||||
| chr5:10565864 | A | T | 220 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0121 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.366+1031A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565864 | |||||||
| chr5:10565906 | C | G | 1 | a0001c0001t0009g0316 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.366+1073C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565906 | |||||||
| chr5:10565969 | G | A | 1 | a0001c0001t0048g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.366+1136G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10565969 | |||||||
| chr5:10566062 | A | G | 16 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0015 others(13): Show |
16 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.366+1229A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566062 | |||||||
| chr5:10566089 | A | G | 38 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0060 others(35): Show |
38 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.366+1256A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566089 | |||||||
| chr5:10566092 | C | T | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.366+1259C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566092 | |||||||
| chr5:10566209 | G | A | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+1376G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566209 | |||||||
| chr5:10566439 | G | C | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+1606G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566439 | |||||||
| chr5:10566442 | C | T | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+1609C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566442 | |||||||
| chr5:10566566 | G | A | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+1733G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566566 | |||||||
| chr5:10566793 | T | C | 2 | a0001c0023t0001g0029 a0001c0024t0011g0028 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.366+1960T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566793 | |||||||
| chr5:10566836 | G | A | 1 | a0001c0001t0005g0118 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.366+2003G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566836 | |||||||
| chr5:10566891 | A | C | 1 | a0001c0001t0051g0315 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.366+2058A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566891 | |||||||
| chr5:10566909 | G | T | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+2076G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566909 | |||||||
| chr5:10566923 | T | C | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+2090T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10566923 | |||||||
| chr5:10567015 | G | A | 1 | a0001c0003t0022g0119 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.366+2182G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567015 | |||||||
| chr5:10567186 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.366+2353G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567186 | |||||||
| chr5:10567367 | G | T | 16 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0015 others(13): Show |
16 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.366+2534G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567367 | |||||||
| chr5:10567378 | T | C | 1 | a0001c0005t0002g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.366+2545T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567378 | |||||||
| chr5:10567399 | T | C | 314 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.366+2566T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567399 | |||||||
| chr5:10567431 | T | G | 17 | a0001c0001t0001g0121 a0001c0001t0006g0012 a0001c0001t0006g0013 others(14): Show |
17 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.366+2598T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567431 | |||||||
| chr5:10567520 | G | A | 1 | a0003c0019t0028g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.366+2687G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567520 | |||||||
| chr5:10567625 | A | G | 293 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.366+2792A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567625 | |||||||
| chr5:10567665 | A | G | 3 | a0001c0023t0001g0029 a0001c0024t0011g0028 a0003c0016t0001g0010 |
3 | HG02258.hp2 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.366+2832A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567665 | |||||||
| chr5:10567673 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+2840C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567673 | |||||||
| chr5:10567693 | G | A | 1 | a0003c0035t0001g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.366+2860G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567693 | |||||||
| chr5:10567866 | G | A | 16 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0015 others(13): Show |
16 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.366+3033G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567866 | |||||||
| chr5:10567923 | C | T | 16 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0015 others(13): Show |
16 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.366+3090C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10567923 | |||||||
| chr5:10568214 | T | C | 2 | a0001c0001t0004g0081 a0001c0003t0017g0080 |
2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.366+3381T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568214 | |||||||
| chr5:10568305 | A | G | 223 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0076 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.366+3472A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568305 | |||||||
| chr5:10568450 | C | A | 1 | a0001c0004t0002g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.366+3617C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568450 | |||||||
| chr5:10568479 | A | G | 34 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0004g0090 others(31): Show |
34 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.366+3646A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568479 | |||||||
| chr5:10568595 | C | T | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0002t0001g0063 others(4): Show |
7 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+3762C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568595 | |||||||
| chr5:10568620 | C | A | 4 | a0001c0001t0006g0113 a0001c0002t0027g0070 a0002c0012t0034g0071 others(1): Show |
4 | HG01358.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+3787C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568620 | |||||||
| chr5:10568679 | C | T | 1 | a0001c0009t0008g0313 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.366+3846C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568679 | |||||||
| chr5:10568809 | C | T | 4 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0002t0001g0312 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+3976C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568809 | |||||||
| chr5:10568880 | A | G | 35 | a0001c0001t0001g0115 a0001c0001t0004g0081 a0001c0001t0004g0088 others(32): Show |
35 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.366+4047A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568880 | |||||||
| chr5:10568961 | G | C | 34 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0004g0090 others(31): Show |
34 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.366+4128G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10568961 | |||||||
| chr5:10569012 | C | T | 2 | a0001c0001t0006g0113 a0006c0018t0035g0112 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+4179C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569012 | |||||||
| chr5:10569068 | C | A | 268 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0121 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.366+4235C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569068 | |||||||
| chr5:10569136 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.366+4303C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569136 | |||||||
| chr5:10569146 | A | G | 277 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0076 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.366+4313A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569146 | |||||||
| chr5:10569368 | A | G | 39 | a0001c0001t0001g0301 a0001c0001t0004g0081 a0001c0001t0004g0088 others(36): Show |
39 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.366+4535A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569368 | |||||||
| chr5:10569458 | T | C | 1 | a0001c0003t0003g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.366+4625T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569458 | |||||||
| chr5:10569597 | A | AAAAT | 195 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0156 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.366+4790_366+4793d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10569597 | ||||||
| chr5:10569597 | A | AAAATAAA others(1): Show |
28 | a0001c0001t0001g0076 a0001c0001t0001g0115 a0001c0001t0001g0130 others(25): Show |
28 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.366+4786_366+4793d others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10569597 | ||||||
| chr5:10569597 | A | AAAATAAA others(5): Show |
12 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0006g0113 others(9): Show |
12 | HG02258.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.366+4782_366+4793d others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10569597 | ||||||
| chr5:10569597 | A | AAAATAAA others(9): Show |
25 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0004g0090 others(22): Show |
25 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.366+4778_366+4793d others(18): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10569597 | ||||||
| chr5:10569597 | A | AAAATAAA others(13): Show |
5 | a0001c0001t0032g0083 a0001c0001t0032g0084 a0001c0001t0052g0025 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+4774_366+4793d others(22): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10569597 | ||||||
| chr5:10569597 | A | AAAATAAA others(17): Show |
2 | a0001c0001t0006g0024 a0001c0001t0031g0082 |
2 | HG02055.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.366+4770_366+4793d others(26): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10569597 | ||||||
| chr5:10569683 | G | A | 2 | a0001c0001t0006g0012 a0001c0001t0006g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.366+4850G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569683 | |||||||
| chr5:10569717 | C | T | 37 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0060 others(34): Show |
37 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.366+4884C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10569717 | |||||||
| chr5:10570005 | T | C | 1 | a0001c0002t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.366+5172T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570005 | |||||||
| chr5:10570044 | T | G | 2 | a0001c0001t0006g0113 a0006c0018t0035g0112 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+5211T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570044 | |||||||
| chr5:10570065 | C | T | 1 | a0003c0016t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366+5232C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570065 | |||||||
| chr5:10570073 | C | T | 2 | a0001c0001t0006g0296 a0001c0001t0006g0297 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.366+5240C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570073 | |||||||
| chr5:10570488 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.366+5655A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570488 | |||||||
| chr5:10570566 | A | G | 2 | a0001c0002t0027g0070 a0002c0012t0034g0071 |
2 | HG01358.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.366+5733A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570566 | |||||||
| chr5:10570578 | G | A | 10 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0015 others(7): Show |
10 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366+5745G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570578 | |||||||
| chr5:10570889 | A | G | 37 | a0001c0001t0001g0115 a0001c0001t0004g0081 a0001c0001t0004g0088 others(34): Show |
37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.366+6056A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570889 | |||||||
| chr5:10570903 | CT | C | 96 | a0001c0001t0001g0027 a0001c0001t0001g0130 a0001c0001t0001g0131 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.366+6088delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10570903 | ||||||
| chr5:10570921 | T | G | 142 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0126 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.366+6088T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10570921 | |||||||
| chr5:10570921 | T | TG | 74 | a0001c0001t0001g0129 a0001c0001t0001g0242 a0001c0001t0001g0244 others(71): Show |
74 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.366+6089dupG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10570921 | ||||||
| chr5:10571000 | T | G | 1 | a0001c0002t0016g0150 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.366+6167T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571000 | |||||||
| chr5:10571000 | T | TTATAACA others(9): Show |
1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+6169_366+6184d others(18): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10571000 | ||||||
| chr5:10571113 | G | A | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.366+6280G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571113 | |||||||
| chr5:10571284 | C | T | 1 | a0001c0001t0067g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.366+6451C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571284 | |||||||
| chr5:10571399 | G | A | 2 | a0001c0001t0013g0196 a0001c0001t0013g0197 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.366+6566G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571399 | |||||||
| chr5:10571454 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.366+6621A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571454 | |||||||
| chr5:10571491 | C | T | 265 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0115 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.366+6658C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571491 | |||||||
| chr5:10571573 | A | G | 305 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0054 others(302): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.366+6740A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571573 | |||||||
| chr5:10571781 | C | T | 71 | a0001c0001t0001g0129 a0001c0001t0001g0242 a0001c0001t0001g0244 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.366+6948C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571781 | |||||||
| chr5:10571839 | C | G | 1 | a0001c0002t0001g0294 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.366+7006C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571839 | |||||||
| chr5:10571861 | G | A | 2 | a0001c0002t0027g0070 a0002c0012t0034g0071 |
2 | HG01358.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.366+7028G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571861 | |||||||
| chr5:10571891 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+7058T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571891 | |||||||
| chr5:10571892 | C | CT | 255 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0115 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.366+7072dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10571892 | ||||||
| chr5:10571892 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+7059C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571892 | |||||||
| chr5:10571909 | A | G | 261 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0115 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.366+7076A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571909 | |||||||
| chr5:10571952 | A | T | 1 | a0001c0021t0011g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.366+7119A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10571952 | |||||||
| chr5:10572001 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.366+7168G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572001 | |||||||
| chr5:10572081 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366+7248G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572081 | |||||||
| chr5:10572179 | A | G | 305 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0054 others(302): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.366+7346A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572179 | |||||||
| chr5:10572648 | C | T | 1 | a0001c0001t0005g0241 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.366+7815C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572648 | |||||||
| chr5:10572663 | C | T | 2 | a0001c0001t0006g0012 a0001c0001t0006g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.366+7830C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572663 | |||||||
| chr5:10572700 | T | G | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+7867T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572700 | |||||||
| chr5:10572774 | C | T | 3 | a0001c0001t0059g0021 a0001c0006t0058g0023 a0001c0034t0001g0022 |
3 | HG00639.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.366+7941C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572774 | |||||||
| chr5:10572803 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+7970C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572803 | |||||||
| chr5:10572822 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+7989A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572822 | |||||||
| chr5:10572872 | A | G | 29 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0062 others(26): Show |
29 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.366+8039A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572872 | |||||||
| chr5:10572880 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+8047C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10572880 | |||||||
| chr5:10573006 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0009g0201 a0001c0001t0009g0202 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+8173G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573006 | |||||||
| chr5:10573047 | A | G | 1 | a0001c0004t0002g0298 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.366+8214A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573047 | |||||||
| chr5:10573106 | C | T | 1 | a0001c0001t0033g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366+8273C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573106 | |||||||
| chr5:10573197 | GGTGGCTC others(1604): Show |
G | 1 | a0003c0019t0028g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.366+8401_366+10011 others(3): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10573197 | ||||||
| chr5:10573234 | C | T | 1 | a0001c0021t0011g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.366+8401C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573234 | |||||||
| chr5:10573393 | C | T | 2 | a0001c0001t0006g0113 a0006c0018t0035g0112 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+8560C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573393 | |||||||
| chr5:10573402 | G | A | 303 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0054 others(300): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.366+8569G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573402 | |||||||
| chr5:10573443 | G | A | 1 | a0001c0001t0013g0035 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.366+8610G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573443 | |||||||
| chr5:10573451 | G | A | 5 | a0001c0001t0001g0076 a0001c0002t0001g0073 a0001c0002t0050g0078 others(2): Show |
5 | HG03041.hp2 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+8618G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573451 | |||||||
| chr5:10573467 | C | CA | 67 | a0001c0001t0001g0222 a0001c0001t0001g0242 a0001c0001t0001g0244 others(64): Show |
67 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.366+8653dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10573467 | ||||||
| chr5:10573467 | C | CAA | 6 | a0001c0001t0001g0248 a0001c0001t0001g0274 a0001c0002t0001g0255 others(3): Show |
6 | HG02027.hp2 HG02056.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+8652_366+8653d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10573467 | ||||||
| chr5:10573467 | CA | C | 43 | a0001c0001t0001g0065 a0001c0001t0001g0115 a0001c0001t0004g0088 others(40): Show |
43 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.366+8653delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10573467 | ||||||
| chr5:10573480 | A | C | 33 | a0001c0001t0001g0115 a0001c0001t0004g0088 a0001c0001t0004g0090 others(30): Show |
33 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.366+8647A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573480 | |||||||
| chr5:10573720 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.366+8887A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10573720 | |||||||
| chr5:10574063 | C | T | 1 | a0001c0003t0007g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.366+9230C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574063 | |||||||
| chr5:10574231 | A | G | 225 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0121 others(222): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.366+9398A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574231 | |||||||
| chr5:10574261 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.366+9428T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574261 | |||||||
| chr5:10574425 | A | G | 1 | a0001c0002t0001g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.366+9592A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574425 | |||||||
| chr5:10574639 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.366+9806C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574639 | |||||||
| chr5:10574704 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+9871C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574704 | |||||||
| chr5:10574845 | T | C | 247 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0060 others(244): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.366+10012T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574845 | |||||||
| chr5:10574847 | AAGCGGGA others(329): Show |
A | 247 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0060 others(244): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.366+10015_366+1035 others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574847 | |||||||
| chr5:10574850 | C | T | 14 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0115 others(11): Show |
14 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.366+10017C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574850 | |||||||
| chr5:10574939 | T | C | 9 | a0001c0001t0001g0238 a0001c0001t0006g0024 a0001c0001t0052g0025 others(6): Show |
9 | HG01069.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+10106T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10574939 | |||||||
| chr5:10575095 | C | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0066 others(37): Show |
40 | HG00733.hp2 HG01069.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.366+10262C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575095 | |||||||
| chr5:10575172 | G | C | 66 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0065 others(63): Show |
66 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.366+10339G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575172 | |||||||
| chr5:10575186 | A | T | 246 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0060 others(243): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.366+10353A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575186 | |||||||
| chr5:10575189 | C | G | 246 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0060 others(243): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.366+10356C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575189 | |||||||
| chr5:10575227 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0004g0088 |
2 | HG02015.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.366+10394G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575227 | |||||||
| chr5:10575298 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+10465T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575298 | |||||||
| chr5:10575415 | A | ACT | 305 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0054 others(302): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.366+10583_366+1058 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10575415 | ||||||
| chr5:10575422 | CA | C | 17 | a0001c0001t0001g0121 a0001c0001t0001g0138 a0001c0001t0001g0142 others(14): Show |
17 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.366+10605delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10575422 | ||||||
| chr5:10575745 | T | C | 303 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(300): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.366+10912T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575745 | |||||||
| chr5:10575782 | C | T | 2 | a0001c0001t0006g0113 a0006c0018t0035g0112 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+10949C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10575782 | |||||||
| chr5:10575978 | T | TAC | 34 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0156 others(31): Show |
34 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.366+11164_366+1116 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10575978 | ||||||
| chr5:10575978 | T | TACACAC | 34 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(31): Show |
34 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.366+11160_366+1116 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10575978 | ||||||
| chr5:10575978 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+11156_366+1116 others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10575978 | ||||||
| chr5:10576125 | A | G | 32 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0115 others(29): Show |
32 | HG00733.hp2 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.366+11292A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576125 | |||||||
| chr5:10576186 | G | A | 1 | a0001c0004t0002g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.366+11353G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576186 | |||||||
| chr5:10576220 | A | G | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+11387A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576220 | |||||||
| chr5:10576352 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+11519C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576352 | |||||||
| chr5:10576650 | A | G | 1 | a0001c0002t0001g0294 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.366+11817A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576650 | |||||||
| chr5:10576655 | G | A | 1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.366+11822G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576655 | |||||||
| chr5:10576806 | G | A | 1 | a0001c0005t0002g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.366+11973G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10576806 | |||||||
| chr5:10577018 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.366+12185G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577018 | |||||||
| chr5:10577030 | G | C | 1 | a0002c0010t0018g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.366+12197G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577030 | |||||||
| chr5:10577085 | TCCCTTTC others(11): Show |
T | 1 | a0001c0003t0007g0254 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.366+12276_366+1229 others(22): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10577085 | ||||||
| chr5:10577097 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.366+12264C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577097 | |||||||
| chr5:10577109 | T | TCCCTTC | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+12294_366+1229 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10577109 | ||||||
| chr5:10577223 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.366+12390G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577223 | |||||||
| chr5:10577275 | A | G | 103 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0121 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.366+12442A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577275 | |||||||
| chr5:10577290 | T | C | 304 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(301): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.366+12457T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577290 | |||||||
| chr5:10577422 | C | G | 10 | a0001c0001t0001g0187 a0001c0001t0001g0310 a0001c0001t0001g0311 others(7): Show |
10 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.366+12589C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577422 | |||||||
| chr5:10577622 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.366+12789C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577622 | |||||||
| chr5:10577623 | G | A | 1 | a0002c0012t0034g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.366+12790G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577623 | |||||||
| chr5:10577694 | T | G | 2 | a0001c0001t0006g0113 a0006c0018t0035g0112 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+12861T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577694 | |||||||
| chr5:10577783 | C | T | 294 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.366+12950C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577783 | |||||||
| chr5:10577872 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.366+13039G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577872 | |||||||
| chr5:10577918 | G | A | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+13085G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10577918 | |||||||
| chr5:10578014 | T | G | 1 | a0001c0002t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.366+13181T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578014 | |||||||
| chr5:10578191 | G | A | 296 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.366+13358G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578191 | |||||||
| chr5:10578330 | G | A | 99 | a0001c0001t0001g0060 a0001c0001t0001g0126 a0001c0001t0001g0156 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.366+13497G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578330 | |||||||
| chr5:10578453 | T | G | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+13620T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578453 | |||||||
| chr5:10578560 | C | T | 53 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(50): Show |
53 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.366+13727C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578560 | |||||||
| chr5:10578650 | T | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.366+13817T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578650 | |||||||
| chr5:10578677 | C | T | 1 | a0001c0009t0008g0313 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.366+13844C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578677 | |||||||
| chr5:10578763 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.366+13930A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578763 | |||||||
| chr5:10578769 | A | G | 297 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(294): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.366+13936A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578769 | |||||||
| chr5:10578835 | T | A | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.366+14002T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578835 | |||||||
| chr5:10578862 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.366+14029A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578862 | |||||||
| chr5:10578916 | C | T | 2 | a0001c0001t0001g0290 a0001c0003t0007g0254 |
2 | NA18948.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.366+14083C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10578916 | |||||||
| chr5:10579119 | G | A | 1 | a0001c0004t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.366+14286G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579119 | |||||||
| chr5:10579164 | CA | C | 184 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0065 others(181): Show |
184 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.366+14348delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10579164 | ||||||
| chr5:10579211 | C | T | 297 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(294): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.366+14378C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579211 | |||||||
| chr5:10579248 | A | T | 1 | a0001c0001t0033g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366+14415A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579248 | |||||||
| chr5:10579353 | GT | G | 114 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0076 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.366+14533delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10579353 | ||||||
| chr5:10579586 | G | A | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.366+14753G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579586 | |||||||
| chr5:10579594 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.366+14761A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579594 | |||||||
| chr5:10579602 | T | C | 53 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(50): Show |
53 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.366+14769T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579602 | |||||||
| chr5:10579706 | A | T | 2 | a0001c0030t0019g0199 a0005c0017t0021g0127 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.366+14873A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579706 | |||||||
| chr5:10579786 | T | A | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.366+14953T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579786 | |||||||
| chr5:10579853 | A | G | 24 | a0001c0001t0001g0076 a0001c0001t0001g0308 a0001c0001t0004g0081 others(21): Show |
24 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.366+15020A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579853 | |||||||
| chr5:10579962 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.366+15129C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10579962 | |||||||
| chr5:10580094 | CT | C | 12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0029g0239 others(9): Show |
12 | HG00733.hp2 HG01074.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.366+15262delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580094 | |||||||
| chr5:10580195 | C | T | 2 | a0001c0002t0001g0073 a0007c0022t0020g0005 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.366+15362C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580195 | |||||||
| chr5:10580368 | A | G | 1 | a0001c0015t0001g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.366+15535A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580368 | |||||||
| chr5:10580512 | CA | C | 31 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0249 others(28): Show |
31 | HG00438.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.366+15680delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580512 | |||||||
| chr5:10580513 | A | C | 5 | a0001c0001t0001g0308 a0001c0002t0001g0072 a0001c0009t0008g0304 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+15680A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580513 | |||||||
| chr5:10580517 | T | C | 31 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0249 others(28): Show |
31 | HG00438.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.366+15684T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580517 | |||||||
| chr5:10580829 | C | T | 294 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.366+15996C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10580829 | |||||||
| chr5:10581012 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.366+16179G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581012 | |||||||
| chr5:10581232 | G | C | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+16399G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581232 | |||||||
| chr5:10581265 | G | C | 1 | a0001c0003t0060g0093 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.366+16432G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581265 | |||||||
| chr5:10581379 | G | A | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+16546G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581379 | |||||||
| chr5:10581407 | G | A | 1 | a0001c0001t0052g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.366+16574G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581407 | |||||||
| chr5:10581430 | G | A | 2 | a0001c0005t0023g0223 a0001c0005t0023g0233 |
2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.366+16597G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581430 | |||||||
| chr5:10581490 | C | G | 54 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(51): Show |
54 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.366+16657C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581490 | |||||||
| chr5:10581505 | C | T | 6 | a0001c0002t0001g0230 a0001c0002t0050g0078 a0001c0006t0058g0023 others(3): Show |
6 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+16672C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581505 | |||||||
| chr5:10581544 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+16711C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581544 | |||||||
| chr5:10581640 | G | C | 9 | a0001c0001t0004g0081 a0001c0001t0012g0016 a0001c0001t0012g0019 others(6): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+16807G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581640 | |||||||
| chr5:10581718 | C | T | 276 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.366+16885C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581718 | |||||||
| chr5:10581970 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.366+17137G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10581970 | |||||||
| chr5:10582134 | C | T | 3 | a0001c0001t0004g0081 a0001c0004t0002g0293 a0001c0025t0019g0002 |
3 | HG03540.hp2 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.366+17301C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582134 | |||||||
| chr5:10582380 | G | A | 1 | a0008c0036t0001g0047 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.366+17547G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582380 | |||||||
| chr5:10582394 | G | A | 3 | a0003c0016t0001g0006 a0003c0016t0001g0010 a0003c0035t0001g0122 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.366+17561G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582394 | |||||||
| chr5:10582427 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+17594T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582427 | |||||||
| chr5:10582465 | C | T | 106 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(103): Show |
106 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.366+17632C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582465 | |||||||
| chr5:10582555 | A | C | 1 | a0001c0003t0007g0254 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.366+17722A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582555 | |||||||
| chr5:10582593 | C | G | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.366+17760C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582593 | |||||||
| chr5:10582676 | G | T | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+17843G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582676 | |||||||
| chr5:10582681 | G | A | 2 | a0001c0004t0002g0058 a0001c0006t0007g0059 |
2 | HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.366+17848G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582681 | |||||||
| chr5:10582747 | G | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0281 a0001c0001t0042g0198 others(4): Show |
7 | HG00280.hp1 HG01123.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+17914G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582747 | |||||||
| chr5:10582753 | C | T | 4 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0001c0030t0019g0199 others(1): Show |
4 | HG02280.hp1 HG02683.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+17920C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582753 | |||||||
| chr5:10582823 | G | A | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.366+17990G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10582823 | |||||||
| chr5:10582989 | CT | C | 189 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0065 others(186): Show |
189 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.366+18172delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10582989 | ||||||
| chr5:10583003 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.366+18170T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583003 | |||||||
| chr5:10583275 | C | T | 1 | a0001c0013t0011g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.366+18442C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583275 | |||||||
| chr5:10583289 | C | T | 228 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0060 others(225): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.366+18456C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583289 | |||||||
| chr5:10583380 | G | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+18547G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583380 | |||||||
| chr5:10583425 | G | A | 121 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.366+18592G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583425 | |||||||
| chr5:10583517 | G | A | 4 | a0001c0002t0001g0230 a0001c0002t0050g0078 a0001c0006t0058g0023 others(1): Show |
4 | HG00639.hp2 HG02109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+18684G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583517 | |||||||
| chr5:10583664 | C | T | 1 | a0001c0005t0002g0055 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.366+18831C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583664 | |||||||
| chr5:10583703 | G | GT | 89 | a0001c0001t0001g0060 a0001c0001t0001g0156 a0001c0001t0001g0162 others(86): Show |
89 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.366+18876dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10583703 | ||||||
| chr5:10583735 | G | A | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+18902G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583735 | |||||||
| chr5:10583849 | G | A | 1 | a0001c0005t0063g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.366+19016G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583849 | |||||||
| chr5:10583948 | C | T | 108 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(105): Show |
108 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.366+19115C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583948 | |||||||
| chr5:10583959 | A | G | 1 | a0001c0001t0009g0316 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.366+19126A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583959 | |||||||
| chr5:10583963 | A | C | 2 | a0001c0002t0001g0068 a0001c0005t0002g0067 |
2 | HG00733.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.366+19130A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10583963 | |||||||
| chr5:10584166 | A | G | 2 | a0001c0001t0042g0198 a0001c0002t0016g0150 |
2 | HG01123.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.366+19333A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584166 | |||||||
| chr5:10584389 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+19556T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584389 | |||||||
| chr5:10584460 | C | CA | 16 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0001t0033g0103 others(13): Show |
16 | HG01069.hp1 HG02055.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.366+19628dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10584460 | ||||||
| chr5:10584558 | A | T | 127 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.366+19725A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584558 | |||||||
| chr5:10584597 | G | A | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+19764G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584597 | |||||||
| chr5:10584670 | C | T | 113 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.366+19837C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584670 | |||||||
| chr5:10584689 | C | T | 2 | a0001c0001t0049g0321 a0001c0006t0003g0132 |
2 | HG01106.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.366+19856C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584689 | |||||||
| chr5:10584726 | G | T | 1 | a0001c0004t0002g0293 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.366+19893G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584726 | |||||||
| chr5:10584768 | A | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+19935A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584768 | |||||||
| chr5:10584843 | G | A | 1 | a0001c0025t0019g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.366+20010G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584843 | |||||||
| chr5:10584972 | G | A | 1 | a0001c0037t0002g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.366+20139G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584972 | |||||||
| chr5:10584974 | T | C | 1 | a0001c0003t0003g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.366+20141T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584974 | |||||||
| chr5:10584999 | A | C | 51 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(48): Show |
51 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.366+20166A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10584999 | |||||||
| chr5:10585044 | A | G | 288 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.366+20211A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585044 | |||||||
| chr5:10585097 | G | A | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+20264G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585097 | |||||||
| chr5:10585175 | G | A | 288 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.366+20342G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585175 | |||||||
| chr5:10585177 | C | T | 5 | a0001c0001t0005g0118 a0001c0001t0005g0182 a0001c0001t0005g0241 others(2): Show |
5 | HG02080.hp2 NA18949.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.366+20344C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585177 | |||||||
| chr5:10585258 | C | T | 104 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(101): Show |
104 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.366+20425C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585258 | |||||||
| chr5:10585287 | A | G | 1 | a0001c0001t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.366+20454A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585287 | |||||||
| chr5:10585287 | A | T | 54 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(51): Show |
54 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.366+20454A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585287 | |||||||
| chr5:10585531 | G | A | 113 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.366+20698G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585531 | |||||||
| chr5:10585554 | C | G | 1 | a0002c0012t0034g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.366+20721C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585554 | |||||||
| chr5:10585751 | A | G | 288 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.366+20918A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585751 | |||||||
| chr5:10585875 | C | G | 2 | a0001c0026t0008g0008 a0001c0031t0062g0114 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.366+21042C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585875 | |||||||
| chr5:10585887 | G | T | 2 | a0001c0004t0002g0058 a0001c0006t0007g0059 |
2 | HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.366+21054G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585887 | |||||||
| chr5:10585949 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+21116C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585949 | |||||||
| chr5:10585984 | C | T | 1 | a0001c0002t0043g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.366+21151C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10585984 | |||||||
| chr5:10586223 | A | G | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+21390A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586223 | |||||||
| chr5:10586361 | C | T | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.366+21528C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586361 | |||||||
| chr5:10586457 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.366+21624G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586457 | |||||||
| chr5:10586485 | C | CTG | 12 | a0001c0001t0001g0249 a0001c0001t0004g0090 a0001c0001t0065g0102 others(9): Show |
12 | HG01884.hp1 HG02080.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.366+21700_366+2170 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTG | C | 13 | a0001c0001t0001g0032 a0001c0001t0001g0129 a0001c0001t0001g0180 others(10): Show |
13 | HG00438.hp1 HG02015.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.366+21700_366+2170 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTG | C | 35 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0054 others(32): Show |
35 | HG00280.hp1 HG00741.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.366+21698_366+2170 others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTG | C | 113 | a0001c0001t0001g0062 a0001c0001t0001g0115 a0001c0001t0001g0142 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.366+21696_366+2170 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(1): Show |
C | 47 | a0001c0001t0001g0060 a0001c0001t0001g0138 a0001c0001t0001g0190 others(44): Show |
47 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.366+21694_366+2170 others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(3): Show |
C | 49 | a0001c0001t0001g0171 a0001c0001t0001g0222 a0001c0001t0001g0237 others(46): Show |
49 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.366+21692_366+2170 others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(5): Show |
C | 16 | a0001c0001t0001g0066 a0001c0001t0001g0130 a0001c0001t0001g0163 others(13): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.366+21690_366+2170 others(16): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(9): Show |
C | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.366+21686_366+2170 others(20): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(11): Show |
C | 2 | a0001c0001t0026g0210 a0001c0002t0001g0230 |
2 | HG02109.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.366+21684_366+2170 others(22): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(13): Show |
C | 1 | a0001c0006t0003g0267 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.366+21682_366+2170 others(24): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586485 | CTGTGTGT others(17): Show |
C | 6 | a0001c0001t0001g0065 a0001c0001t0001g0308 a0001c0002t0001g0068 others(3): Show |
6 | HG00733.hp2 HG01258.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+21678_366+2170 others(28): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586485 | ||||||
| chr5:10586521 | GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0001g0255 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.366+21690_366+2170 others(18): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586521 | ||||||
| chr5:10586523 | GTGTGTGT others(5): Show |
G | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.366+21692_366+2170 others(16): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586523 | ||||||
| chr5:10586628 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.366+21795A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586628 | |||||||
| chr5:10586650 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+21817A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586650 | |||||||
| chr5:10586679 | T | C | 1 | a0001c0001t0056g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.366+21846T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586679 | |||||||
| chr5:10586751 | A | G | 1 | a0001c0006t0058g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.366+21918A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586751 | |||||||
| chr5:10586881 | G | C | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.366+22048G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586881 | |||||||
| chr5:10586891 | A | T | 105 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(102): Show |
105 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.366+22058A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586891 | |||||||
| chr5:10586894 | T | TAAGAAAT others(319): Show |
1 | a0001c0002t0046g0177 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.366+22072_366+2207 others(330): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10586894 | ||||||
| chr5:10586935 | G | A | 5 | a0001c0002t0004g0096 a0001c0002t0004g0097 a0001c0002t0004g0098 others(2): Show |
5 | NA18964.hp2 NA18967.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+22102G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10586935 | |||||||
| chr5:10587005 | A | ATTAT | 32 | a0001c0001t0001g0054 a0001c0001t0001g0190 a0001c0001t0001g0244 others(29): Show |
32 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.366+22195_366+2219 others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10587005 | ||||||
| chr5:10587005 | A | ATTATTTA others(1): Show |
23 | a0001c0001t0001g0291 a0001c0001t0001g0305 a0001c0001t0006g0015 others(20): Show |
23 | HG01243.hp2 HG01255.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.366+22191_366+2219 others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10587005 | ||||||
| chr5:10587054 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.366+22221G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587054 | |||||||
| chr5:10587078 | G | A | 1 | a0001c0002t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.366+22245G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587078 | |||||||
| chr5:10587122 | C | T | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.366+22289C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587122 | |||||||
| chr5:10587176 | G | A | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+22343G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587176 | |||||||
| chr5:10587195 | A | G | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.366+22362A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587195 | |||||||
| chr5:10587267 | AT | A | 54 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(51): Show |
54 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.366+22439delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10587267 | ||||||
| chr5:10587344 | G | A | 4 | a0001c0002t0001g0045 a0001c0002t0001g0175 a0001c0004t0002g0227 others(1): Show |
4 | HG01099.hp1 HG01358.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+22511G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587344 | |||||||
| chr5:10587548 | AT | A | 8 | a0001c0001t0001g0126 a0001c0001t0006g0012 a0001c0001t0006g0013 others(5): Show |
8 | HG02280.hp1 HG02683.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+22728delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10587548 | ||||||
| chr5:10587661 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.366+22828G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587661 | |||||||
| chr5:10587698 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.366+22865T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587698 | |||||||
| chr5:10587731 | C | G | 1 | a0001c0003t0003g0053 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.366+22898C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587731 | |||||||
| chr5:10587747 | G | T | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.366+22914G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587747 | |||||||
| chr5:10587921 | C | T | 295 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.366+23088C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10587921 | |||||||
| chr5:10588088 | G | A | 1 | a0002c0010t0036g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.366+23255G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588088 | |||||||
| chr5:10588279 | A | G | 107 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(104): Show |
107 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.366+23446A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588279 | |||||||
| chr5:10588321 | T | G | 1 | a0001c0001t0031g0082 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.366+23488T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588321 | |||||||
| chr5:10588474 | A | ATTGTTAG others(8): Show |
1 | a0010c0029t0041g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.366+23643_366+2365 others(19): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10588474 | ||||||
| chr5:10588599 | G | C | 112 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.366+23766G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588599 | |||||||
| chr5:10588702 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.366+23869A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588702 | |||||||
| chr5:10588709 | A | C | 6 | a0001c0001t0001g0203 a0001c0001t0009g0201 a0001c0001t0009g0202 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+23876A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588709 | |||||||
| chr5:10588785 | C | A | 116 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.366+23952C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588785 | |||||||
| chr5:10588903 | C | T | 4 | a0001c0002t0001g0230 a0001c0002t0050g0078 a0001c0006t0058g0023 others(1): Show |
4 | HG00639.hp2 HG02109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+24070C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10588903 | |||||||
| chr5:10589190 | C | A | 1 | a0001c0002t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.366+24357C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589190 | |||||||
| chr5:10589221 | C | T | 1 | a0001c0001t0049g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.366+24388C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589221 | |||||||
| chr5:10589253 | G | GCAGGTCC others(12): Show |
1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.366+24436_366+2443 others(23): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10589253 | ||||||
| chr5:10589300 | G | T | 20 | a0001c0001t0001g0291 a0001c0001t0001g0305 a0001c0001t0006g0113 others(17): Show |
20 | HG01255.hp1 HG01361.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+24467G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589300 | |||||||
| chr5:10589318 | C | G | 4 | a0001c0001t0001g0301 a0001c0003t0003g0145 a0001c0003t0003g0153 others(1): Show |
4 | HG02165.hp1 NA18944.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+24485C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589318 | |||||||
| chr5:10589380 | C | G | 1 | a0001c0002t0053g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.366+24547C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589380 | |||||||
| chr5:10589390 | C | T | 105 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(102): Show |
105 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.366+24557C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589390 | |||||||
| chr5:10589832 | A | G | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+24999A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589832 | |||||||
| chr5:10589850 | A | G | 1 | a0001c0003t0003g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.366+25017A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589850 | |||||||
| chr5:10589888 | C | T | 1 | a0001c0025t0019g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.366+25055C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589888 | |||||||
| chr5:10589963 | T | A | 2 | a0001c0001t0052g0025 a0001c0009t0008g0313 |
2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.366+25130T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10589963 | |||||||
| chr5:10590072 | A | G | 106 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(103): Show |
106 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.366+25239A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590072 | |||||||
| chr5:10590115 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+25282A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590115 | |||||||
| chr5:10590172 | G | C | 112 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.366+25339G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590172 | |||||||
| chr5:10590194 | G | A | 1 | a0001c0025t0019g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.366+25361G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590194 | |||||||
| chr5:10590400 | C | T | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+25567C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590400 | |||||||
| chr5:10590414 | A | C | 88 | a0001c0001t0001g0060 a0001c0001t0001g0156 a0001c0001t0001g0162 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.366+25581A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590414 | |||||||
| chr5:10590468 | A | G | 292 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.366+25635A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590468 | |||||||
| chr5:10590472 | C | A | 2 | a0001c0001t0068g0204 a0001c0003t0007g0309 |
2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.366+25639C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590472 | |||||||
| chr5:10590583 | T | A | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+25750T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590583 | |||||||
| chr5:10590589 | TGC | T | 74 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0156 others(71): Show |
74 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.366+25774_366+2577 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590589 | ||||||
| chr5:10590589 | TGCGC | T | 4 | a0001c0001t0001g0126 a0001c0001t0004g0094 a0001c0003t0007g0309 others(1): Show |
4 | HG03139.hp1 HG03540.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+25772_366+2577 others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590589 | ||||||
| chr5:10590589 | TGCGCGC | T | 100 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.366+25770_366+2577 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590589 | ||||||
| chr5:10590601 | CGCGCGCG others(1): Show |
C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(6): Show |
9 | HG00733.hp2 HG01106.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+25770_366+2577 others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590601 | ||||||
| chr5:10590601 | CGCGCGCG others(3): Show |
C | 50 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(47): Show |
50 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.366+25770_366+2577 others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590601 | ||||||
| chr5:10590601 | CGCGCGCG others(5): Show |
C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.366+25770_366+2578 others(16): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590601 | ||||||
| chr5:10590603 | CGCGCGT | C | 18 | a0001c0001t0001g0184 a0001c0001t0001g0242 a0001c0001t0001g0268 others(15): Show |
18 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.366+25772_366+2577 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590603 | ||||||
| chr5:10590605 | CGCGTGT | C | 6 | a0001c0002t0001g0230 a0001c0002t0050g0078 a0001c0006t0058g0023 others(3): Show |
6 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+25774_366+2577 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10590605 | ||||||
| chr5:10590607 | C | T | 25 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0308 others(22): Show |
25 | HG00438.hp2 HG00738.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.366+25774C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590607 | |||||||
| chr5:10590609 | T | C | 2 | a0001c0004t0002g0256 a0001c0004t0002g0298 |
2 | HG01192.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.366+25776T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590609 | |||||||
| chr5:10590620 | G | T | 2 | a0001c0026t0008g0008 a0001c0031t0062g0114 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.366+25787G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590620 | |||||||
| chr5:10590649 | G | T | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+25816G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590649 | |||||||
| chr5:10590764 | C | T | 5 | a0001c0001t0033g0103 a0001c0011t0012g0003 a0001c0014t0008g0128 others(2): Show |
5 | HG01069.hp1 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+25931C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590764 | |||||||
| chr5:10590895 | G | C | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.366+26062G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590895 | |||||||
| chr5:10590911 | C | T | 1 | a0001c0003t0007g0276 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.366+26078C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590911 | |||||||
| chr5:10590964 | G | C | 2 | a0001c0001t0005g0185 a0001c0003t0003g0186 |
2 | NA18941.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.366+26131G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10590964 | |||||||
| chr5:10591020 | G | C | 112 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.366+26187G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591020 | |||||||
| chr5:10591055 | C | T | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+26222C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591055 | |||||||
| chr5:10591056 | A | G | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+26223A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591056 | |||||||
| chr5:10591123 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.366+26290C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591123 | |||||||
| chr5:10591194 | G | GTTTTTT | 6 | a0001c0001t0001g0115 a0001c0001t0006g0012 a0001c0001t0006g0013 others(3): Show |
6 | HG01074.hp2 HG01884.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+26361_366+2636 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591194 | |||||||
| chr5:10591194 | G | GTTTTTTT | 57 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0190 others(54): Show |
57 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.366+26361_366+2636 others(11): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591194 | |||||||
| chr5:10591194 | G | GTTTTTTT others(1): Show |
102 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(99): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.366+26361_366+2636 others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591194 | |||||||
| chr5:10591194 | G | GTTTTTTT others(2): Show |
21 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0138 others(18): Show |
21 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.366+26361_366+2636 others(13): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591194 | |||||||
| chr5:10591194 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0184 a0001c0002t0001g0157 a0001c0003t0060g0093 |
3 | HG02738.hp2 NA19064.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.366+26361_366+2636 others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591194 | |||||||
| chr5:10591195 | G | T | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+26362G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591195 | |||||||
| chr5:10591195 | GT | G | 103 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0156 others(100): Show |
103 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.366+26377delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10591195 | ||||||
| chr5:10591228 | G | T | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+26395G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591228 | |||||||
| chr5:10591278 | C | T | 1 | a0001c0037t0002g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.366+26445C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591278 | |||||||
| chr5:10591360 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+26527T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591360 | |||||||
| chr5:10591542 | CA | C | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+26711delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10591542 | ||||||
| chr5:10591560 | G | A | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.366+26727G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591560 | |||||||
| chr5:10591586 | T | C | 295 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.367-26747T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591586 | |||||||
| chr5:10591663 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.367-26670A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591663 | |||||||
| chr5:10591679 | C | G | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.367-26654C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591679 | |||||||
| chr5:10591695 | T | C | 2 | a0001c0003t0003g0056 a0001c0003t0003g0057 |
2 | NA18953.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.367-26638T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591695 | |||||||
| chr5:10591814 | G | GTTTATA | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.367-26515_367-2651 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10591814 | ||||||
| chr5:10591970 | T | A | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.367-26363T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591970 | |||||||
| chr5:10591970 | T | C | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.367-26363T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591970 | |||||||
| chr5:10591976 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.367-26357A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591976 | |||||||
| chr5:10591981 | T | C | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.367-26352T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10591981 | |||||||
| chr5:10592016 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.367-26317T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10592016 | |||||||
| chr5:10592073 | GGT | G | 104 | a0001c0001t0001g0076 a0001c0001t0001g0126 a0001c0001t0001g0156 others(101): Show |
104 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.367-26235_367-2623 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592073 | ||||||
| chr5:10592073 | GGTGTGT | G | 187 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.367-26239_367-2623 others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592073 | ||||||
| chr5:10592338 | C | T | 189 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.367-25995C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10592338 | |||||||
| chr5:10592369 | T | C | 106 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(103): Show |
106 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.367-25964T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10592369 | |||||||
| chr5:10592450 | T | TA | 37 | a0001c0001t0001g0054 a0001c0001t0001g0156 a0001c0001t0001g0166 others(34): Show |
37 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.367-25856dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592450 | ||||||
| chr5:10592450 | T | TAA | 7 | a0001c0001t0001g0211 a0001c0001t0009g0034 a0001c0001t0029g0239 others(4): Show |
7 | HG01074.hp2 HG01169.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-25857_367-2585 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592450 | ||||||
| chr5:10592450 | TA | T | 33 | a0001c0001t0001g0066 a0001c0001t0001g0138 a0001c0001t0005g0185 others(30): Show |
33 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.367-25856delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592450 | ||||||
| chr5:10592450 | TAA | T | 125 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.367-25857_367-2585 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592450 | ||||||
| chr5:10592450 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.367-25865_367-2585 others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592450 | ||||||
| chr5:10592495 | C | T | 6 | a0001c0002t0001g0230 a0001c0002t0050g0078 a0001c0006t0058g0023 others(3): Show |
6 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-25838C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10592495 | |||||||
| chr5:10592606 | A | G | 155 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.367-25727A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10592606 | |||||||
| chr5:10592624 | C | CA | 134 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(131): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.367-25696dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592624 | ||||||
| chr5:10592626 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0274 a0001c0007t0001g0160 |
2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.367-25704_367-2569 others(16): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10592626 | ||||||
| chr5:10592979 | A | G | 1 | a0006c0018t0061g0087 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.367-25354A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10592979 | |||||||
| chr5:10593047 | C | T | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0009g0034 others(6): Show |
9 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-25286C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593047 | |||||||
| chr5:10593049 | T | C | 298 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(295): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.367-25284T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593049 | |||||||
| chr5:10593178 | CTTATA | C | 115 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.367-25149_367-2514 others(9): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10593178 | ||||||
| chr5:10593205 | TAGTTG | T | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.367-25124_367-2512 others(9): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10593205 | ||||||
| chr5:10593224 | A | G | 115 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.367-25109A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593224 | |||||||
| chr5:10593233 | C | A | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.367-25100C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593233 | |||||||
| chr5:10593255 | A | G | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.367-25078A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593255 | |||||||
| chr5:10593257 | A | G | 1 | a0001c0021t0011g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.367-25076A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593257 | |||||||
| chr5:10593325 | C | T | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.367-25008C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593325 | |||||||
| chr5:10593596 | A | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0048g0117 others(6): Show |
9 | HG00733.hp2 HG01175.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-24737A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593596 | |||||||
| chr5:10593643 | A | C | 297 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(294): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.367-24690A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593643 | |||||||
| chr5:10593663 | AC | A | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24668delC | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10593663 | ||||||
| chr5:10593665 | C | G | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24668C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593665 | |||||||
| chr5:10593668 | T | A | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24665T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593668 | |||||||
| chr5:10593669 | T | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24664T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593669 | |||||||
| chr5:10593704 | G | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367-24629G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593704 | |||||||
| chr5:10593919 | C | T | 1 | a0001c0004t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.367-24414C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593919 | |||||||
| chr5:10593937 | G | A | 2 | a0001c0025t0019g0002 a0002c0028t0037g0007 |
2 | HG01069.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-24396G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593937 | |||||||
| chr5:10593949 | C | T | 119 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(116): Show |
119 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.367-24384C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593949 | |||||||
| chr5:10593968 | T | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24365T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593968 | |||||||
| chr5:10593977 | C | G | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24356C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10593977 | |||||||
| chr5:10594061 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.367-24272C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10594061 | |||||||
| chr5:10594157 | GTATT | G | 58 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(55): Show |
58 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.367-24171_367-2416 others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10594157 | ||||||
| chr5:10594182 | A | G | 58 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(55): Show |
58 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.367-24151A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10594182 | |||||||
| chr5:10594221 | C | CT | 195 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0060 others(192): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.367-24089dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10594221 | ||||||
| chr5:10594221 | C | CTT | 16 | a0001c0001t0001g0076 a0001c0001t0001g0203 a0001c0001t0004g0094 others(13): Show |
16 | HG00639.hp1 HG00642.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.367-24090_367-2408 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10594221 | ||||||
| chr5:10594221 | C | CTTT | 10 | a0001c0001t0006g0024 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-24091_367-2408 others(7): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10594221 | ||||||
| chr5:10594221 | CT | C | 53 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(50): Show |
53 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.367-24089delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10594221 | ||||||
| chr5:10594221 | CTT | C | 7 | a0001c0001t0001g0291 a0001c0001t0006g0296 a0001c0004t0002g0058 others(4): Show |
7 | HG01069.hp1 HG02280.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-24090_367-2408 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10594221 | ||||||
| chr5:10594310 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0003t0017g0080 |
3 | HG02698.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.367-24023C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10594310 | |||||||
| chr5:10594311 | G | A | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-24022G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10594311 | |||||||
| chr5:10595054 | A | G | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-23279A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595054 | |||||||
| chr5:10595161 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.367-23172G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595161 | |||||||
| chr5:10595166 | T | A | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.367-23167T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595166 | |||||||
| chr5:10595219 | G | A | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-23114G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595219 | |||||||
| chr5:10595338 | G | A | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.367-22995G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595338 | |||||||
| chr5:10595649 | C | T | 2 | a0001c0030t0019g0199 a0005c0017t0021g0127 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.367-22684C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595649 | |||||||
| chr5:10595869 | C | T | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-22464C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595869 | |||||||
| chr5:10595906 | G | A | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-22427G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595906 | |||||||
| chr5:10595971 | T | C | 1 | a0001c0005t0002g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.367-22362T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10595971 | |||||||
| chr5:10596157 | G | T | 137 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(134): Show |
137 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.367-22176G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596157 | |||||||
| chr5:10596318 | T | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-22015T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596318 | |||||||
| chr5:10596324 | A | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-22009A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596324 | |||||||
| chr5:10596350 | A | T | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-21983A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596350 | |||||||
| chr5:10596367 | T | C | 123 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(120): Show |
123 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.367-21966T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596367 | |||||||
| chr5:10596381 | C | T | 1 | a0001c0003t0007g0276 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.367-21952C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596381 | |||||||
| chr5:10596450 | A | G | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-21883A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596450 | |||||||
| chr5:10596530 | T | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-21803T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596530 | |||||||
| chr5:10596635 | T | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-21698T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596635 | |||||||
| chr5:10596797 | GAA | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-21534_367-2153 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10596797 | ||||||
| chr5:10596813 | C | T | 6 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(3): Show |
6 | HG01069.hp1 HG01884.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-21520C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596813 | |||||||
| chr5:10596878 | T | C | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-21455T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596878 | |||||||
| chr5:10596901 | T | C | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-21432T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10596901 | |||||||
| chr5:10597113 | A | T | 8 | a0001c0001t0001g0065 a0001c0001t0048g0117 a0001c0002t0001g0064 others(5): Show |
8 | HG00733.hp2 HG01258.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-21220A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597113 | |||||||
| chr5:10597236 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-21097C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597236 | |||||||
| chr5:10597304 | A | G | 23 | a0001c0001t0001g0291 a0001c0001t0001g0305 a0001c0001t0006g0015 others(20): Show |
23 | HG01106.hp2 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.367-21029A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597304 | |||||||
| chr5:10597363 | G | A | 1 | a0001c0001t0005g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.367-20970G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597363 | |||||||
| chr5:10597509 | G | T | 3 | a0001c0001t0057g0038 a0001c0002t0030g0037 a0001c0002t0030g0039 |
3 | HG03490.hp1 HG03492.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.367-20824G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597509 | |||||||
| chr5:10597583 | A | G | 116 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0076 others(113): Show |
116 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.367-20750A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597583 | |||||||
| chr5:10597607 | C | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-20726C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597607 | |||||||
| chr5:10597747 | T | C | 125 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0076 others(122): Show |
125 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.367-20586T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597747 | |||||||
| chr5:10597749 | C | T | 1 | a0001c0001t0048g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.367-20584C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597749 | |||||||
| chr5:10597874 | G | A | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.367-20459G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597874 | |||||||
| chr5:10597914 | GT | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-20412delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10597914 | ||||||
| chr5:10597916 | T | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-20417T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597916 | |||||||
| chr5:10597982 | A | G | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.367-20351A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10597982 | |||||||
| chr5:10598101 | C | T | 1 | a0001c0005t0002g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.367-20232C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598101 | |||||||
| chr5:10598177 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.367-20156C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598177 | |||||||
| chr5:10598263 | A | ATTTTGTT | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-20058_367-2005 others(11): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10598263 | ||||||
| chr5:10598441 | A | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19892A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598441 | |||||||
| chr5:10598458 | A | G | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.367-19875A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598458 | |||||||
| chr5:10598470 | T | C | 1 | a0001c0020t0044g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.367-19863T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598470 | |||||||
| chr5:10598503 | A | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19830A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598503 | |||||||
| chr5:10598542 | T | C | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.367-19791T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598542 | |||||||
| chr5:10598547 | G | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19786G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598547 | |||||||
| chr5:10598552 | T | C | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19781T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598552 | |||||||
| chr5:10598571 | TTTTTG | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19746_367-1974 others(9): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10598571 | ||||||
| chr5:10598607 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.367-19726A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598607 | |||||||
| chr5:10598608 | T | A | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.367-19725T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598608 | |||||||
| chr5:10598648 | C | T | 1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.367-19685C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598648 | |||||||
| chr5:10598649 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.367-19684A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598649 | |||||||
| chr5:10598650 | G | C | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19683G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598650 | |||||||
| chr5:10598746 | T | C | 2 | a0001c0001t0001g0193 a0001c0004t0002g0256 |
2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.367-19587T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598746 | |||||||
| chr5:10598934 | T | C | 1 | a0001c0004t0014g0108 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.367-19399T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10598934 | |||||||
| chr5:10599075 | T | C | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19258T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599075 | |||||||
| chr5:10599082 | A | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19251A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599082 | |||||||
| chr5:10599214 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19119C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599214 | |||||||
| chr5:10599270 | T | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-19063T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599270 | |||||||
| chr5:10599284 | C | T | 2 | a0001c0001t0025g0319 a0001c0001t0025g0320 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.367-19049C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599284 | |||||||
| chr5:10599382 | A | G | 5 | a0001c0002t0001g0230 a0001c0006t0058g0023 a0001c0021t0011g0031 others(2): Show |
5 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-18951A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599382 | |||||||
| chr5:10599449 | G | T | 1 | a0001c0001t0047g0287 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.367-18884G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599449 | |||||||
| chr5:10599552 | A | G | 2 | a0001c0025t0019g0002 a0002c0028t0037g0007 |
2 | HG01069.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-18781A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599552 | |||||||
| chr5:10599704 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.367-18629A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599704 | |||||||
| chr5:10599739 | T | C | 1 | a0001c0001t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.367-18594T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599739 | |||||||
| chr5:10599850 | G | C | 1 | a0001c0009t0064g0085 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367-18483G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599850 | |||||||
| chr5:10599867 | T | C | 117 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.367-18466T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599867 | |||||||
| chr5:10599870 | T | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-18463T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10599870 | |||||||
| chr5:10600175 | A | G | 1 | a0001c0014t0008g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.367-18158A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10600175 | |||||||
| chr5:10600191 | G | C | 1 | a0001c0003t0003g0295 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.367-18142G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10600191 | |||||||
| chr5:10600365 | A | G | 1 | a0001c0002t0006g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.367-17968A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10600365 | |||||||
| chr5:10600408 | C | G | 1 | a0001c0002t0046g0177 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.367-17925C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10600408 | |||||||
| chr5:10600861 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-17472C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10600861 | |||||||
| chr5:10600896 | G | T | 1 | a0001c0001t0009g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.367-17437G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10600896 | |||||||
| chr5:10600957 | T | TA | 103 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0156 others(100): Show |
103 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.367-17367dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10600957 | ||||||
| chr5:10601036 | C | T | 109 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0126 others(106): Show |
109 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.367-17297C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601036 | |||||||
| chr5:10601176 | ATG | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-17154_367-1715 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10601176 | ||||||
| chr5:10601278 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.367-17055C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601278 | |||||||
| chr5:10601324 | C | T | 54 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(51): Show |
54 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.367-17009C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601324 | |||||||
| chr5:10601325 | G | A | 1 | a0001c0005t0002g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.367-17008G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601325 | |||||||
| chr5:10601348 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-16985C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601348 | |||||||
| chr5:10601445 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.367-16888C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601445 | |||||||
| chr5:10601470 | A | G | 2 | a0004c0008t0010g0323 a0004c0008t0010g0324 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.367-16863A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601470 | |||||||
| chr5:10601526 | C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367-16807C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601526 | |||||||
| chr5:10601539 | C | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-16794C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601539 | |||||||
| chr5:10601545 | G | T | 1 | a0001c0003t0017g0091 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367-16788G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601545 | |||||||
| chr5:10601562 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-16771C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601562 | |||||||
| chr5:10601726 | G | A | 1 | a0001c0013t0011g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.367-16607G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601726 | |||||||
| chr5:10601732 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-16601C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601732 | |||||||
| chr5:10601747 | T | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-16586T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601747 | |||||||
| chr5:10601938 | T | C | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.367-16395T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601938 | |||||||
| chr5:10601962 | A | G | 5 | a0001c0002t0001g0230 a0001c0006t0058g0023 a0001c0021t0011g0031 others(2): Show |
5 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-16371A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10601962 | |||||||
| chr5:10602023 | T | G | 2 | a0001c0001t0004g0081 a0001c0004t0002g0293 |
2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.367-16310T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602023 | |||||||
| chr5:10602059 | G | A | 116 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.367-16274G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602059 | |||||||
| chr5:10602117 | CTG | C | 116 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.367-16212_367-1621 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10602117 | ||||||
| chr5:10602259 | T | C | 7 | a0001c0001t0001g0308 a0001c0001t0006g0012 a0001c0001t0006g0013 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-16074T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602259 | |||||||
| chr5:10602318 | C | T | 2 | a0001c0025t0019g0002 a0002c0028t0037g0007 |
2 | HG01069.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-16015C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602318 | |||||||
| chr5:10602455 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.367-15878G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602455 | |||||||
| chr5:10602475 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.367-15858A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602475 | |||||||
| chr5:10602503 | G | C | 7 | a0001c0001t0001g0308 a0001c0001t0006g0012 a0001c0001t0006g0013 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-15830G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602503 | |||||||
| chr5:10602635 | A | G | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.367-15698A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602635 | |||||||
| chr5:10602754 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.367-15579T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602754 | |||||||
| chr5:10602808 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-15525G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602808 | |||||||
| chr5:10602815 | A | AT | 119 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(116): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.367-15503dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10602815 | ||||||
| chr5:10602815 | AT | A | 28 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(25): Show |
28 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.367-15503delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10602815 | ||||||
| chr5:10602836 | A | G | 1 | a0001c0001t0013g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.367-15497A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10602836 | |||||||
| chr5:10603003 | G | T | 7 | a0001c0001t0001g0237 a0001c0001t0001g0281 a0001c0001t0009g0034 others(4): Show |
7 | HG00280.hp1 HG01123.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.367-15330G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603003 | |||||||
| chr5:10603024 | G | A | 1 | a0001c0007t0001g0192 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.367-15309G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603024 | |||||||
| chr5:10603165 | G | A | 1 | a0001c0003t0017g0091 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367-15168G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603165 | |||||||
| chr5:10603212 | T | C | 54 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(51): Show |
54 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.367-15121T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603212 | |||||||
| chr5:10603268 | A | T | 7 | a0001c0001t0001g0308 a0001c0001t0006g0012 a0001c0001t0006g0013 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-15065A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603268 | |||||||
| chr5:10603269 | T | A | 102 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0156 others(99): Show |
102 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.367-15064T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603269 | |||||||
| chr5:10603270 | T | A | 2 | a0001c0002t0001g0216 a0001c0005t0002g0055 |
2 | HG01516.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.367-15063T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603270 | |||||||
| chr5:10603451 | C | T | 5 | a0001c0002t0001g0230 a0001c0006t0058g0023 a0001c0021t0011g0031 others(2): Show |
5 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-14882C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603451 | |||||||
| chr5:10603466 | T | A | 1 | a0001c0001t0048g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.367-14867T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603466 | |||||||
| chr5:10603765 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.367-14568G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603765 | |||||||
| chr5:10603886 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.367-14447A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10603886 | |||||||
| chr5:10603896 | C | CT | 16 | a0001c0001t0001g0066 a0001c0001t0001g0156 a0001c0001t0001g0237 others(13): Show |
16 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.367-14422dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10603896 | ||||||
| chr5:10604183 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-14150C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604183 | |||||||
| chr5:10604190 | C | CT | 173 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.367-14124dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10604190 | ||||||
| chr5:10604190 | C | CTT | 28 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0001g0237 others(25): Show |
28 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.367-14125_367-1412 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10604190 | ||||||
| chr5:10604190 | CTTTT | C | 13 | a0001c0001t0001g0076 a0001c0001t0033g0103 a0001c0001t0047g0287 others(10): Show |
13 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.367-14127_367-1412 others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10604190 | ||||||
| chr5:10604286 | G | A | 1 | a0001c0004t0040g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.367-14047G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604286 | |||||||
| chr5:10604398 | G | A | 6 | a0001c0001t0001g0126 a0001c0002t0001g0230 a0001c0006t0058g0023 others(3): Show |
6 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-13935G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604398 | |||||||
| chr5:10604514 | AAAAAAAA others(4): Show |
A | 2 | a0001c0025t0019g0002 a0002c0028t0037g0007 |
2 | HG01069.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-13802_367-1379 others(15): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10604514 | ||||||
| chr5:10604525 | G | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-13808G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604525 | |||||||
| chr5:10604526 | A | AG | 3 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-13807_367-1380 others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604526 | |||||||
| chr5:10604526 | A | G | 1 | a0007c0022t0020g0005 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.367-13807A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604526 | |||||||
| chr5:10604592 | G | A | 7 | a0001c0001t0001g0308 a0001c0001t0006g0012 a0001c0001t0006g0013 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-13741G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604592 | |||||||
| chr5:10604614 | A | C | 299 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.367-13719A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604614 | |||||||
| chr5:10604844 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.367-13489G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604844 | |||||||
| chr5:10604863 | A | G | 115 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.367-13470A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10604863 | |||||||
| chr5:10605459 | T | C | 121 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0076 others(118): Show |
121 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.367-12874T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10605459 | |||||||
| chr5:10605492 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.367-12841G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10605492 | |||||||
| chr5:10605534 | C | CT | 86 | a0001c0001t0001g0060 a0001c0001t0001g0156 a0001c0001t0001g0162 others(83): Show |
86 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.367-12788dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10605534 | ||||||
| chr5:10605560 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.367-12773T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10605560 | |||||||
| chr5:10605673 | C | T | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367-12660C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10605673 | |||||||
| chr5:10605771 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0002t0001g0140 others(3): Show |
6 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-12562C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10605771 | |||||||
| chr5:10605867 | T | C | 1 | a0001c0001t0005g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.367-12466T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10605867 | |||||||
| chr5:10606013 | T | A | 54 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(51): Show |
54 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.367-12320T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606013 | |||||||
| chr5:10606207 | T | C | 9 | a0001c0001t0001g0187 a0001c0001t0001g0310 a0001c0001t0001g0311 others(6): Show |
9 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-12126T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606207 | |||||||
| chr5:10606223 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.367-12110G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606223 | |||||||
| chr5:10606378 | C | CTT | 7 | a0001c0001t0001g0308 a0001c0001t0006g0012 a0001c0001t0006g0013 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-11955_367-1195 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606378 | |||||||
| chr5:10606453 | T | G | 113 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0076 others(110): Show |
113 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.367-11880T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606453 | |||||||
| chr5:10606463 | C | T | 1 | a0001c0013t0011g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.367-11870C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606463 | |||||||
| chr5:10606506 | T | C | 1 | a0001c0003t0003g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.367-11827T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606506 | |||||||
| chr5:10606603 | G | A | 2 | a0001c0001t0001g0290 a0001c0003t0007g0254 |
2 | NA18948.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.367-11730G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606603 | |||||||
| chr5:10606607 | G | A | 3 | a0001c0004t0002g0058 a0001c0006t0007g0059 a0002c0010t0018g0306 |
3 | HG02280.hp1 HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.367-11726G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606607 | |||||||
| chr5:10606706 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-11627C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606706 | |||||||
| chr5:10606719 | C | G | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-11614C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606719 | |||||||
| chr5:10606730 | C | CT | 20 | a0001c0001t0001g0076 a0001c0001t0001g0142 a0001c0001t0001g0271 others(17): Show |
20 | HG00741.hp1 HG01978.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.367-11587dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10606730 | ||||||
| chr5:10606811 | C | T | 1 | a0001c0006t0007g0269 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.367-11522C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606811 | |||||||
| chr5:10606863 | C | A | 2 | a0001c0001t0032g0083 a0001c0001t0032g0084 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.367-11470C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606863 | |||||||
| chr5:10606878 | G | A | 2 | a0001c0015t0004g0104 a0001c0015t0004g0105 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.367-11455G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606878 | |||||||
| chr5:10606973 | C | T | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-11360C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10606973 | |||||||
| chr5:10607265 | T | C | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-11068T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607265 | |||||||
| chr5:10607313 | C | T | 1 | a0001c0003t0003g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.367-11020C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607313 | |||||||
| chr5:10607359 | G | A | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-10974G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607359 | |||||||
| chr5:10607407 | G | A | 24 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0130 others(21): Show |
24 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.367-10926G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607407 | |||||||
| chr5:10607548 | C | T | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-10785C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607548 | |||||||
| chr5:10607638 | T | C | 1 | a0001c0002t0001g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.367-10695T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607638 | |||||||
| chr5:10607650 | C | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0004g0090 others(16): Show |
19 | HG00438.hp2 HG00738.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.367-10683C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607650 | |||||||
| chr5:10607654 | G | A | 2 | a0001c0001t0001g0300 a0001c0004t0002g0144 |
2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.367-10679G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607654 | |||||||
| chr5:10607666 | G | A | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-10667G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607666 | |||||||
| chr5:10607684 | C | T | 1 | a0001c0001t0005g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.367-10649C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607684 | |||||||
| chr5:10607685 | A | G | 295 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.367-10648A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607685 | |||||||
| chr5:10607759 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.367-10574C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607759 | |||||||
| chr5:10607954 | C | G | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-10379C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607954 | |||||||
| chr5:10607982 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.367-10351A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10607982 | |||||||
| chr5:10608154 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.367-10179G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608154 | |||||||
| chr5:10608196 | C | CA | 156 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0060 others(153): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.367-10120dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10608196 | ||||||
| chr5:10608196 | C | CAA | 13 | a0001c0001t0001g0184 a0001c0001t0001g0250 a0001c0001t0001g0268 others(10): Show |
13 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.367-10121_367-1012 others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10608196 | ||||||
| chr5:10608197 | A | C | 10 | a0001c0001t0001g0065 a0001c0001t0048g0117 a0001c0002t0001g0064 others(7): Show |
10 | HG00733.hp2 HG01258.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-10136A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608197 | |||||||
| chr5:10608356 | T | TA | 11 | a0001c0001t0001g0062 a0001c0001t0006g0220 a0001c0002t0001g0230 others(8): Show |
11 | HG00544.hp2 HG00639.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-9959dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10608356 | ||||||
| chr5:10608356 | TA | T | 6 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0002t0050g0078 others(3): Show |
6 | HG01433.hp2 HG03486.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-9959delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10608356 | ||||||
| chr5:10608405 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.367-9928A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608405 | |||||||
| chr5:10608482 | A | T | 1 | a0001c0009t0008g0289 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.367-9851A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608482 | |||||||
| chr5:10608646 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.367-9687T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608646 | |||||||
| chr5:10608662 | G | GA | 121 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0156 others(118): Show |
121 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.367-9658dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10608662 | ||||||
| chr5:10608662 | GA | G | 10 | a0001c0001t0001g0237 a0001c0001t0001g0281 a0001c0001t0001g0310 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-9658delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10608662 | ||||||
| chr5:10608786 | A | G | 1 | a0001c0009t0064g0085 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367-9547A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608786 | |||||||
| chr5:10608801 | C | T | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.367-9532C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608801 | |||||||
| chr5:10608928 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0005g0182 |
2 | NA18957.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.367-9405C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608928 | |||||||
| chr5:10608958 | C | G | 1 | a0001c0001t0052g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.367-9375C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10608958 | |||||||
| chr5:10609406 | G | A | 1 | a0001c0002t0001g0294 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.367-8927G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10609406 | |||||||
| chr5:10609430 | T | C | 1 | a0001c0003t0007g0309 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.367-8903T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10609430 | |||||||
| chr5:10609456 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.367-8877G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10609456 | |||||||
| chr5:10609721 | C | T | 4 | a0001c0001t0001g0190 a0001c0004t0002g0205 a0001c0025t0019g0002 others(1): Show |
4 | HG00099.hp2 HG01069.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-8612C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10609721 | |||||||
| chr5:10609725 | G | A | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-8608G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10609725 | |||||||
| chr5:10609778 | AGGCACCT others(17): Show |
A | 2 | a0002c0012t0034g0071 a0005c0017t0021g0127 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.367-8550_367-8527d others(26): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10609778 | ||||||
| chr5:10609960 | A | G | 1 | a0001c0003t0007g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.367-8373A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10609960 | |||||||
| chr5:10610172 | A | T | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.367-8161A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610172 | |||||||
| chr5:10610201 | C | G | 1 | a0001c0001t0065g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.367-8132C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610201 | |||||||
| chr5:10610201 | C | T | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(7): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-8132C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610201 | |||||||
| chr5:10610268 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.367-8065C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610268 | |||||||
| chr5:10610294 | G | A | 1 | a0001c0002t0016g0150 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.367-8039G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610294 | |||||||
| chr5:10610380 | G | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0168 |
2 | NA19084.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.367-7953G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610380 | |||||||
| chr5:10610412 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0240 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.367-7921G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610412 | |||||||
| chr5:10610580 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.367-7753A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610580 | |||||||
| chr5:10610659 | G | A | 114 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.367-7674G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610659 | |||||||
| chr5:10610712 | A | G | 9 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0006t0058g0023 others(6): Show |
9 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-7621A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610712 | |||||||
| chr5:10610794 | C | T | 289 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(286): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.367-7539C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610794 | |||||||
| chr5:10610837 | G | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-7496G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610837 | |||||||
| chr5:10610873 | G | A | 4 | a0001c0001t0004g0088 a0001c0004t0002g0058 a0001c0006t0007g0059 others(1): Show |
4 | HG02683.hp2 HG03491.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-7460G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610873 | |||||||
| chr5:10610902 | G | A | 4 | a0001c0001t0001g0190 a0001c0004t0002g0205 a0001c0025t0019g0002 others(1): Show |
4 | HG00099.hp2 HG01069.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-7431G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610902 | |||||||
| chr5:10610913 | G | A | 1 | a0001c0003t0007g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.367-7420G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610913 | |||||||
| chr5:10610947 | G | A | 1 | a0001c0020t0044g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.367-7386G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10610947 | |||||||
| chr5:10611022 | C | A | 17 | a0001c0001t0001g0054 a0001c0001t0001g0130 a0001c0001t0001g0244 others(14): Show |
17 | HG01106.hp1 HG02015.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.367-7311C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10611022 | |||||||
| chr5:10611240 | T | C | 10 | a0001c0001t0001g0308 a0001c0002t0001g0230 a0001c0009t0008g0304 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-7093T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10611240 | |||||||
| chr5:10611456 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0240 a0001c0002t0053g0017 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-6877C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10611456 | |||||||
| chr5:10611467 | T | C | 55 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0001t0006g0113 others(52): Show |
55 | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.367-6866T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10611467 | |||||||
| chr5:10611756 | C | T | 8 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0068 others(5): Show |
8 | HG00733.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-6577C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10611756 | |||||||
| chr5:10611778 | G | A | 16 | a0001c0001t0001g0130 a0001c0001t0001g0244 a0001c0001t0001g0248 others(13): Show |
16 | HG02015.hp1 HG02165.hp1 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.367-6555G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10611778 | |||||||
| chr5:10612174 | A | G | 6 | a0001c0001t0001g0190 a0001c0004t0002g0058 a0001c0004t0002g0205 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-6159A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612174 | |||||||
| chr5:10612202 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.367-6131C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612202 | |||||||
| chr5:10612219 | C | T | 8 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0068 others(5): Show |
8 | HG00733.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-6114C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612219 | |||||||
| chr5:10612275 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.367-6058G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612275 | |||||||
| chr5:10612291 | A | G | 4 | a0001c0001t0001g0126 a0001c0001t0006g0012 a0001c0001t0006g0013 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-6042A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612291 | |||||||
| chr5:10612381 | C | T | 1 | a0002c0012t0015g0285 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.367-5952C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612381 | |||||||
| chr5:10612515 | G | A | 195 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(192): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.367-5818G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612515 | |||||||
| chr5:10612520 | G | A | 1 | a0007c0022t0020g0005 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.367-5813G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612520 | |||||||
| chr5:10612577 | C | G | 29 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0244 others(26): Show |
29 | HG01074.hp2 HG02015.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.367-5756C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612577 | |||||||
| chr5:10612728 | A | G | 1 | a0001c0003t0060g0093 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.367-5605A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612728 | |||||||
| chr5:10612807 | A | C | 2 | a0002c0010t0018g0306 a0006c0018t0035g0112 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.367-5526A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612807 | |||||||
| chr5:10612930 | C | T | 38 | a0001c0001t0001g0305 a0001c0001t0006g0113 a0001c0001t0006g0220 others(35): Show |
38 | HG01106.hp2 HG01243.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.367-5403C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612930 | |||||||
| chr5:10612940 | C | G | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367-5393C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10612940 | |||||||
| chr5:10613194 | C | T | 2 | a0001c0009t0008g0313 a0007c0022t0020g0005 |
2 | HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.367-5139C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613194 | |||||||
| chr5:10613203 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0006g0012 a0001c0001t0006g0013 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-5130C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613203 | |||||||
| chr5:10613281 | ATTTTT | A | 283 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.367-5035_367-5031d others(7): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613281 | ||||||
| chr5:10613442 | G | T | 4 | a0001c0001t0001g0126 a0001c0001t0006g0012 a0001c0001t0006g0013 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-4891G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613442 | |||||||
| chr5:10613505 | G | C | 9 | a0001c0001t0001g0115 a0001c0001t0001g0308 a0001c0001t0029g0239 others(6): Show |
9 | HG01074.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-4828G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613505 | |||||||
| chr5:10613540 | CT | C | 39 | a0001c0001t0001g0305 a0001c0001t0006g0113 a0001c0001t0006g0220 others(36): Show |
39 | HG01106.hp2 HG01243.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.367-4787delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613540 | ||||||
| chr5:10613572 | T | G | 9 | a0001c0001t0001g0065 a0001c0001t0048g0117 a0001c0002t0001g0064 others(6): Show |
9 | HG00733.hp2 HG01258.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-4761T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613572 | |||||||
| chr5:10613712 | A | C | 1 | a0001c0001t0006g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.367-4621A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613712 | |||||||
| chr5:10613767 | G | A | 2 | a0001c0001t0001g0126 a0001c0014t0008g0125 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.367-4566G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613767 | |||||||
| chr5:10613804 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.367-4529G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10613804 | |||||||
| chr5:10613898 | CA | C | 12 | a0001c0001t0001g0065 a0001c0001t0001g0291 a0001c0002t0001g0064 others(9): Show |
12 | HG00733.hp2 HG01258.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.367-4419delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613898 | ||||||
| chr5:10613898 | CAAA | C | 39 | a0001c0001t0001g0305 a0001c0001t0006g0113 a0001c0001t0006g0220 others(36): Show |
39 | HG01106.hp2 HG01243.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.367-4421_367-4419d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613898 | ||||||
| chr5:10613990 | C | CGT | 25 | a0001c0001t0001g0129 a0001c0001t0001g0305 a0001c0001t0006g0113 others(22): Show |
25 | HG00642.hp2 HG01106.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.367-4308_367-4307d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGT | 46 | a0001c0001t0001g0043 a0001c0001t0001g0190 a0001c0001t0001g0193 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.367-4310_367-4307d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGT | 47 | a0001c0001t0001g0060 a0001c0001t0001g0180 a0001c0001t0001g0184 others(44): Show |
47 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.367-4312_367-4307d others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGTG others(1): Show |
94 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0062 others(91): Show |
94 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.367-4314_367-4307d others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGTG others(3): Show |
49 | a0001c0001t0001g0032 a0001c0001t0001g0076 a0001c0001t0001g0115 others(46): Show |
49 | HG00280.hp1 HG00408.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.367-4316_367-4307d others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGTG others(5): Show |
27 | a0001c0001t0001g0066 a0001c0001t0001g0274 a0001c0001t0001g0308 others(24): Show |
27 | HG00735.hp2 HG01074.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.367-4318_367-4307d others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGTG others(7): Show |
1 | a0001c0002t0006g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.367-4320_367-4307d others(16): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0032g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.367-4322_367-4307d others(18): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | C | CGTGTGTG others(13): Show |
1 | a0010c0029t0041g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.367-4326_367-4307d others(22): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10613990 | CGT | C | 10 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0068 others(7): Show |
10 | HG00733.hp2 HG01255.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.367-4308_367-4307d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10613990 | ||||||
| chr5:10614025 | G | A | 9 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0068 others(6): Show |
9 | HG00733.hp2 HG01255.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-4308G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614025 | |||||||
| chr5:10614025 | G | GTGTA | 6 | a0001c0002t0001g0230 a0001c0006t0058g0023 a0001c0014t0008g0128 others(3): Show |
6 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-4307_367-4306i others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10614025 | ||||||
| chr5:10614025 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0006g0012 a0001c0001t0006g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-4307_367-4306i others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10614025 | ||||||
| chr5:10614025 | G | GTGTGTGT others(11): Show |
1 | a0001c0014t0008g0125 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.367-4307_367-4306i others(20): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10614025 | ||||||
| chr5:10614025 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.367-4307_367-4306i others(22): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10614025 | ||||||
| chr5:10614034 | T | A | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367-4299T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614034 | |||||||
| chr5:10614074 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.367-4259G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614074 | |||||||
| chr5:10614226 | G | A | 291 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.367-4107G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614226 | |||||||
| chr5:10614513 | T | C | 1 | a0001c0002t0046g0177 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.367-3820T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614513 | |||||||
| chr5:10614660 | G | A | 6 | a0001c0002t0001g0230 a0001c0006t0058g0023 a0001c0014t0008g0128 others(3): Show |
6 | HG00639.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-3673G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614660 | |||||||
| chr5:10614780 | G | A | 4 | a0001c0009t0008g0313 a0004c0008t0010g0323 a0004c0008t0010g0324 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-3553G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614780 | |||||||
| chr5:10614818 | C | T | 288 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.367-3515C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614818 | |||||||
| chr5:10614892 | AC | A | 26 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0190 others(23): Show |
26 | HG00099.hp2 HG01069.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.367-3440delC | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614892 | |||||||
| chr5:10614893 | C | A | 267 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(264): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.367-3440C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614893 | |||||||
| chr5:10614978 | G | A | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367-3355G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10614978 | |||||||
| chr5:10615097 | A | G | 2 | a0001c0006t0007g0191 a0008c0036t0001g0047 |
2 | NA18950.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.367-3236A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615097 | |||||||
| chr5:10615165 | G | C | 2 | a0001c0001t0006g0012 a0001c0001t0006g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-3168G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615165 | |||||||
| chr5:10615450 | T | A | 1 | a0001c0001t0033g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.367-2883T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615450 | |||||||
| chr5:10615766 | G | A | 3 | a0001c0001t0001g0274 a0001c0001t0056g0173 a0001c0003t0003g0124 |
3 | HG00408.hp1 HG00558.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.367-2567G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615766 | |||||||
| chr5:10615792 | C | A | 1 | a0001c0003t0003g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.367-2541C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615792 | |||||||
| chr5:10615804 | A | G | 290 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.367-2529A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615804 | |||||||
| chr5:10615859 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.367-2474C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615859 | |||||||
| chr5:10615950 | T | C | 290 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.367-2383T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10615950 | |||||||
| chr5:10616019 | A | G | 1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.367-2314A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616019 | |||||||
| chr5:10616063 | A | C | 291 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.367-2270A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616063 | |||||||
| chr5:10616080 | A | G | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.367-2253A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616080 | |||||||
| chr5:10616094 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.367-2239T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616094 | |||||||
| chr5:10616218 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.367-2115G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616218 | |||||||
| chr5:10616288 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.367-2045C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616288 | |||||||
| chr5:10616304 | C | T | 1 | a0001c0001t0052g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.367-2029C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616304 | |||||||
| chr5:10616305 | G | C | 1 | a0001c0003t0003g0036 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.367-2028G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616305 | |||||||
| chr5:10616310 | T | C | 1 | a0001c0024t0011g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.367-2023T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616310 | |||||||
| chr5:10616316 | T | C | 292 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.367-2017T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616316 | |||||||
| chr5:10616325 | G | T | 1 | a0001c0015t0001g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.367-2008G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616325 | |||||||
| chr5:10616336 | G | A | 8 | a0001c0001t0001g0065 a0001c0001t0048g0117 a0001c0002t0001g0064 others(5): Show |
8 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-1997G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616336 | |||||||
| chr5:10616425 | G | A | 38 | a0001c0001t0001g0305 a0001c0001t0006g0015 a0001c0001t0006g0113 others(35): Show |
38 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.367-1908G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616425 | |||||||
| chr5:10616434 | C | G | 1 | a0001c0005t0002g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.367-1899C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616434 | |||||||
| chr5:10616455 | T | C | 3 | a0001c0009t0008g0313 a0001c0031t0062g0114 a0007c0022t0020g0005 |
3 | HG02622.hp2 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.367-1878T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616455 | |||||||
| chr5:10616467 | A | G | 291 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.367-1866A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616467 | |||||||
| chr5:10616532 | C | G | 13 | a0001c0001t0001g0190 a0001c0002t0001g0230 a0001c0004t0002g0058 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.367-1801C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616532 | |||||||
| chr5:10616564 | C | CA | 29 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0245 others(26): Show |
29 | HG00438.hp2 HG00738.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.367-1751dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10616564 | ||||||
| chr5:10616564 | C | CAAA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0187 a0001c0001t0001g0240 others(3): Show |
6 | HG01169.hp1 HG01515.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-1753_367-1751d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10616564 | ||||||
| chr5:10616564 | C | CAAAA | 181 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0060 others(178): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.367-1754_367-1751d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10616564 | ||||||
| chr5:10616564 | C | CAAAAA | 59 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0130 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.367-1755_367-1751d others(7): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10616564 | ||||||
| chr5:10616564 | C | CAAAAAA | 43 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0001t0006g0015 others(40): Show |
43 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.367-1756_367-1751d others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10616564 | ||||||
| chr5:10616654 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.367-1679G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616654 | |||||||
| chr5:10616698 | T | TTAGCTCC others(34): Show |
1 | a0001c0001t0005g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.367-1600_367-1599i others(43): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10616698 | ||||||
| chr5:10616734 | C | T | 292 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.367-1599C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616734 | |||||||
| chr5:10616778 | G | A | 293 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.367-1555G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616778 | |||||||
| chr5:10616786 | C | T | 38 | a0001c0001t0001g0305 a0001c0001t0006g0015 a0001c0001t0006g0113 others(35): Show |
38 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.367-1547C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616786 | |||||||
| chr5:10616958 | C | T | 7 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0077 others(4): Show |
7 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-1375C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10616958 | |||||||
| chr5:10617241 | T | G | 8 | a0001c0001t0001g0065 a0001c0001t0048g0117 a0001c0002t0001g0064 others(5): Show |
8 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-1092T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617241 | |||||||
| chr5:10617308 | C | T | 293 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.367-1025C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617308 | |||||||
| chr5:10617369 | G | C | 293 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.367-964G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617369 | |||||||
| chr5:10617380 | A | G | 1 | a0001c0005t0063g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367-953A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617380 | |||||||
| chr5:10617432 | G | T | 3 | a0001c0015t0001g0243 a0001c0015t0004g0104 a0001c0015t0004g0105 |
3 | HG02055.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.367-901G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617432 | |||||||
| chr5:10617450 | C | T | 1 | a0001c0001t0005g0252 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.367-883C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617450 | |||||||
| chr5:10617540 | T | C | 296 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.367-793T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617540 | |||||||
| chr5:10617558 | G | A | 276 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.367-775G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617558 | |||||||
| chr5:10617634 | AGAT | A | 11 | a0001c0001t0001g0163 a0001c0001t0001g0203 a0001c0001t0001g0211 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-695_367-693del others(3): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 10617634 | ||||||
| chr5:10617648 | C | T | 296 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.367-685C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617648 | |||||||
| chr5:10617689 | C | G | 296 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.367-644C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617689 | |||||||
| chr5:10617700 | G | A | 2 | a0001c0003t0003g0153 a0001c0007t0001g0154 |
2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.367-633G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617700 | |||||||
| chr5:10617831 | C | T | 1 | a0001c0003t0003g0036 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.367-502C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617831 | |||||||
| chr5:10617872 | G | A | 242 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.367-461G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10617872 | |||||||
| chr5:10618033 | G | A | 1 | a0001c0020t0044g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.367-300G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10618033 | |||||||
| chr5:10618072 | A | G | 1 | a0001c0002t0001g0224 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.367-261A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10618072 | |||||||
| chr5:10618145 | C | T | 28 | a0001c0001t0001g0305 a0001c0001t0006g0296 a0001c0001t0006g0297 others(25): Show |
28 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.367-188C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10618145 | |||||||
| chr5:10618239 | C | A | 7 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0077 others(4): Show |
7 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-94C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10618239 | |||||||
| chr5:10618259 | C | T | 1 | a0001c0025t0019g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.367-74C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10618259 | |||||||
| chr5:10618282 | C | G | 2 | a0001c0001t0006g0012 a0001c0001t0006g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.367-51C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 1/3 | chr5 | 10618282 | |||||||
| chr5:10618484 | T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+22T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618484 | |||||||
| chr5:10618496 | C | T | 1 | a0001c0003t0003g0036 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.496+34C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618496 | |||||||
| chr5:10618516 | C | T | 44 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0305 others(41): Show |
44 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+54C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618516 | |||||||
| chr5:10618533 | C | T | 1 | a0001c0004t0002g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.496+71C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618533 | |||||||
| chr5:10618541 | T | C | 1 | a0001c0021t0011g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.496+79T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618541 | |||||||
| chr5:10618569 | C | A | 7 | a0001c0001t0001g0065 a0001c0002t0001g0064 a0001c0002t0001g0077 others(4): Show |
7 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+107C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618569 | |||||||
| chr5:10618675 | A | T | 2 | a0001c0004t0002g0058 a0001c0006t0007g0059 |
2 | HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.496+213A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618675 | |||||||
| chr5:10618717 | C | T | 2 | a0001c0004t0002g0139 a0001c0004t0002g0141 |
2 | HG01070.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.496+255C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618717 | |||||||
| chr5:10618810 | C | T | 5 | a0001c0002t0001g0224 a0001c0003t0003g0170 a0001c0003t0003g0225 others(2): Show |
5 | HG02004.hp1 HG02132.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+348C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618810 | |||||||
| chr5:10618854 | G | T | 4 | a0001c0001t0001g0190 a0001c0004t0002g0205 a0001c0025t0019g0002 others(1): Show |
4 | HG00099.hp2 HG01069.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+392G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10618854 | |||||||
| chr5:10619147 | A | G | 1 | a0006c0018t0035g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+685A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619147 | |||||||
| chr5:10619313 | G | T | 1 | a0001c0001t0005g0118 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.496+851G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619313 | |||||||
| chr5:10619321 | G | C | 5 | a0001c0021t0011g0031 a0004c0008t0010g0323 a0004c0008t0010g0324 others(2): Show |
5 | HG02818.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+859G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619321 | |||||||
| chr5:10619378 | T | C | 20 | a0001c0001t0001g0178 a0001c0001t0001g0261 a0001c0001t0001g0271 others(17): Show |
20 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.496+916T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619378 | |||||||
| chr5:10619540 | T | A | 1 | a0001c0002t0053g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.496+1078T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619540 | |||||||
| chr5:10619646 | T | C | 1 | a0001c0002t0001g0312 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.496+1184T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619646 | |||||||
| chr5:10619788 | T | C | 1 | a0005c0017t0021g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496+1326T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619788 | |||||||
| chr5:10619841 | G | C | 127 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0129 others(124): Show |
127 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.496+1379G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619841 | |||||||
| chr5:10619936 | G | A | 3 | a0001c0001t0001g0126 a0001c0014t0008g0125 a0001c0031t0062g0114 |
3 | HG02622.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.496+1474G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619936 | |||||||
| chr5:10619943 | G | A | 105 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0129 others(102): Show |
105 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.496+1481G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619943 | |||||||
| chr5:10619973 | G | A | 102 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0129 others(99): Show |
102 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.496+1511G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10619973 | |||||||
| chr5:10620124 | C | T | 5 | a0001c0001t0012g0236 a0001c0011t0012g0003 a0002c0012t0015g0020 others(2): Show |
5 | HG01255.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+1662C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620124 | |||||||
| chr5:10620162 | C | T | 61 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0062 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.496+1700C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620162 | |||||||
| chr5:10620277 | G | A | 6 | a0001c0001t0006g0286 a0001c0002t0004g0107 a0001c0002t0027g0070 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+1815G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620277 | |||||||
| chr5:10620372 | T | C | 1 | a0001c0003t0007g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.496+1910T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620372 | |||||||
| chr5:10620403 | G | T | 1 | a0001c0001t0057g0038 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.496+1941G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620403 | |||||||
| chr5:10620480 | G | A | 1 | a0001c0001t0052g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+2018G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620480 | |||||||
| chr5:10620530 | G | A | 33 | a0001c0001t0012g0236 a0001c0002t0001g0045 a0001c0002t0001g0147 others(30): Show |
33 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.496+2068G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620530 | |||||||
| chr5:10620577 | C | T | 2 | a0001c0001t0026g0167 a0001c0001t0026g0210 |
2 | NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.496+2115C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620577 | |||||||
| chr5:10620623 | G | A | 33 | a0001c0001t0012g0236 a0001c0002t0001g0045 a0001c0002t0001g0147 others(30): Show |
33 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.496+2161G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620623 | |||||||
| chr5:10620727 | A | G | 4 | a0001c0002t0006g0322 a0005c0017t0020g0136 a0005c0017t0021g0127 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+2265A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620727 | |||||||
| chr5:10620747 | C | T | 46 | a0001c0001t0001g0032 a0001c0001t0001g0076 a0001c0001t0001g0115 others(43): Show |
46 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.496+2285C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620747 | |||||||
| chr5:10620830 | G | T | 3 | a0001c0013t0011g0030 a0001c0013t0011g0279 a0001c0024t0011g0028 |
3 | HG02723.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.496+2368G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620830 | |||||||
| chr5:10620927 | A | T | 3 | a0003c0016t0001g0006 a0003c0016t0001g0010 a0003c0035t0001g0122 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.496+2465A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10620927 | |||||||
| chr5:10621061 | G | A | 34 | a0001c0001t0012g0236 a0001c0002t0001g0045 a0001c0002t0001g0147 others(31): Show |
34 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.496+2599G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621061 | |||||||
| chr5:10621096 | C | G | 2 | a0004c0008t0010g0323 a0004c0008t0010g0324 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.496+2634C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621096 | |||||||
| chr5:10621235 | G | C | 2 | a0001c0001t0001g0211 a0001c0004t0002g0298 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.496+2773G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621235 | |||||||
| chr5:10621242 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.496+2780C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621242 | |||||||
| chr5:10621301 | A | G | 34 | a0001c0001t0012g0236 a0001c0002t0001g0045 a0001c0002t0001g0147 others(31): Show |
34 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.496+2839A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621301 | |||||||
| chr5:10621375 | A | G | 2 | a0001c0001t0001g0190 a0001c0004t0002g0205 |
2 | HG00099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.496+2913A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621375 | |||||||
| chr5:10621442 | A | C | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.496+2980A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621442 | |||||||
| chr5:10621477 | G | T | 2 | a0001c0001t0001g0211 a0001c0004t0002g0298 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.496+3015G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621477 | |||||||
| chr5:10621543 | A | G | 1 | a0001c0004t0014g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.496+3081A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621543 | |||||||
| chr5:10621604 | A | T | 1 | a0001c0001t0051g0315 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.496+3142A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621604 | |||||||
| chr5:10621743 | T | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(30): Show |
33 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.496+3281T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621743 | |||||||
| chr5:10621814 | C | A | 2 | a0001c0023t0001g0029 a0010c0029t0041g0146 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.496+3352C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621814 | |||||||
| chr5:10621936 | A | G | 33 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(30): Show |
33 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.496+3474A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10621936 | |||||||
| chr5:10622032 | A | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0138 a0001c0001t0001g0142 others(4): Show |
7 | HG00741.hp1 HG01106.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+3570A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622032 | |||||||
| chr5:10622073 | A | G | 29 | a0001c0002t0001g0045 a0001c0002t0001g0147 a0001c0002t0001g0148 others(26): Show |
29 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+3611A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622073 | |||||||
| chr5:10622228 | G | A | 1 | a0001c0025t0019g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.496+3766G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622228 | |||||||
| chr5:10622295 | C | T | 13 | a0001c0002t0001g0045 a0001c0002t0001g0157 a0001c0002t0001g0175 others(10): Show |
13 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.496+3833C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622295 | |||||||
| chr5:10622442 | CAA | C | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+3983_496+3984d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10622442 | ||||||
| chr5:10622479 | G | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(30): Show |
33 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.496+4017G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622479 | |||||||
| chr5:10622480 | C | G | 29 | a0001c0002t0001g0045 a0001c0002t0001g0147 a0001c0002t0001g0148 others(26): Show |
29 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+4018C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622480 | |||||||
| chr5:10622653 | T | A | 6 | a0001c0001t0006g0286 a0001c0002t0004g0107 a0001c0002t0027g0070 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+4191T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622653 | |||||||
| chr5:10622680 | C | T | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+4218C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622680 | |||||||
| chr5:10622689 | A | G | 18 | a0001c0002t0001g0045 a0001c0002t0001g0157 a0001c0002t0001g0175 others(15): Show |
18 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.496+4227A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622689 | |||||||
| chr5:10622717 | C | T | 1 | a0001c0001t0067g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.496+4255C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622717 | |||||||
| chr5:10622772 | C | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0301 |
2 | HG00673.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.496+4310C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622772 | |||||||
| chr5:10622794 | CTTTA | C | 39 | a0001c0001t0001g0126 a0001c0001t0001g0244 a0001c0001t0001g0248 others(36): Show |
39 | HG00609.hp2 HG01069.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.496+4336_496+4339d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10622794 | ||||||
| chr5:10622794 | CTTTAT | C | 22 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(19): Show |
22 | HG00639.hp2 HG01070.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.496+4346_496+4350d others(7): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10622794 | ||||||
| chr5:10622795 | TTTA | T | 102 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0130 others(99): Show |
102 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.496+4336_496+4338d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10622795 | ||||||
| chr5:10622796 | TTA | T | 30 | a0001c0001t0001g0274 a0001c0001t0004g0094 a0001c0001t0051g0315 others(27): Show |
30 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.496+4336_496+4337d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10622796 | ||||||
| chr5:10622797 | TA | T | 7 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4336delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622797 | |||||||
| chr5:10622803 | A | T | 201 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0115 others(198): Show |
201 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.496+4341A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622803 | |||||||
| chr5:10622806 | T | G | 7 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4344T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622806 | |||||||
| chr5:10622807 | T | G | 17 | a0001c0002t0001g0045 a0001c0002t0001g0157 a0001c0002t0001g0175 others(14): Show |
17 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.496+4345T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622807 | |||||||
| chr5:10622808 | A | G | 17 | a0001c0002t0001g0045 a0001c0002t0001g0157 a0001c0002t0001g0175 others(14): Show |
17 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.496+4346A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622808 | |||||||
| chr5:10622808 | A | T | 193 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0076 others(190): Show |
193 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.496+4346A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622808 | |||||||
| chr5:10622809 | T | A | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0003t0007g0213 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+4347T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622809 | |||||||
| chr5:10622813 | T | A | 8 | a0001c0001t0001g0054 a0001c0001t0001g0138 a0001c0001t0001g0142 others(5): Show |
8 | HG00741.hp1 HG01106.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+4351T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622813 | |||||||
| chr5:10622814 | T | A | 1 | a0001c0001t0013g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.496+4352T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622814 | |||||||
| chr5:10622957 | A | T | 2 | a0001c0006t0007g0191 a0001c0006t0007g0269 |
2 | NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.496+4495A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622957 | |||||||
| chr5:10622985 | G | A | 44 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(41): Show |
44 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+4523G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10622985 | |||||||
| chr5:10623073 | C | T | 1 | a0001c0002t0016g0150 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.496+4611C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623073 | |||||||
| chr5:10623129 | A | C | 3 | a0001c0001t0001g0228 a0001c0002t0001g0164 a0001c0002t0001g0181 |
3 | HG02074.hp2 NA18612.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.496+4667A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623129 | |||||||
| chr5:10623375 | C | A | 1 | a0001c0002t0001g0181 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.496+4913C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623375 | |||||||
| chr5:10623458 | G | A | 42 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(39): Show |
42 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.496+4996G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623458 | |||||||
| chr5:10623520 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0222 |
2 | NA18947.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.496+5058C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623520 | |||||||
| chr5:10623541 | G | C | 29 | a0001c0002t0001g0045 a0001c0002t0001g0147 a0001c0002t0001g0148 others(26): Show |
29 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+5079G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623541 | |||||||
| chr5:10623583 | G | A | 24 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0121 others(21): Show |
24 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+5121G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623583 | |||||||
| chr5:10623618 | G | A | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.496+5156G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623618 | |||||||
| chr5:10623633 | C | T | 131 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0129 others(128): Show |
131 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.496+5171C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10623633 | |||||||
| chr5:10624092 | TCTTTA | T | 100 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0130 others(97): Show |
100 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.496+5634_496+5638d others(7): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10624092 | ||||||
| chr5:10624111 | T | G | 1 | a0001c0001t0005g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.496+5649T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624111 | |||||||
| chr5:10624130 | CT | C | 28 | a0001c0001t0001g0126 a0001c0001t0001g0302 a0001c0001t0005g0052 others(25): Show |
28 | HG00639.hp1 HG01099.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.496+5685delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10624130 | ||||||
| chr5:10624135 | T | C | 9 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0003t0007g0213 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+5673T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624135 | |||||||
| chr5:10624349 | T | C | 184 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0076 others(181): Show |
184 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.496+5887T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624349 | |||||||
| chr5:10624693 | A | C | 8 | a0001c0001t0001g0126 a0001c0002t0016g0048 a0001c0002t0016g0049 others(5): Show |
8 | HG01099.hp2 HG01123.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+6231A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624693 | |||||||
| chr5:10624754 | T | G | 37 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0002t0001g0045 others(34): Show |
37 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.496+6292T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624754 | |||||||
| chr5:10624775 | T | C | 182 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0126 others(179): Show |
182 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.496+6313T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624775 | |||||||
| chr5:10624787 | G | A | 2 | a0001c0001t0001g0190 a0001c0004t0002g0205 |
2 | HG00099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.496+6325G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624787 | |||||||
| chr5:10624856 | G | T | 1 | a0001c0002t0001g0255 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.496+6394G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10624856 | |||||||
| chr5:10625003 | G | A | 7 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+6541G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625003 | |||||||
| chr5:10625041 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.496+6579G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625041 | |||||||
| chr5:10625097 | A | G | 1 | a0001c0024t0011g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.496+6635A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625097 | |||||||
| chr5:10625168 | T | C | 1 | a0001c0031t0062g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.496+6706T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625168 | |||||||
| chr5:10625182 | G | A | 10 | a0001c0001t0012g0236 a0001c0002t0004g0107 a0001c0002t0027g0070 others(7): Show |
10 | HG01255.hp1 HG01358.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.496+6720G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625182 | |||||||
| chr5:10625407 | G | A | 131 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0129 others(128): Show |
131 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.496+6945G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625407 | |||||||
| chr5:10625419 | G | A | 8 | a0001c0001t0001g0126 a0001c0002t0016g0048 a0001c0002t0016g0049 others(5): Show |
8 | HG01099.hp2 HG01123.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+6957G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625419 | |||||||
| chr5:10625512 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.496+7050C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625512 | |||||||
| chr5:10625581 | G | A | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0003t0007g0213 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+7119G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625581 | |||||||
| chr5:10625768 | G | A | 3 | a0001c0001t0042g0198 a0001c0004t0002g0139 a0001c0004t0002g0141 |
3 | HG01070.hp1 HG01167.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.496+7306G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625768 | |||||||
| chr5:10625788 | A | G | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0003t0007g0213 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+7326A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625788 | |||||||
| chr5:10625840 | C | G | 180 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0126 others(177): Show |
180 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.496+7378C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625840 | |||||||
| chr5:10625843 | C | T | 3 | a0001c0005t0002g0135 a0001c0005t0002g0174 a0001c0005t0014g0086 |
3 | HG01081.hp1 HG01358.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.496+7381C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625843 | |||||||
| chr5:10625844 | G | A | 9 | a0001c0001t0001g0126 a0001c0002t0016g0048 a0001c0002t0016g0049 others(6): Show |
9 | HG01099.hp2 HG01123.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+7382G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625844 | |||||||
| chr5:10625938 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.496+7476G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625938 | |||||||
| chr5:10625939 | A | G | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.496+7477A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10625939 | |||||||
| chr5:10626006 | G | C | 100 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0130 others(97): Show |
100 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.496+7544G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626006 | |||||||
| chr5:10626376 | C | T | 5 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(2): Show |
5 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+7914C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626376 | |||||||
| chr5:10626387 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.496+7925A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626387 | |||||||
| chr5:10626397 | T | C | 2 | a0001c0003t0007g0309 a0001c0003t0017g0080 |
2 | HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.496+7935T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626397 | |||||||
| chr5:10626537 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+8075C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626537 | |||||||
| chr5:10626645 | C | T | 178 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0126 others(175): Show |
178 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.496+8183C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626645 | |||||||
| chr5:10626655 | A | G | 1 | a0001c0004t0040g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.496+8193A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626655 | |||||||
| chr5:10626800 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.496+8338G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626800 | |||||||
| chr5:10626917 | A | C | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.496+8455A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10626917 | |||||||
| chr5:10627022 | G | A | 7 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0003t0007g0213 others(4): Show |
7 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+8560G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627022 | |||||||
| chr5:10627166 | C | T | 1 | a0003c0019t0028g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.496+8704C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627166 | |||||||
| chr5:10627337 | G | A | 99 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0130 others(96): Show |
99 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.496+8875G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627337 | |||||||
| chr5:10627400 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.496+8938A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627400 | |||||||
| chr5:10627494 | G | A | 1 | a0010c0029t0041g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.496+9032G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627494 | |||||||
| chr5:10627499 | CG | C | 5 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(2): Show |
5 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+9041delG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10627499 | ||||||
| chr5:10627504 | A | T | 5 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(2): Show |
5 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+9042A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627504 | |||||||
| chr5:10627553 | G | A | 1 | a0001c0005t0002g0174 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.496+9091G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627553 | |||||||
| chr5:10627957 | G | T | 1 | a0001c0001t0068g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.496+9495G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10627957 | |||||||
| chr5:10628017 | C | T | 1 | a0001c0005t0014g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.496+9555C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628017 | |||||||
| chr5:10628036 | C | T | 5 | a0001c0001t0006g0296 a0001c0001t0006g0297 a0001c0014t0008g0018 others(2): Show |
5 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+9574C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628036 | |||||||
| chr5:10628093 | T | C | 24 | a0001c0001t0001g0244 a0001c0001t0005g0050 a0001c0001t0005g0052 others(21): Show |
24 | HG00609.hp2 HG01978.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+9631T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628093 | |||||||
| chr5:10628122 | C | T | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.496+9660C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628122 | |||||||
| chr5:10628123 | A | G | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.496+9661A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628123 | |||||||
| chr5:10628243 | T | C | 1 | a0001c0001t0033g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.496+9781T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628243 | |||||||
| chr5:10628273 | C | T | 1 | a0001c0014t0008g0125 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497-9755C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628273 | |||||||
| chr5:10628274 | G | A | 2 | a0001c0001t0001g0305 a0001c0011t0001g0001 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.497-9754G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628274 | |||||||
| chr5:10628859 | C | A | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.497-9169C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628859 | |||||||
| chr5:10628880 | C | T | 1 | a0001c0002t0027g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.497-9148C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628880 | |||||||
| chr5:10628962 | G | A | 6 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-9066G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10628962 | |||||||
| chr5:10629160 | G | A | 2 | a0001c0005t0002g0067 a0001c0006t0007g0191 |
2 | HG01258.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.497-8868G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629160 | |||||||
| chr5:10629339 | G | C | 124 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0130 others(121): Show |
124 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.497-8689G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629339 | |||||||
| chr5:10629352 | G | A | 1 | a0001c0001t0004g0092 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.497-8676G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629352 | |||||||
| chr5:10629475 | T | G | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-8553T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629475 | |||||||
| chr5:10629524 | G | A | 1 | a0001c0001t0052g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-8504G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629524 | |||||||
| chr5:10629601 | G | A | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.497-8427G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629601 | |||||||
| chr5:10629779 | G | C | 2 | a0005c0017t0020g0136 a0007c0022t0020g0005 |
2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497-8249G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10629779 | |||||||
| chr5:10630059 | C | CA | 97 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0001t0005g0229 others(94): Show |
97 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.497-7969_497-7968i others(3): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630059 | |||||||
| chr5:10630086 | A | G | 97 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0001t0005g0229 others(94): Show |
97 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.497-7942A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630086 | |||||||
| chr5:10630112 | G | A | 2 | a0003c0019t0028g0011 a0003c0019t0028g0232 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.497-7916G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630112 | |||||||
| chr5:10630208 | T | C | 135 | a0001c0001t0001g0076 a0001c0001t0001g0130 a0001c0001t0001g0228 others(132): Show |
135 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.497-7820T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630208 | |||||||
| chr5:10630437 | G | T | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-7591G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630437 | |||||||
| chr5:10630440 | C | T | 1 | a0001c0001t0056g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.497-7588C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630440 | |||||||
| chr5:10630522 | A | G | 11 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-7506A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630522 | |||||||
| chr5:10630547 | A | G | 40 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0002t0001g0045 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.497-7481A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630547 | |||||||
| chr5:10630614 | A | G | 3 | a0001c0001t0005g0252 a0006c0018t0035g0112 a0006c0018t0061g0087 |
3 | HG02071.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.497-7414A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630614 | |||||||
| chr5:10630736 | G | A | 3 | a0001c0002t0006g0322 a0005c0017t0020g0136 a0007c0022t0020g0005 |
3 | HG02895.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497-7292G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630736 | |||||||
| chr5:10630805 | T | G | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-7223T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630805 | |||||||
| chr5:10630825 | G | A | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-7203G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630825 | |||||||
| chr5:10630828 | G | A | 1 | a0001c0002t0001g0226 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.497-7200G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630828 | |||||||
| chr5:10630868 | G | A | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-7160G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630868 | |||||||
| chr5:10630870 | C | CA | 15 | a0001c0001t0001g0076 a0001c0001t0001g0129 a0001c0001t0001g0291 others(12): Show |
15 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-7142dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10630870 | ||||||
| chr5:10630870 | C | CAA | 19 | a0001c0002t0001g0045 a0001c0002t0001g0068 a0001c0002t0001g0147 others(16): Show |
19 | HG00140.hp1 HG00673.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.497-7143_497-7142d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10630870 | ||||||
| chr5:10630870 | C | CAAA | 68 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(65): Show |
68 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.497-7144_497-7142d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10630870 | ||||||
| chr5:10630870 | C | CAAAA | 17 | a0001c0002t0001g0265 a0001c0002t0001g0294 a0001c0002t0030g0039 others(14): Show |
17 | HG01074.hp1 HG02165.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-7145_497-7142d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10630870 | ||||||
| chr5:10630875 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.497-7153A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10630875 | |||||||
| chr5:10630884 | A | AAAG | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-7135_497-7133d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10630884 | ||||||
| chr5:10631013 | A | G | 96 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0001t0005g0229 others(93): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.497-7015A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631013 | |||||||
| chr5:10631025 | A | G | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-7003A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631025 | |||||||
| chr5:10631035 | G | A | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-6993G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631035 | |||||||
| chr5:10631066 | T | C | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-6962T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631066 | |||||||
| chr5:10631107 | C | T | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-6921C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631107 | |||||||
| chr5:10631172 | C | G | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-6856C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631172 | |||||||
| chr5:10631319 | T | C | 95 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0002t0001g0040 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.497-6709T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631319 | |||||||
| chr5:10631366 | A | G | 7 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-6662A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631366 | |||||||
| chr5:10631370 | G | C | 2 | a0003c0019t0028g0011 a0003c0019t0028g0232 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.497-6658G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631370 | |||||||
| chr5:10631379 | C | T | 1 | a0001c0004t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.497-6649C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631379 | |||||||
| chr5:10631443 | A | G | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-6585A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631443 | |||||||
| chr5:10631696 | A | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-6332A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631696 | |||||||
| chr5:10631725 | T | A | 2 | a0001c0003t0022g0041 a0001c0003t0022g0119 |
2 | NA18975.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.497-6303T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631725 | |||||||
| chr5:10631769 | G | A | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-6259G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631769 | |||||||
| chr5:10631853 | G | A | 11 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-6175G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631853 | |||||||
| chr5:10631860 | A | G | 94 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0063 others(91): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.497-6168A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10631860 | |||||||
| chr5:10632049 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5979T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632049 | |||||||
| chr5:10632075 | G | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0257 a0001c0001t0001g0310 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-5953G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632075 | |||||||
| chr5:10632143 | C | T | 2 | a0001c0002t0001g0040 a0001c0002t0001g0172 |
2 | NA18952.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.497-5885C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632143 | |||||||
| chr5:10632248 | A | G | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5780A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632248 | |||||||
| chr5:10632313 | A | G | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5715A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632313 | |||||||
| chr5:10632320 | A | G | 70 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0063 others(67): Show |
70 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.497-5708A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632320 | |||||||
| chr5:10632391 | C | T | 27 | a0001c0002t0001g0045 a0001c0002t0001g0147 a0001c0002t0001g0148 others(24): Show |
27 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-5637C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632391 | |||||||
| chr5:10632409 | G | A | 16 | a0001c0002t0046g0177 a0001c0003t0003g0036 a0001c0003t0003g0262 others(13): Show |
16 | HG01074.hp1 HG01978.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-5619G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632409 | |||||||
| chr5:10632425 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5603T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632425 | |||||||
| chr5:10632479 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5549T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632479 | |||||||
| chr5:10632493 | G | C | 25 | a0001c0002t0001g0045 a0001c0002t0001g0147 a0001c0002t0001g0148 others(22): Show |
25 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.497-5535G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632493 | |||||||
| chr5:10632518 | A | G | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.497-5510A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632518 | |||||||
| chr5:10632522 | C | A | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.497-5506C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632522 | |||||||
| chr5:10632532 | T | A | 3 | a0001c0002t0001g0149 a0001c0002t0001g0183 a0001c0005t0002g0272 |
3 | HG00558.hp2 HG02080.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.497-5496T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632532 | |||||||
| chr5:10632558 | G | C | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.497-5470G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632558 | |||||||
| chr5:10632631 | C | T | 119 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-5397C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632631 | |||||||
| chr5:10632637 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5391T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632637 | |||||||
| chr5:10632757 | A | G | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5271A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632757 | |||||||
| chr5:10632816 | C | T | 27 | a0001c0002t0001g0045 a0001c0002t0001g0147 a0001c0002t0001g0148 others(24): Show |
27 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-5212C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632816 | |||||||
| chr5:10632842 | C | T | 1 | a0001c0003t0003g0053 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.497-5186C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632842 | |||||||
| chr5:10632913 | G | A | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5115G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632913 | |||||||
| chr5:10632986 | C | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-5042C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632986 | |||||||
| chr5:10632988 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0168 |
2 | NA19084.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.497-5040A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10632988 | |||||||
| chr5:10633051 | G | T | 1 | a0001c0003t0007g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.497-4977G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633051 | |||||||
| chr5:10633097 | CT | C | 7 | a0001c0001t0001g0166 a0001c0001t0001g0248 a0001c0001t0013g0196 others(4): Show |
7 | HG01169.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-4914delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10633097 | ||||||
| chr5:10633107 | TTTTTTTT others(1): Show |
T | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-4915_497-4908d others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10633107 | ||||||
| chr5:10633108 | TTTTTTTC | T | 114 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(111): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.497-4914_497-4908d others(9): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10633108 | ||||||
| chr5:10633225 | C | T | 88 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0063 others(85): Show |
88 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.497-4803C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633225 | |||||||
| chr5:10633385 | C | T | 99 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(96): Show |
99 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.497-4643C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633385 | |||||||
| chr5:10633424 | TTTTGA | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-4598_497-4594d others(7): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10633424 | ||||||
| chr5:10633447 | T | C | 132 | a0001c0001t0001g0076 a0001c0001t0001g0130 a0001c0001t0006g0024 others(129): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.497-4581T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633447 | |||||||
| chr5:10633490 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0024g0206 a0001c0001t0031g0082 others(1): Show |
4 | HG02056.hp1 NA18969.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-4538C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633490 | |||||||
| chr5:10633555 | C | G | 1 | a0001c0002t0001g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.497-4473C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633555 | |||||||
| chr5:10633809 | C | A | 10 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0003c0016t0001g0006 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-4219C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633809 | |||||||
| chr5:10633817 | A | G | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-4211A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633817 | |||||||
| chr5:10633836 | C | T | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.497-4192C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633836 | |||||||
| chr5:10633918 | C | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-4110C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633918 | |||||||
| chr5:10633963 | G | A | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-4065G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633963 | |||||||
| chr5:10633970 | G | A | 2 | a0002c0012t0015g0020 a0002c0012t0015g0285 |
2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.497-4058G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10633970 | |||||||
| chr5:10634095 | A | G | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-3933A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634095 | |||||||
| chr5:10634138 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.497-3890A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634138 | |||||||
| chr5:10634143 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.497-3885T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634143 | |||||||
| chr5:10634170 | C | T | 69 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0063 others(66): Show |
69 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.497-3858C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634170 | |||||||
| chr5:10634255 | T | C | 1 | a0010c0029t0041g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.497-3773T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634255 | |||||||
| chr5:10634292 | C | G | 3 | a0001c0002t0016g0048 a0001c0002t0016g0049 a0001c0002t0016g0150 |
3 | HG01099.hp2 HG01123.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.497-3736C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634292 | |||||||
| chr5:10634350 | TGTTCTGG others(1): Show |
T | 124 | a0001c0001t0001g0065 a0001c0001t0001g0130 a0001c0002t0001g0040 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.497-3672_497-3665d others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634350 | ||||||
| chr5:10634374 | C | G | 1 | a0001c0002t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.497-3654C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634374 | |||||||
| chr5:10634457 | A | AT | 12 | a0001c0002t0001g0045 a0001c0002t0001g0175 a0001c0002t0001g0230 others(9): Show |
12 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-3564dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634457 | ||||||
| chr5:10634457 | A | ATT | 83 | a0001c0002t0001g0040 a0001c0002t0001g0063 a0001c0002t0001g0064 others(80): Show |
83 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.497-3565_497-3564d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634457 | ||||||
| chr5:10634457 | A | ATTT | 13 | a0001c0001t0001g0130 a0001c0002t0001g0137 a0001c0002t0001g0278 others(10): Show |
13 | HG00408.hp1 HG00639.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.497-3566_497-3564d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634457 | ||||||
| chr5:10634457 | A | ATTTT | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00738.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-3567_497-3564d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634457 | ||||||
| chr5:10634465 | C | T | 117 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(114): Show |
117 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.497-3563C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634465 | |||||||
| chr5:10634495 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0240 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.497-3533T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634495 | |||||||
| chr5:10634522 | T | A | 1 | a0001c0001t0006g0286 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.497-3506T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634522 | |||||||
| chr5:10634528 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-3500T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634528 | |||||||
| chr5:10634573 | C | T | 3 | a0001c0003t0007g0259 a0001c0003t0017g0091 a0001c0003t0017g0095 |
3 | NA18959.hp2 NA18973.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.497-3455C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634573 | |||||||
| chr5:10634675 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-3353T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634675 | |||||||
| chr5:10634705 | C | T | 10 | a0001c0001t0001g0130 a0001c0002t0001g0064 a0001c0002t0001g0140 others(7): Show |
10 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-3323C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634705 | |||||||
| chr5:10634748 | A | G | 1 | a0008c0036t0001g0047 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.497-3280A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634748 | |||||||
| chr5:10634778 | G | A | 16 | a0001c0002t0046g0177 a0001c0003t0003g0036 a0001c0003t0003g0262 others(13): Show |
16 | HG01074.hp1 HG01978.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-3250G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634778 | |||||||
| chr5:10634807 | G | T | 15 | a0001c0003t0003g0036 a0001c0003t0003g0262 a0001c0003t0007g0215 others(12): Show |
15 | HG01074.hp1 HG01978.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-3221G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634807 | |||||||
| chr5:10634856 | C | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-3172C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634856 | |||||||
| chr5:10634868 | T | TAAAGAAG others(309): Show |
1 | a0001c0002t0001g0045 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.497-3146_497-3145i others(318): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(310): Show |
96 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0063 others(93): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.497-3146_497-3145i others(319): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(311): Show |
1 | a0001c0002t0001g0151 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.497-3146_497-3145i others(320): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(312): Show |
5 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0304 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-3146_497-3145i others(321): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(313): Show |
4 | a0001c0009t0008g0289 a0003c0019t0028g0011 a0003c0019t0028g0232 others(1): Show |
4 | HG01361.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-3146_497-3145i others(322): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(314): Show |
11 | a0001c0002t0001g0137 a0001c0002t0001g0147 a0001c0002t0001g0148 others(8): Show |
11 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-3146_497-3145i others(323): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(314): Show |
2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.497-3146_497-3145i others(323): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634868 | T | TAAAGAAG others(310): Show |
1 | a0001c0002t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-3146_497-3145i others(319): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10634868 | ||||||
| chr5:10634998 | C | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-3030C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10634998 | |||||||
| chr5:10635126 | G | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-2902G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635126 | |||||||
| chr5:10635202 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.497-2826C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635202 | |||||||
| chr5:10635232 | G | A | 12 | a0001c0002t0001g0045 a0001c0002t0001g0157 a0001c0002t0001g0175 others(9): Show |
12 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-2796G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635232 | |||||||
| chr5:10635250 | A | G | 7 | a0001c0001t0001g0258 a0001c0002t0004g0107 a0001c0002t0027g0070 others(4): Show |
7 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-2778A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635250 | |||||||
| chr5:10635255 | T | C | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-2773T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635255 | |||||||
| chr5:10635364 | T | C | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-2664T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635364 | |||||||
| chr5:10635412 | C | G | 1 | a0001c0004t0002g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.497-2616C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635412 | |||||||
| chr5:10635417 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.497-2611C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635417 | |||||||
| chr5:10635471 | A | T | 1 | a0001c0025t0019g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497-2557A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635471 | |||||||
| chr5:10635633 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.497-2395C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635633 | |||||||
| chr5:10635780 | C | G | 1 | a0002c0012t0034g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.497-2248C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635780 | |||||||
| chr5:10635835 | C | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-2193C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635835 | |||||||
| chr5:10635865 | G | GA | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-2161dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10635865 | ||||||
| chr5:10635955 | G | A | 122 | a0001c0001t0001g0130 a0001c0001t0001g0248 a0001c0002t0001g0040 others(119): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.497-2073G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635955 | |||||||
| chr5:10635965 | C | T | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-2063C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635965 | |||||||
| chr5:10635966 | G | C | 1 | a0001c0006t0058g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.497-2062G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10635966 | |||||||
| chr5:10636039 | G | A | 105 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0063 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.497-1989G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636039 | |||||||
| chr5:10636052 | C | T | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-1976C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636052 | |||||||
| chr5:10636124 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.497-1904A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636124 | |||||||
| chr5:10636127 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.497-1901C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636127 | |||||||
| chr5:10636142 | G | A | 122 | a0001c0001t0001g0130 a0001c0001t0001g0268 a0001c0002t0001g0040 others(119): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.497-1886G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636142 | |||||||
| chr5:10636170 | GGGGA | G | 121 | a0001c0001t0001g0130 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-1851_497-1848d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10636170 | ||||||
| chr5:10636212 | A | T | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.497-1816A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636212 | |||||||
| chr5:10636236 | C | T | 4 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-1792C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636236 | |||||||
| chr5:10636265 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.497-1763G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636265 | |||||||
| chr5:10636283 | G | C | 1 | a0001c0001t0005g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.497-1745G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636283 | |||||||
| chr5:10636298 | C | T | 6 | a0001c0002t0001g0247 a0001c0002t0004g0096 a0001c0002t0004g0097 others(3): Show |
6 | NA18964.hp2 NA18967.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-1730C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636298 | |||||||
| chr5:10636301 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0228 a0001c0002t0006g0322 others(3): Show |
6 | HG02074.hp1 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-1727C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636301 | |||||||
| chr5:10636310 | T | C | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-1718T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636310 | |||||||
| chr5:10636381 | G | A | 13 | a0001c0002t0001g0045 a0001c0002t0001g0157 a0001c0002t0001g0175 others(10): Show |
13 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.497-1647G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636381 | |||||||
| chr5:10636457 | A | AT | 120 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(117): Show |
120 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.497-1563dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10636457 | ||||||
| chr5:10636457 | A | T | 1 | a0001c0001t0004g0088 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.497-1571A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636457 | |||||||
| chr5:10636481 | A | G | 1 | a0001c0002t0053g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-1547A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636481 | |||||||
| chr5:10636571 | C | T | 18 | a0001c0002t0001g0176 a0001c0002t0001g0275 a0001c0002t0001g0278 others(15): Show |
18 | HG00408.hp1 HG00544.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-1457C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636571 | |||||||
| chr5:10636826 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-1202G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636826 | |||||||
| chr5:10636850 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-1178C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636850 | |||||||
| chr5:10636929 | G | C | 1 | a0001c0003t0007g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.497-1099G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10636929 | |||||||
| chr5:10637041 | G | A | 3 | a0001c0013t0011g0030 a0001c0013t0011g0279 a0001c0024t0011g0028 |
3 | HG02723.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.497-987G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637041 | |||||||
| chr5:10637064 | C | T | 1 | a0001c0001t0013g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.497-964C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637064 | |||||||
| chr5:10637104 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-924T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637104 | |||||||
| chr5:10637218 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.497-810T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637218 | |||||||
| chr5:10637413 | C | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-615C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637413 | |||||||
| chr5:10637425 | G | GAC | 10 | a0001c0001t0001g0062 a0001c0001t0001g0142 a0001c0001t0006g0283 others(7): Show |
10 | HG00639.hp2 HG00741.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-566_497-565dup others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACAC | 11 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0004g0088 others(8): Show |
11 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-568_497-565dup others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACAC | 40 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0131 others(37): Show |
40 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.497-570_497-565dup others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(1): Show |
35 | a0001c0001t0001g0043 a0001c0001t0001g0121 a0001c0001t0001g0126 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.497-572_497-565dup others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(3): Show |
42 | a0001c0001t0001g0249 a0001c0001t0027g0133 a0001c0001t0029g0239 others(39): Show |
42 | HG00544.hp1 HG00639.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.497-574_497-565dup others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(5): Show |
20 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0001c0001t0001g0242 others(17): Show |
20 | HG00597.hp2 HG01069.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.497-576_497-565dup others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(7): Show |
15 | a0001c0001t0001g0268 a0001c0001t0001g0290 a0001c0002t0001g0072 others(12): Show |
15 | HG00741.hp2 HG01515.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-578_497-565dup others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(9): Show |
6 | a0001c0001t0001g0248 a0001c0001t0042g0198 a0001c0003t0007g0213 others(3): Show |
6 | HG02602.hp1 HG02622.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-580_497-565dup others(16): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(11): Show |
2 | a0001c0005t0002g0061 a0005c0017t0020g0136 |
2 | HG03239.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497-582_497-565dup others(18): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(13): Show |
1 | a0001c0002t0006g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.497-584_497-565dup others(20): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GACACACA others(15): Show |
2 | a0005c0017t0021g0127 a0007c0022t0020g0005 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.497-586_497-565dup others(22): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GAGACACA others(3): Show |
1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.497-602_497-601ins others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GAGACACA others(5): Show |
2 | a0003c0016t0001g0006 a0003c0016t0001g0010 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.497-602_497-601ins others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | G | GAGACACA others(7): Show |
1 | a0003c0035t0001g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.497-602_497-601ins others(14): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | GAC | G | 47 | a0001c0001t0001g0060 a0001c0001t0001g0130 a0001c0001t0001g0166 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.497-566_497-565del others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | GACAC | G | 16 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0156 others(13): Show |
16 | HG00099.hp2 HG00733.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-568_497-565del others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | GACACAC | G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0211 a0001c0001t0001g0218 others(1): Show |
4 | HG00673.hp1 HG01175.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-570_497-565del others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0244 a0001c0001t0005g0052 a0001c0001t0005g0165 |
3 | HG02015.hp1 NA18747.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.497-572_497-565del others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637425 | GACACACA others(3): Show |
G | 5 | a0001c0001t0005g0050 a0001c0001t0005g0169 a0001c0001t0005g0235 others(2): Show |
5 | HG00609.hp2 NA18612.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-574_497-565del others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637425 | ||||||
| chr5:10637427 | C | G | 7 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-601C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637427 | |||||||
| chr5:10637462 | A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0076 a0001c0001t0006g0024 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.497-565_497-564ins others(13): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637462 | ||||||
| chr5:10637462 | A | ACACACAC others(4): Show |
4 | a0004c0008t0010g0075 a0004c0008t0010g0292 a0004c0008t0010g0323 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-565_497-564ins others(11): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637462 | ||||||
| chr5:10637464 | G | C | 1 | a0001c0005t0002g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.497-564G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637464 | |||||||
| chr5:10637465 | G | A | 3 | a0001c0005t0002g0299 a0006c0018t0035g0112 a0006c0018t0061g0087 |
3 | HG02965.hp2 HG03139.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.497-563G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637465 | |||||||
| chr5:10637472 | G | C | 3 | a0001c0005t0002g0299 a0006c0018t0035g0112 a0006c0018t0061g0087 |
3 | HG02965.hp2 HG03139.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.497-556G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637472 | |||||||
| chr5:10637473 | G | A | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-555G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637473 | |||||||
| chr5:10637494 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.497-534G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637494 | |||||||
| chr5:10637529 | C | CAG | 121 | a0001c0001t0033g0103 a0001c0002t0001g0040 a0001c0002t0001g0045 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.497-498_497-497dup others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 10637529 | ||||||
| chr5:10637685 | T | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-343T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637685 | |||||||
| chr5:10637759 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-269A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637759 | |||||||
| chr5:10637836 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-192C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637836 | |||||||
| chr5:10637855 | C | T | 3 | a0001c0001t0027g0133 a0001c0001t0032g0083 a0001c0001t0032g0084 |
3 | HG02809.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.497-173C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 2/3 | chr5 | 10637855 | |||||||
| chr5:10638213 | C | T | 2 | a0003c0019t0028g0011 a0003c0019t0028g0232 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.637+45C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638213 | |||||||
| chr5:10638252 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+84A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638252 | |||||||
| chr5:10638279 | T | C | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.637+111T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638279 | |||||||
| chr5:10638425 | T | G | 3 | a0001c0002t0001g0063 a0001c0002t0001g0077 a0001c0002t0001g0255 |
3 | HG02602.hp2 HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.637+257T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638425 | |||||||
| chr5:10638442 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+274G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638442 | |||||||
| chr5:10638513 | A | C | 3 | a0001c0013t0011g0030 a0001c0013t0011g0279 a0001c0024t0011g0028 |
3 | HG02723.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.637+345A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638513 | |||||||
| chr5:10638526 | G | T | 3 | a0001c0001t0012g0016 a0001c0001t0012g0019 a0001c0001t0047g0287 |
3 | HG01243.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.637+358G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638526 | |||||||
| chr5:10638576 | G | A | 4 | a0001c0002t0006g0322 a0005c0017t0020g0136 a0005c0017t0021g0127 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+408G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638576 | |||||||
| chr5:10638699 | G | A | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.637+531G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638699 | |||||||
| chr5:10638726 | C | T | 97 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(94): Show |
97 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.637+558C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638726 | |||||||
| chr5:10638757 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+589C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638757 | |||||||
| chr5:10638768 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+600G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638768 | |||||||
| chr5:10638779 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+611C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638779 | |||||||
| chr5:10638878 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+710T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638878 | |||||||
| chr5:10638884 | C | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+716C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638884 | |||||||
| chr5:10638885 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+717G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638885 | |||||||
| chr5:10638901 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+733T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638901 | |||||||
| chr5:10638903 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+735T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638903 | |||||||
| chr5:10638906 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+738T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638906 | |||||||
| chr5:10638922 | C | T | 3 | a0001c0001t0006g0296 a0001c0001t0006g0297 a0001c0004t0002g0207 |
3 | HG02735.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.637+754C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638922 | |||||||
| chr5:10638938 | GATATTAG others(1140): Show |
G | 112 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.637+773_637+1919de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638938 | ||||||
| chr5:10638941 | A | G | 7 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+773A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638941 | |||||||
| chr5:10638941 | ATTAGCGG others(24): Show |
A | 1 | a0001c0004t0014g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+796_637+826del others(31): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638941 | ||||||
| chr5:10638947 | GGGTGACG others(55): Show |
G | 1 | a0001c0001t0032g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.637+796_637+857del others(62): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638947 | ||||||
| chr5:10638958 | AGTTGCAC others(1128): Show |
A | 1 | a0001c0003t0007g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.637+792_637+1926de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638958 | ||||||
| chr5:10638964 | A | G | 8 | a0001c0001t0001g0305 a0001c0002t0001g0147 a0001c0002t0001g0148 others(5): Show |
8 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+796A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638964 | |||||||
| chr5:10638964 | ACGGCGAT others(24): Show |
A | 3 | a0001c0001t0042g0198 a0001c0004t0002g0139 a0001c0004t0002g0141 |
3 | HG01070.hp1 HG01167.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.637+809_637+839del others(31): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638964 | ||||||
| chr5:10638964 | ACGGCGAT others(86): Show |
A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0142 a0001c0001t0001g0300 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+914_637+1006de others(94): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638964 | ||||||
| chr5:10638964 | ACGGCGAT others(210): Show |
A | 7 | a0001c0006t0007g0191 a0001c0006t0007g0269 a0001c0014t0008g0018 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.637+809_637+1025de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638964 | ||||||
| chr5:10638968 | C | T | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+800C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638968 | |||||||
| chr5:10638976 | GCGGGTGA others(54): Show |
G | 16 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0131 others(13): Show |
16 | HG01069.hp1 HG01515.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+809_637+869del others(61): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638976 | |||||||
| chr5:10638976 | GCGGGTGA others(302): Show |
G | 40 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0126 others(37): Show |
40 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.637+809_637+1117de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638976 | |||||||
| chr5:10638977 | C | G | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+809C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638977 | |||||||
| chr5:10638977 | C | T | 1 | a0001c0001t0005g0185 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.637+809C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638977 | |||||||
| chr5:10638978 | G | C | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+810G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638978 | |||||||
| chr5:10638978 | GGGTGACG others(365): Show |
G | 1 | a0001c0001t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.637+840_637+1211de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638978 | ||||||
| chr5:10638985 | G | A | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+817G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638985 | |||||||
| chr5:10638986 | C | CGGAGTTG others(210): Show |
1 | a0001c0004t0040g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.637+840_637+1056du others(218): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638986 | ||||||
| chr5:10638986 | C | T | 1 | a0001c0004t0014g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+818C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638986 | |||||||
| chr5:10638989 | A | G | 1 | a0001c0004t0014g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+821A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10638989 | |||||||
| chr5:10638989 | AGTTGCGC others(334): Show |
A | 1 | a0001c0001t0055g0116 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.637+914_637+1254de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638989 | ||||||
| chr5:10638999 | CGATGTTA others(1109): Show |
C | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+840_637+1955de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10638999 | ||||||
| chr5:10639008 | G | C | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+840G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639008 | |||||||
| chr5:10639009 | C | G | 8 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+841C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639009 | |||||||
| chr5:10639009 | CGGTGACG others(55): Show |
C | 5 | a0001c0001t0001g0218 a0001c0001t0001g0274 a0001c0001t0001g0301 others(2): Show |
5 | HG00673.hp1 HG02027.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+871_637+932del others(62): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639009 | ||||||
| chr5:10639016 | G | A | 3 | a0001c0001t0042g0198 a0001c0004t0002g0139 a0001c0004t0002g0141 |
3 | HG01070.hp1 HG01167.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.637+848G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639016 | |||||||
| chr5:10639037 | A | G | 1 | a0001c0006t0003g0267 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.637+869A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639037 | |||||||
| chr5:10639039 | C | G | 9 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0001t0032g0084 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+871C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639039 | |||||||
| chr5:10639039 | CG | C | 16 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0131 others(13): Show |
16 | HG01069.hp1 HG01515.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+874delG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639039 | ||||||
| chr5:10639040 | G | C | 9 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0001t0032g0084 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+872G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639040 | |||||||
| chr5:10639040 | GGGTGACG others(396): Show |
G | 1 | a0001c0001t0001g0271 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.637+933_637+1335de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639040 | ||||||
| chr5:10639047 | G | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0131 others(17): Show |
20 | HG00609.hp1 HG01069.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+879G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639047 | |||||||
| chr5:10639048 | CGGAGTTG others(210): Show |
C | 2 | a0001c0001t0001g0190 a0001c0004t0002g0205 |
2 | HG00099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.637+933_637+1149de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639048 | ||||||
| chr5:10639051 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.637+883A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639051 | |||||||
| chr5:10639070 | C | G | 4 | a0001c0001t0001g0130 a0001c0001t0042g0198 a0001c0004t0002g0139 others(1): Show |
4 | HG01070.hp1 HG01167.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+902C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639070 | |||||||
| chr5:10639071 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0042g0198 a0001c0004t0002g0139 others(1): Show |
4 | HG01070.hp1 HG01167.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+903G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639071 | |||||||
| chr5:10639071 | GGGTGACG others(24): Show |
G | 1 | a0001c0001t0004g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637+933_637+963del others(31): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639071 | ||||||
| chr5:10639071 | GGGTGACG others(613): Show |
G | 7 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+933_637+1552de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639071 | ||||||
| chr5:10639079 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.637+911C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639079 | |||||||
| chr5:10639079 | CGGAGTTG others(179): Show |
C | 1 | a0001c0001t0065g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.637+933_637+1118de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639079 | ||||||
| chr5:10639082 | A | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0234 a0001c0001t0001g0261 others(1): Show |
4 | HG00597.hp1 HG01109.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+914A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639082 | |||||||
| chr5:10639082 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.637+914A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639082 | |||||||
| chr5:10639082 | AGTTGCGC others(241): Show |
A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0240 a0001c0001t0012g0019 |
3 | HG02280.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.637+1007_637+1254d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639082 | ||||||
| chr5:10639082 | AGTTGCGC others(582): Show |
A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0277 a0001c0004t0002g0042 others(1): Show |
4 | HG00733.hp1 HG01361.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1004_637+1592d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639082 | ||||||
| chr5:10639101 | G | C | 6 | a0001c0001t0042g0198 a0001c0004t0002g0139 a0001c0004t0002g0141 others(3): Show |
6 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+933G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639101 | |||||||
| chr5:10639102 | C | G | 6 | a0001c0001t0042g0198 a0001c0004t0002g0139 a0001c0004t0002g0141 others(3): Show |
6 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+934C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639102 | |||||||
| chr5:10639102 | CGGTGACG others(24): Show |
C | 1 | a0002c0010t0018g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637+976_637+1006de others(32): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639102 | ||||||
| chr5:10639102 | CGGTGACG others(179): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.637+973_637+1158de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639102 | ||||||
| chr5:10639110 | C | T | 5 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0234 others(2): Show |
5 | HG00642.hp1 HG01109.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+942C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639110 | |||||||
| chr5:10639113 | A | G | 2 | a0001c0001t0001g0130 a0001c0004t0014g0111 |
2 | HG00642.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.637+945A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639113 | |||||||
| chr5:10639113 | AGTTGCGC others(303): Show |
A | 2 | a0001c0001t0033g0103 a0005c0027t0021g0004 |
2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.637+964_637+1273de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639113 | ||||||
| chr5:10639132 | C | G | 2 | a0001c0004t0014g0111 a0001c0007t0001g0192 |
2 | HG00642.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.637+964C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639132 | |||||||
| chr5:10639133 | G | C | 2 | a0001c0004t0014g0111 a0001c0007t0001g0192 |
2 | HG00642.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.637+965G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639133 | |||||||
| chr5:10639133 | G | GGGTGACG others(24): Show |
1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+972_637+973ins others(31): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639133 | ||||||
| chr5:10639133 | GGGTGACG others(55): Show |
G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0234 |
2 | HG01109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.637+973_637+1034de others(63): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639133 | ||||||
| chr5:10639133 | GGGTGACG others(210): Show |
G | 1 | a0001c0004t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.637+1007_637+1223d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639133 | ||||||
| chr5:10639141 | C | T | 2 | a0001c0001t0009g0260 a0001c0034t0001g0022 |
2 | HG03209.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.637+973C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639141 | |||||||
| chr5:10639141 | CGGAGTTG others(117): Show |
C | 2 | a0001c0001t0005g0165 a0001c0001t0005g0169 |
2 | HG00609.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.637+1007_637+1130d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639141 | ||||||
| chr5:10639144 | A | C | 2 | a0001c0001t0004g0090 a0001c0001t0048g0117 |
2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.637+976A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639144 | |||||||
| chr5:10639144 | A | G | 1 | a0001c0001t0009g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.637+976A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639144 | |||||||
| chr5:10639162 | GCGGGTGA others(116): Show |
G | 1 | a0001c0001t0048g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.637+995_637+1117de others(1): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639162 | |||||||
| chr5:10639163 | C | G | 5 | a0001c0001t0004g0090 a0001c0001t0009g0260 a0001c0001t0042g0198 others(2): Show |
5 | HG01070.hp1 HG01167.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+995C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639163 | |||||||
| chr5:10639164 | G | C | 5 | a0001c0001t0004g0090 a0001c0001t0009g0260 a0001c0001t0042g0198 others(2): Show |
5 | HG01070.hp1 HG01167.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+996G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639164 | |||||||
| chr5:10639172 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637+1004C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639172 | |||||||
| chr5:10639172 | CGGCGTTG others(24): Show |
C | 16 | a0001c0001t0001g0062 a0001c0001t0001g0244 a0001c0001t0001g0258 others(13): Show |
16 | HG00639.hp2 HG02015.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+1007_637+1037d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639172 | ||||||
| chr5:10639172 | CGGCGTTG others(86): Show |
C | 1 | a0001c0004t0014g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+1007_637+1099d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639172 | ||||||
| chr5:10639172 | CGGCGTTG others(148): Show |
C | 1 | a0001c0007t0001g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.637+1007_637+1161d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639172 | ||||||
| chr5:10639172 | CGGCGTTG others(365): Show |
C | 1 | a0001c0001t0001g0187 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.637+1007_637+1378d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639172 | ||||||
| chr5:10639172 | CGGCGTTG others(582): Show |
C | 1 | a0001c0004t0002g0293 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.637+1007_637+1595d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639172 | ||||||
| chr5:10639175 | C | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0130 a0001c0001t0001g0131 others(15): Show |
18 | HG01069.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.637+1007C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639175 | |||||||
| chr5:10639175 | C | G | 1 | a0001c0001t0004g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637+1007C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639175 | |||||||
| chr5:10639185 | C | T | 3 | a0003c0016t0001g0006 a0003c0016t0001g0010 a0003c0035t0001g0122 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.637+1017C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639185 | |||||||
| chr5:10639194 | G | C | 6 | a0001c0001t0001g0130 a0001c0001t0009g0260 a0001c0001t0042g0198 others(3): Show |
6 | HG01070.hp1 HG01167.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+1026G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639194 | |||||||
| chr5:10639195 | C | G | 6 | a0001c0001t0001g0130 a0001c0001t0009g0260 a0001c0001t0042g0198 others(3): Show |
6 | HG01070.hp1 HG01167.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+1027C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639195 | |||||||
| chr5:10639195 | CGGTGACG others(24): Show |
C | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637+1038_637+1068d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639195 | ||||||
| chr5:10639195 | CGGTGACG others(179): Show |
C | 1 | a0001c0001t0006g0286 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.637+1035_637+1220d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639195 | ||||||
| chr5:10639195 | CGGTGACG others(272): Show |
C | 7 | a0001c0001t0001g0131 a0001c0001t0032g0084 a0001c0001t0051g0315 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+1035_637+1313d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639195 | ||||||
| chr5:10639195 | CGGTGACG others(303): Show |
C | 1 | a0001c0001t0005g0185 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.637+1035_637+1344d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639195 | ||||||
| chr5:10639195 | CGGTGACG others(613): Show |
C | 1 | a0002c0010t0015g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.637+1035_637+1654d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639195 | ||||||
| chr5:10639196 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.637+1028G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639196 | |||||||
| chr5:10639202 | G | A | 7 | a0001c0006t0007g0191 a0001c0006t0007g0269 a0001c0014t0008g0018 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.637+1034G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639202 | |||||||
| chr5:10639203 | T | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0130 a0001c0001t0004g0090 others(17): Show |
20 | HG01070.hp1 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+1035T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639203 | |||||||
| chr5:10639203 | TGGAGTTG others(210): Show |
T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.637+1038_637+1254d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639203 | ||||||
| chr5:10639206 | A | G | 12 | a0001c0001t0001g0138 a0001c0001t0001g0166 a0001c0001t0001g0168 others(9): Show |
12 | HG00673.hp1 HG01109.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.637+1038A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639206 | |||||||
| chr5:10639206 | AGTTGCGC others(303): Show |
A | 1 | a0001c0033t0038g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.637+1057_637+1366d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639206 | ||||||
| chr5:10639224 | GCGGGTGA others(85): Show |
G | 1 | a0001c0001t0001g0209 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.637+1057_637+1148d others(94): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639224 | |||||||
| chr5:10639225 | C | G | 10 | a0001c0001t0001g0138 a0001c0001t0001g0171 a0001c0001t0001g0218 others(7): Show |
10 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+1057C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639225 | |||||||
| chr5:10639226 | G | C | 10 | a0001c0001t0001g0138 a0001c0001t0001g0171 a0001c0001t0001g0218 others(7): Show |
10 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+1058G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639226 | |||||||
| chr5:10639226 | GGGTGACG others(24): Show |
G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0250 a0001c0006t0003g0267 |
3 | HG00408.hp2 HG02155.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.637+1069_637+1099d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639226 | ||||||
| chr5:10639226 | GGGTGACG others(210): Show |
G | 1 | a0001c0001t0006g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.637+1066_637+1282d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639226 | ||||||
| chr5:10639234 | T | C | 19 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0168 others(16): Show |
19 | HG00099.hp1 HG01255.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+1066T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639234 | |||||||
| chr5:10639234 | TGGGGTTG others(179): Show |
T | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.637+1097_637+1282d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639234 | ||||||
| chr5:10639237 | G | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0138 a0001c0001t0001g0168 others(15): Show |
18 | HG00099.hp1 HG01109.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+1069G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639237 | |||||||
| chr5:10639237 | G | C | 2 | a0001c0001t0042g0198 a0001c0007t0001g0192 |
2 | HG02155.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.637+1069G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639237 | |||||||
| chr5:10639237 | GGTTGCGC others(148): Show |
G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637+1088_637+1242d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639237 | ||||||
| chr5:10639237 | GGTTGCGC others(303): Show |
G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0302 a0001c0001t0006g0012 others(14): Show |
17 | HG00558.hp1 HG01106.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.637+1159_637+1468d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639237 | ||||||
| chr5:10639242 | C | T | 1 | a0001c0001t0004g0092 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.637+1074C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639242 | |||||||
| chr5:10639244 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.637+1076C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639244 | |||||||
| chr5:10639256 | G | C | 16 | a0001c0001t0001g0043 a0001c0001t0001g0138 a0001c0001t0001g0168 others(13): Show |
16 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+1088G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639256 | |||||||
| chr5:10639257 | C | CGGTGACG others(24): Show |
3 | a0001c0001t0001g0237 a0001c0001t0009g0316 a0001c0001t0052g0025 |
3 | HG01261.hp1 HG02293.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.637+1096_637+1097i others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639257 | ||||||
| chr5:10639257 | C | G | 16 | a0001c0001t0001g0043 a0001c0001t0001g0138 a0001c0001t0001g0168 others(13): Show |
16 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+1089C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639257 | |||||||
| chr5:10639257 | CGGTGACG others(210): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.637+1097_637+1313d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639257 | ||||||
| chr5:10639265 | T | C | 80 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0060 others(77): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.637+1097T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639265 | |||||||
| chr5:10639265 | T | TGGAGTTG others(24): Show |
1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+1128_637+1158d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639265 | ||||||
| chr5:10639265 | T | TGTTGCGC others(52): Show |
1 | a0002c0010t0018g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637+1098_637+1099i others(61): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639265 | ||||||
| chr5:10639265 | TGGAGTTG others(334): Show |
T | 1 | a0001c0001t0042g0198 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637+1252_637+1592d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639265 | ||||||
| chr5:10639268 | A | C | 5 | a0001c0001t0001g0043 a0001c0001t0024g0206 a0001c0001t0031g0082 others(2): Show |
5 | HG02056.hp1 NA18964.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1100A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639268 | |||||||
| chr5:10639268 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637+1100A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639268 | |||||||
| chr5:10639287 | C | G | 5 | a0001c0001t0001g0043 a0001c0001t0024g0206 a0001c0001t0031g0082 others(2): Show |
5 | HG02056.hp1 NA18964.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1119C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639287 | |||||||
| chr5:10639287 | CG | C | 41 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0126 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.637+1122delG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639287 | ||||||
| chr5:10639288 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.637+1120G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639288 | |||||||
| chr5:10639288 | G | C | 5 | a0001c0001t0001g0043 a0001c0001t0024g0206 a0001c0001t0031g0082 others(2): Show |
5 | HG02056.hp1 NA18964.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1120G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639288 | |||||||
| chr5:10639288 | GGGTGACG others(55): Show |
G | 19 | a0001c0001t0001g0060 a0001c0001t0001g0142 a0001c0001t0001g0163 others(16): Show |
19 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+1159_637+1220d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639288 | ||||||
| chr5:10639288 | GGGTGACG others(148): Show |
G | 1 | a0001c0004t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.637+1159_637+1313d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639288 | ||||||
| chr5:10639295 | G | A | 40 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0126 others(37): Show |
40 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.637+1127G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639295 | |||||||
| chr5:10639296 | C | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0261 a0001c0001t0024g0206 others(5): Show |
8 | HG00597.hp1 HG01952.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+1128C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639296 | |||||||
| chr5:10639299 | A | G | 2 | a0001c0004t0002g0123 a0001c0007t0001g0192 |
2 | HG01952.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.637+1131A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639299 | |||||||
| chr5:10639299 | AGTTGCGC others(24): Show |
A | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.637+1150_637+1180d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639299 | ||||||
| chr5:10639310 | GATGTTAG others(768): Show |
G | 5 | a0001c0001t0001g0218 a0001c0001t0001g0274 a0001c0001t0001g0301 others(2): Show |
5 | HG00673.hp1 HG02027.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1162_637+1936d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639310 | ||||||
| chr5:10639318 | C | G | 2 | a0001c0004t0002g0123 a0001c0007t0001g0192 |
2 | HG01952.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.637+1150C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639318 | |||||||
| chr5:10639319 | G | C | 2 | a0001c0004t0002g0123 a0001c0007t0001g0192 |
2 | HG01952.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.637+1151G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639319 | |||||||
| chr5:10639319 | GGGTGACG others(24): Show |
G | 3 | a0001c0001t0001g0027 a0001c0004t0014g0108 a0001c0004t0039g0217 |
3 | HG01255.hp2 HG01258.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.637+1159_637+1189d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639319 | ||||||
| chr5:10639319 | GGGTGACG others(117): Show |
G | 1 | a0001c0001t0068g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.637+1159_637+1282d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639319 | ||||||
| chr5:10639319 | GGGTGACG others(210): Show |
G | 1 | a0002c0010t0018g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637+1162_637+1378d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639319 | ||||||
| chr5:10639327 | T | C | 62 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0126 others(59): Show |
62 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.637+1159T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639327 | |||||||
| chr5:10639327 | TGGGGTTG others(86): Show |
T | 12 | a0001c0001t0001g0244 a0001c0001t0001g0258 a0001c0001t0005g0050 others(9): Show |
12 | HG02015.hp1 HG02071.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+1255_637+1347d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639327 | ||||||
| chr5:10639330 | G | A | 59 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0126 others(56): Show |
59 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.637+1162G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639330 | |||||||
| chr5:10639330 | G | C | 3 | a0001c0001t0001g0237 a0001c0001t0004g0090 a0001c0001t0009g0260 |
3 | HG01261.hp1 HG02080.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.637+1162G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639330 | |||||||
| chr5:10639330 | GGTTGCGC others(24): Show |
G | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.637+1181_637+1211d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639330 | ||||||
| chr5:10639348 | G | GCGGGTGA others(85): Show |
1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1180_637+1181i others(94): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639348 | |||||||
| chr5:10639349 | G | C | 13 | a0001c0001t0001g0209 a0001c0001t0001g0222 a0001c0001t0001g0281 others(10): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.637+1181G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639349 | |||||||
| chr5:10639350 | C | G | 13 | a0001c0001t0001g0209 a0001c0001t0001g0222 a0001c0001t0001g0281 others(10): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.637+1182C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639350 | |||||||
| chr5:10639350 | CGGTGACG others(24): Show |
C | 1 | a0001c0004t0014g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+1224_637+1254d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639350 | ||||||
| chr5:10639350 | CGGTGACG others(241): Show |
C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0171 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.637+1252_637+1499d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639350 | ||||||
| chr5:10639358 | C | T | 9 | a0001c0001t0001g0222 a0001c0001t0001g0281 a0001c0001t0001g0310 others(6): Show |
9 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1190C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639358 | |||||||
| chr5:10639358 | CGGAGTTG others(210): Show |
C | 2 | a0001c0001t0001g0162 a0001c0001t0054g0033 |
2 | HG01109.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.637+1255_637+1471d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639358 | ||||||
| chr5:10639361 | A | G | 9 | a0001c0001t0001g0222 a0001c0001t0001g0281 a0001c0001t0001g0310 others(6): Show |
9 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1193A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639361 | |||||||
| chr5:10639361 | AGTTGCGC others(55): Show |
A | 1 | a0001c0001t0009g0202 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.637+1212_637+1273d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639361 | ||||||
| chr5:10639380 | C | G | 8 | a0001c0001t0001g0222 a0001c0001t0001g0281 a0001c0001t0001g0310 others(5): Show |
8 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+1212C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639380 | |||||||
| chr5:10639381 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0190 others(2): Show |
5 | HG00099.hp2 HG01981.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1213G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639381 | |||||||
| chr5:10639381 | G | C | 8 | a0001c0001t0001g0222 a0001c0001t0001g0281 a0001c0001t0001g0310 others(5): Show |
8 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+1213G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639381 | |||||||
| chr5:10639381 | G | GGGTGACG others(86): Show |
1 | a0001c0004t0040g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.637+1223_637+1224i others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639381 | ||||||
| chr5:10639389 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0009g0260 a0001c0004t0014g0108 others(1): Show |
4 | HG01255.hp2 HG01258.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1221C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639389 | |||||||
| chr5:10639392 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0009g0260 a0001c0004t0014g0108 others(1): Show |
4 | HG01255.hp2 HG01258.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1224A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639392 | |||||||
| chr5:10639397 | CGCGGCGA others(489): Show |
C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0250 a0001c0001t0031g0082 |
3 | HG00408.hp2 HG02056.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.637+1252_637+1747d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639397 | ||||||
| chr5:10639411 | C | G | 5 | a0001c0001t0001g0027 a0001c0001t0009g0260 a0001c0001t0065g0102 others(2): Show |
5 | HG01255.hp2 HG01258.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1243C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639411 | |||||||
| chr5:10639412 | G | C | 5 | a0001c0001t0001g0027 a0001c0001t0009g0260 a0001c0001t0065g0102 others(2): Show |
5 | HG01255.hp2 HG01258.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1244G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639412 | |||||||
| chr5:10639412 | GGGTGACG others(117): Show |
G | 1 | a0001c0006t0003g0267 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.637+1252_637+1375d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639412 | ||||||
| chr5:10639420 | C | T | 34 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0138 others(31): Show |
34 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.637+1252C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639420 | |||||||
| chr5:10639420 | CGGGGTTG others(117): Show |
C | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.637+1255_637+1378d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639420 | ||||||
| chr5:10639423 | G | A | 67 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0115 others(64): Show |
67 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.637+1255G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639423 | |||||||
| chr5:10639423 | G | C | 11 | a0001c0001t0001g0062 a0001c0001t0005g0118 a0001c0001t0065g0102 others(8): Show |
11 | HG00639.hp2 HG02647.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.637+1255G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639423 | |||||||
| chr5:10639428 | CGCGGCGA others(458): Show |
C | 2 | a0001c0001t0024g0206 a0001c0007t0024g0155 |
2 | NA18975.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.637+1274_637+1738d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639428 | ||||||
| chr5:10639442 | G | C | 16 | a0001c0001t0001g0222 a0001c0001t0001g0245 a0001c0001t0001g0246 others(13): Show |
16 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+1274G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639442 | |||||||
| chr5:10639443 | C | G | 16 | a0001c0001t0001g0222 a0001c0001t0001g0245 a0001c0001t0001g0246 others(13): Show |
16 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+1275C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639443 | |||||||
| chr5:10639443 | CGGTGACG others(24): Show |
C | 1 | a0001c0014t0008g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.637+1317_637+1347d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639443 | ||||||
| chr5:10639451 | C | T | 18 | a0001c0001t0001g0062 a0001c0001t0001g0219 a0001c0001t0001g0222 others(15): Show |
18 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.637+1283C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639451 | |||||||
| chr5:10639454 | A | C | 2 | a0001c0001t0001g0264 a0001c0001t0009g0134 |
2 | HG01123.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.637+1286A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639454 | |||||||
| chr5:10639454 | A | G | 8 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0281 others(5): Show |
8 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+1286A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639454 | |||||||
| chr5:10639473 | C | G | 11 | a0001c0001t0001g0062 a0001c0001t0001g0222 a0001c0001t0001g0281 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+1305C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639473 | |||||||
| chr5:10639474 | G | C | 11 | a0001c0001t0001g0062 a0001c0001t0001g0222 a0001c0001t0001g0281 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+1306G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639474 | |||||||
| chr5:10639474 | G | GGGTGACG others(24): Show |
1 | a0001c0001t0006g0283 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637+1313_637+1314i others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639474 | ||||||
| chr5:10639474 | GGGTGACG others(55): Show |
G | 4 | a0001c0006t0007g0191 a0001c0006t0007g0269 a0001c0007t0001g0154 others(1): Show |
4 | HG03486.hp1 NA18966.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1314_637+1375d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639474 | ||||||
| chr5:10639474 | GGGTGACG others(303): Show |
G | 1 | a0001c0001t0065g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.637+1348_637+1657d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639474 | ||||||
| chr5:10639482 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0005g0118 a0001c0001t0009g0134 others(2): Show |
5 | HG00639.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1314C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639482 | |||||||
| chr5:10639482 | CGGAGTTG others(86): Show |
C | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.637+1348_637+1440d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639482 | ||||||
| chr5:10639485 | A | C | 4 | a0001c0001t0006g0284 a0001c0001t0033g0103 a0001c0001t0068g0204 others(1): Show |
4 | HG02486.hp2 HG02976.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1317A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639485 | |||||||
| chr5:10639485 | A | G | 3 | a0001c0004t0039g0217 a0001c0004t0040g0266 a0001c0007t0005g0179 |
3 | HG01255.hp2 HG03688.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.637+1317A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639485 | |||||||
| chr5:10639504 | C | G | 4 | a0001c0001t0006g0284 a0001c0001t0009g0134 a0001c0001t0068g0204 others(1): Show |
4 | HG01123.hp1 HG02486.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1336C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639504 | |||||||
| chr5:10639505 | G | C | 4 | a0001c0001t0006g0284 a0001c0001t0009g0134 a0001c0001t0068g0204 others(1): Show |
4 | HG01123.hp1 HG02486.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1337G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639505 | |||||||
| chr5:10639505 | GGGTGACG others(24): Show |
G | 2 | a0001c0001t0004g0081 a0001c0007t0001g0192 |
2 | HG02155.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.637+1345_637+1375d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639505 | ||||||
| chr5:10639505 | GGGTGACG others(179): Show |
G | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.637+1348_637+1533d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639505 | ||||||
| chr5:10639513 | C | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0203 others(15): Show |
18 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+1345C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639513 | |||||||
| chr5:10639513 | CGGCGTTG others(55): Show |
C | 1 | a0001c0006t0058g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.637+1348_637+1409d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639513 | ||||||
| chr5:10639516 | C | A | 25 | a0001c0001t0001g0131 a0001c0001t0001g0219 a0001c0001t0001g0222 others(22): Show |
25 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.637+1348C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639516 | |||||||
| chr5:10639516 | C | G | 17 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0203 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.637+1348C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639516 | |||||||
| chr5:10639516 | CGTTGCGC others(24): Show |
C | 9 | a0001c0001t0001g0138 a0001c0001t0001g0190 a0001c0001t0001g0300 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+1398_637+1428d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639516 | ||||||
| chr5:10639516 | CGTTGCGC others(24): Show |
G | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637+1348_637+1379d others(38): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639516 | |||||||
| chr5:10639516 | CGTTGCGC others(148): Show |
C | 1 | a0001c0007t0001g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.637+1376_637+1530d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639516 | ||||||
| chr5:10639535 | G | C | 24 | a0001c0001t0001g0131 a0001c0001t0001g0219 a0001c0001t0001g0222 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+1367G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639535 | |||||||
| chr5:10639536 | C | G | 24 | a0001c0001t0001g0131 a0001c0001t0001g0219 a0001c0001t0001g0222 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+1368C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639536 | |||||||
| chr5:10639544 | T | C | 34 | a0001c0001t0001g0060 a0001c0001t0001g0131 a0001c0001t0001g0159 others(31): Show |
34 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.637+1376T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639544 | |||||||
| chr5:10639544 | TGGAGTTG others(55): Show |
T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0012g0019 |
3 | NA19084.hp1 NA19088.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.637+1398_637+1459d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639544 | ||||||
| chr5:10639544 | TGGAGTTG others(86): Show |
T | 1 | a0001c0001t0009g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.637+1398_637+1490d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639544 | ||||||
| chr5:10639544 | TGGAGTTG others(179): Show |
T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0240 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.637+1398_637+1583d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639544 | ||||||
| chr5:10639547 | A | AGTTGCGC others(24): Show |
1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+1397_637+1398i others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639547 | ||||||
| chr5:10639547 | A | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0281 others(11): Show |
14 | HG00280.hp1 HG01069.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.637+1379A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639547 | |||||||
| chr5:10639547 | A | G | 12 | a0001c0001t0001g0222 a0001c0001t0004g0081 a0001c0001t0005g0185 others(9): Show |
12 | HG02155.hp1 HG02155.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.637+1379A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639547 | |||||||
| chr5:10639552 | CGCGGCGA others(334): Show |
C | 3 | a0003c0016t0001g0006 a0003c0016t0001g0010 a0003c0035t0001g0122 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.637+1398_637+1738d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639552 | ||||||
| chr5:10639566 | G | C | 65 | a0001c0001t0001g0060 a0001c0001t0001g0115 a0001c0001t0001g0121 others(62): Show |
65 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.637+1398G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639566 | |||||||
| chr5:10639567 | C | G | 65 | a0001c0001t0001g0060 a0001c0001t0001g0115 a0001c0001t0001g0121 others(62): Show |
65 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.637+1399C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639567 | |||||||
| chr5:10639567 | CGGTGACG others(24): Show |
C | 1 | a0001c0007t0005g0179 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.637+1407_637+1437d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639567 | ||||||
| chr5:10639575 | T | C | 40 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0138 others(37): Show |
40 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.637+1407T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639575 | |||||||
| chr5:10639575 | TGGAGTTG others(24): Show |
T | 1 | a0001c0001t0006g0286 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.637+1469_637+1499d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639575 | ||||||
| chr5:10639578 | A | G | 50 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0126 others(47): Show |
50 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.637+1410A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639578 | |||||||
| chr5:10639588 | C | T | 1 | a0001c0013t0011g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.637+1420C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639588 | |||||||
| chr5:10639597 | C | G | 58 | a0001c0001t0001g0066 a0001c0001t0001g0115 a0001c0001t0001g0121 others(55): Show |
58 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.637+1429C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639597 | |||||||
| chr5:10639598 | G | C | 58 | a0001c0001t0001g0066 a0001c0001t0001g0115 a0001c0001t0001g0121 others(55): Show |
58 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.637+1430G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639598 | |||||||
| chr5:10639598 | GGGTGACG others(86): Show |
G | 5 | a0001c0001t0001g0131 a0001c0001t0051g0315 a0001c0015t0001g0243 others(2): Show |
5 | HG02055.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1593_637+1685d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639598 | ||||||
| chr5:10639606 | C | T | 48 | a0001c0001t0001g0066 a0001c0001t0001g0115 a0001c0001t0001g0121 others(45): Show |
48 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.637+1438C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639606 | |||||||
| chr5:10639609 | A | C | 8 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0203 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+1441A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639609 | |||||||
| chr5:10639609 | A | G | 10 | a0001c0001t0001g0211 a0001c0001t0006g0296 a0001c0001t0006g0297 others(7): Show |
10 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+1441A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639609 | |||||||
| chr5:10639619 | C | T | 1 | a0001c0001t0005g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.637+1451C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639619 | |||||||
| chr5:10639628 | C | G | 15 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0203 others(12): Show |
15 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+1460C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639628 | |||||||
| chr5:10639629 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.637+1461G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639629 | |||||||
| chr5:10639629 | G | C | 15 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0203 others(12): Show |
15 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+1461G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639629 | |||||||
| chr5:10639629 | GGGTGACG others(55): Show |
G | 39 | a0001c0001t0001g0066 a0001c0001t0001g0115 a0001c0001t0001g0121 others(36): Show |
39 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.637+1500_637+1561d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639629 | ||||||
| chr5:10639637 | C | T | 15 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0203 others(12): Show |
15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+1469C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639637 | |||||||
| chr5:10639637 | CGGAGTTG others(272): Show |
C | 1 | a0001c0001t0001g0209 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.637+1472_637+1750d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639637 | ||||||
| chr5:10639640 | A | C | 5 | a0001c0001t0001g0187 a0001c0001t0054g0033 a0001c0004t0002g0298 others(2): Show |
5 | HG01109.hp2 HG01515.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1472A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639640 | |||||||
| chr5:10639640 | A | G | 5 | a0001c0001t0009g0134 a0001c0001t0012g0019 a0001c0001t0042g0198 others(2): Show |
5 | HG01123.hp1 HG02602.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1472A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639640 | |||||||
| chr5:10639659 | C | G | 15 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0187 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+1491C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639659 | |||||||
| chr5:10639660 | G | C | 15 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0187 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+1492G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639660 | |||||||
| chr5:10639660 | GGGTGACG others(24): Show |
G | 4 | a0001c0001t0032g0084 a0001c0004t0002g0139 a0001c0004t0002g0141 others(1): Show |
4 | HG01069.hp1 HG01070.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1500_637+1530d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639660 | ||||||
| chr5:10639668 | T | C | 22 | a0001c0001t0001g0130 a0001c0001t0001g0156 a0001c0001t0001g0166 others(19): Show |
22 | HG00642.hp2 HG01123.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.637+1500T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639668 | |||||||
| chr5:10639671 | G | A | 20 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0187 others(17): Show |
20 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.637+1503G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639671 | |||||||
| chr5:10639671 | G | C | 2 | a0001c0001t0009g0260 a0002c0010t0018g0307 |
2 | HG03540.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.637+1503G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639671 | |||||||
| chr5:10639671 | GGTTGCGC others(24): Show |
G | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+1522_637+1552d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639671 | ||||||
| chr5:10639671 | GGTTGCGC others(148): Show |
G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637+1522_637+1676d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639671 | ||||||
| chr5:10639690 | G | C | 19 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0187 others(16): Show |
19 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+1522G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639690 | |||||||
| chr5:10639691 | C | CGGTGACG others(55): Show |
1 | a0002c0010t0018g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637+1530_637+1531i others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639691 | ||||||
| chr5:10639691 | C | G | 19 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0001g0187 others(16): Show |
19 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+1523C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639691 | |||||||
| chr5:10639691 | CGGTGACG others(272): Show |
C | 1 | a0001c0007t0001g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.637+1562_637+1840d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639691 | ||||||
| chr5:10639699 | C | T | 3 | a0001c0001t0009g0034 a0001c0001t0009g0260 a0001c0004t0002g0298 |
3 | HG02735.hp1 HG03834.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.637+1531C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639699 | |||||||
| chr5:10639702 | A | C | 3 | a0001c0004t0002g0143 a0001c0004t0014g0108 a0001c0004t0039g0217 |
3 | HG00642.hp2 HG01255.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.637+1534A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639702 | |||||||
| chr5:10639702 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.637+1534A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639702 | |||||||
| chr5:10639702 | AGTTGCGC others(55): Show |
A | 2 | a0001c0006t0007g0191 a0001c0006t0007g0269 |
2 | NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.637+1553_637+1614d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639702 | ||||||
| chr5:10639707 | CGCGGCGA others(179): Show |
C | 2 | a0001c0001t0001g0305 a0001c0011t0001g0001 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.637+1562_637+1747d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639707 | ||||||
| chr5:10639712 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.637+1544C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639712 | |||||||
| chr5:10639720 | GCGGGTGA others(240): Show |
G | 1 | a0001c0033t0038g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.637+1553_637+1799d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639720 | |||||||
| chr5:10639721 | C | G | 7 | a0001c0001t0001g0187 a0001c0001t0001g0237 a0001c0001t0009g0260 others(4): Show |
7 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+1553C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639721 | |||||||
| chr5:10639722 | G | A | 2 | a0001c0001t0026g0167 a0001c0001t0026g0210 |
2 | NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.637+1554G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639722 | |||||||
| chr5:10639722 | G | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0237 a0001c0001t0009g0260 others(4): Show |
7 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+1554G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639722 | |||||||
| chr5:10639722 | GGGTGACG others(55): Show |
G | 1 | a0001c0004t0002g0298 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.637+1593_637+1654d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639722 | ||||||
| chr5:10639730 | C | CGGCGTTG others(24): Show |
1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+1564_637+1565i others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639730 | ||||||
| chr5:10639730 | C | T | 7 | a0001c0001t0001g0187 a0001c0001t0009g0260 a0001c0004t0002g0143 others(4): Show |
7 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+1562C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639730 | |||||||
| chr5:10639730 | CGGAGTTG others(272): Show |
C | 9 | a0001c0001t0001g0244 a0001c0001t0005g0050 a0001c0001t0005g0052 others(6): Show |
9 | HG00609.hp2 HG02015.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+1596_637+1874d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639730 | ||||||
| chr5:10639733 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.637+1565A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639733 | |||||||
| chr5:10639733 | A | G | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+1565A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639733 | |||||||
| chr5:10639740 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.637+1572C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639740 | |||||||
| chr5:10639752 | C | G | 5 | a0001c0004t0002g0143 a0001c0004t0014g0108 a0001c0004t0039g0217 others(2): Show |
5 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1584C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639752 | |||||||
| chr5:10639753 | G | C | 5 | a0001c0004t0002g0143 a0001c0004t0014g0108 a0001c0004t0039g0217 others(2): Show |
5 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1585G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639753 | |||||||
| chr5:10639753 | GGGTGACG others(24): Show |
G | 1 | a0001c0001t0009g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.637+1593_637+1623d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639753 | ||||||
| chr5:10639753 | GGGTGACG others(117): Show |
G | 2 | a0001c0001t0004g0081 a0001c0004t0002g0256 |
2 | HG01192.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.637+1596_637+1719d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639753 | ||||||
| chr5:10639761 | T | C | 14 | a0001c0001t0001g0076 a0001c0001t0001g0219 a0001c0001t0001g0222 others(11): Show |
14 | HG00140.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+1593T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639761 | |||||||
| chr5:10639764 | G | A | 14 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0001t0009g0034 others(11): Show |
14 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.637+1596G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639764 | |||||||
| chr5:10639764 | G | C | 5 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0005g0118 others(2): Show |
5 | HG00140.hp2 HG03453.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1596G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639764 | |||||||
| chr5:10639774 | C | T | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+1606C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639774 | |||||||
| chr5:10639783 | G | C | 6 | a0001c0001t0009g0034 a0001c0004t0002g0143 a0001c0004t0014g0108 others(3): Show |
6 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+1615G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639783 | |||||||
| chr5:10639784 | C | G | 6 | a0001c0001t0009g0034 a0001c0004t0002g0143 a0001c0004t0014g0108 others(3): Show |
6 | HG00642.hp2 HG01255.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+1616C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639784 | |||||||
| chr5:10639784 | CGGTGACG others(24): Show |
C | 1 | a0001c0001t0006g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637+1658_637+1688d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639784 | ||||||
| chr5:10639792 | C | T | 6 | a0001c0001t0001g0222 a0001c0001t0005g0118 a0001c0001t0009g0034 others(3): Show |
6 | HG00140.hp2 HG02615.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+1624C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639792 | |||||||
| chr5:10639795 | A | G | 1 | a0001c0001t0009g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.637+1627A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639795 | |||||||
| chr5:10639805 | C | T | 1 | a0001c0026t0008g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+1637C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639805 | |||||||
| chr5:10639805 | CGATGTTA others(148): Show |
C | 1 | a0001c0001t0004g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637+1686_637+1840d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639805 | ||||||
| chr5:10639808 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0300 a0001c0004t0002g0144 |
3 | HG01106.hp1 HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.637+1640T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639808 | |||||||
| chr5:10639814 | C | G | 5 | a0001c0001t0001g0222 a0001c0001t0005g0118 a0001c0001t0009g0034 others(2): Show |
5 | HG00140.hp2 HG02735.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1646C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639814 | |||||||
| chr5:10639815 | G | C | 5 | a0001c0001t0001g0222 a0001c0001t0005g0118 a0001c0001t0009g0034 others(2): Show |
5 | HG00140.hp2 HG02735.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1647G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639815 | |||||||
| chr5:10639823 | C | T | 5 | a0001c0001t0001g0222 a0001c0001t0005g0118 a0001c0001t0052g0025 others(2): Show |
5 | HG00140.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1655C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639823 | |||||||
| chr5:10639823 | CGGAGTTG others(179): Show |
C | 32 | a0001c0001t0001g0027 a0001c0001t0001g0156 a0001c0001t0001g0159 others(29): Show |
32 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.637+1686_637+1871d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639823 | ||||||
| chr5:10639826 | A | G | 1 | a0001c0004t0002g0298 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.637+1658A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639826 | |||||||
| chr5:10639831 | CGCGGCGA others(55): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.637+1686_637+1747d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639831 | ||||||
| chr5:10639836 | C | CGATGTTA others(86): Show |
1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+1685_637+1686i others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639836 | ||||||
| chr5:10639854 | C | T | 25 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0066 others(22): Show |
25 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.637+1686C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639854 | |||||||
| chr5:10639854 | CGGCGTTG others(210): Show |
C | 1 | a0001c0001t0009g0316 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.637+1689_637+1905d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639854 | ||||||
| chr5:10639857 | C | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0222 a0001c0001t0052g0025 others(2): Show |
5 | HG00099.hp1 HG00140.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1689C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639857 | |||||||
| chr5:10639857 | C | G | 25 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0066 others(22): Show |
25 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.637+1689C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639857 | |||||||
| chr5:10639857 | CGTTGCGC others(55): Show |
C | 1 | a0001c0006t0007g0191 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.637+1725_637+1786d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639857 | ||||||
| chr5:10639863 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1695G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639863 | |||||||
| chr5:10639867 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1699C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639867 | |||||||
| chr5:10639876 | G | C | 4 | a0001c0001t0001g0222 a0001c0001t0052g0025 a0001c0001t0066g0110 others(1): Show |
4 | HG00140.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1708G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639876 | |||||||
| chr5:10639877 | C | CGGTGACG others(24): Show |
1 | a0002c0010t0018g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637+1716_637+1717i others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639877 | ||||||
| chr5:10639877 | C | G | 4 | a0001c0001t0001g0222 a0001c0001t0052g0025 a0001c0001t0066g0110 others(1): Show |
4 | HG00140.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1709C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639877 | |||||||
| chr5:10639877 | CGGTGACG others(86): Show |
C | 13 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0066 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+1717_637+1809d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639877 | ||||||
| chr5:10639877 | CGGTGACG others(117): Show |
C | 1 | a0001c0001t0057g0038 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637+1725_637+1848d others(2): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639877 | ||||||
| chr5:10639885 | T | C | 15 | a0001c0001t0001g0222 a0001c0001t0004g0081 a0001c0001t0005g0118 others(12): Show |
15 | HG00140.hp2 HG00642.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+1717T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639885 | |||||||
| chr5:10639885 | TGGAGTTG others(86): Show |
T | 1 | a0001c0001t0054g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.637+1725_637+1817d others(95): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639885 | ||||||
| chr5:10639886 | G | A | 6 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0113 others(3): Show |
6 | HG01106.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+1718G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639886 | |||||||
| chr5:10639893 | T | C | 124 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0065 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.637+1725T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639893 | |||||||
| chr5:10639894 | G | A | 1 | a0001c0034t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+1726G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639894 | |||||||
| chr5:10639895 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1727C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639895 | |||||||
| chr5:10639898 | C | T | 2 | a0001c0001t0001g0171 a0001c0034t0001g0022 |
2 | HG00099.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.637+1730C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639898 | |||||||
| chr5:10639899 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1731G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639899 | |||||||
| chr5:10639906 | GCGGGTGA others(54): Show |
G | 1 | a0001c0001t0056g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.637+1739_637+1799d others(63): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639906 | |||||||
| chr5:10639907 | C | G | 2 | a0001c0001t0001g0237 a0001c0034t0001g0022 |
2 | HG01261.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.637+1739C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639907 | |||||||
| chr5:10639908 | G | C | 2 | a0001c0001t0001g0237 a0001c0034t0001g0022 |
2 | HG01261.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.637+1740G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639908 | |||||||
| chr5:10639908 | G | GGGTGACG others(55): Show |
1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1747_637+1748i others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639908 | ||||||
| chr5:10639908 | GGGTGACG others(24): Show |
G | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1751_637+1781d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639908 | ||||||
| chr5:10639916 | T | C | 16 | a0001c0001t0001g0076 a0001c0001t0005g0118 a0001c0001t0006g0024 others(13): Show |
16 | HG00140.hp2 HG00642.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+1748T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639916 | |||||||
| chr5:10639919 | G | A | 22 | a0001c0001t0001g0076 a0001c0001t0001g0237 a0001c0001t0001g0250 others(19): Show |
22 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.637+1751G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639919 | |||||||
| chr5:10639925 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.637+1757G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639925 | |||||||
| chr5:10639929 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.637+1761C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639929 | |||||||
| chr5:10639937 | G | GCGGGTGA others(54): Show |
1 | a0001c0001t0006g0283 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637+1769_637+1770i others(63): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639937 | |||||||
| chr5:10639938 | G | C | 10 | a0001c0001t0001g0237 a0001c0001t0005g0118 a0001c0001t0009g0260 others(7): Show |
10 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.637+1770G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639938 | |||||||
| chr5:10639939 | C | G | 10 | a0001c0001t0001g0237 a0001c0001t0005g0118 a0001c0001t0009g0260 others(7): Show |
10 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.637+1771C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639939 | |||||||
| chr5:10639939 | CGGTGACG others(24): Show |
C | 10 | a0001c0001t0001g0076 a0001c0001t0004g0081 a0001c0001t0006g0024 others(7): Show |
10 | HG01192.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+1779_637+1809d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639939 | ||||||
| chr5:10639939 | CGGTGACG others(55): Show |
C | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.637+1792_637+1853d others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639939 | ||||||
| chr5:10639947 | T | C | 4 | a0001c0001t0001g0163 a0001c0001t0001g0237 a0001c0001t0009g0134 others(1): Show |
4 | HG01123.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1779T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639947 | |||||||
| chr5:10639950 | A | G | 9 | a0001c0001t0005g0118 a0001c0001t0009g0260 a0001c0001t0012g0288 others(6): Show |
9 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1782A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639950 | |||||||
| chr5:10639957 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.637+1789C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639957 | |||||||
| chr5:10639960 | T | C | 19 | a0001c0001t0001g0163 a0001c0001t0001g0209 a0001c0001t0001g0237 others(16): Show |
19 | HG00140.hp2 HG00642.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+1792T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639960 | |||||||
| chr5:10639961 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.637+1793G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639961 | |||||||
| chr5:10639969 | C | G | 9 | a0001c0001t0005g0118 a0001c0001t0009g0260 a0001c0001t0012g0288 others(6): Show |
9 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1801C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639969 | |||||||
| chr5:10639970 | G | C | 9 | a0001c0001t0005g0118 a0001c0001t0009g0260 a0001c0001t0012g0288 others(6): Show |
9 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1802G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639970 | |||||||
| chr5:10639970 | G | GGGTGACG others(55): Show |
1 | a0001c0001t0009g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.637+1840_637+1841i others(64): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10639970 | ||||||
| chr5:10639978 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0250 a0001c0001t0012g0288 |
3 | HG00099.hp1 HG00408.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.637+1810C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639978 | |||||||
| chr5:10639986 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1818C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639986 | |||||||
| chr5:10639988 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1820C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639988 | |||||||
| chr5:10639991 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0012g0288 |
2 | HG00099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.637+1823C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10639991 | |||||||
| chr5:10640007 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+1839C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640007 | |||||||
| chr5:10640009 | T | C | 43 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0066 others(40): Show |
43 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.637+1841T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640009 | |||||||
| chr5:10640009 | T | TGGGGTTG others(148): Show |
1 | a0001c0001t0001g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.637+1843_637+1844i others(157): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10640009 | ||||||
| chr5:10640049 | A | G | 5 | a0001c0001t0001g0237 a0001c0001t0006g0015 a0001c0001t0009g0134 others(2): Show |
5 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1881A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640049 | |||||||
| chr5:10640050 | C | T | 2 | a0001c0001t0009g0134 a0001c0001t0009g0202 |
2 | HG01123.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.637+1882C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640050 | |||||||
| chr5:10640053 | T | C | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1885T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640053 | |||||||
| chr5:10640054 | G | A | 3 | a0001c0001t0009g0134 a0001c0001t0009g0202 a0002c0010t0018g0307 |
3 | HG01123.hp1 HG02004.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637+1886G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640054 | |||||||
| chr5:10640062 | G | C | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1894G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640062 | |||||||
| chr5:10640063 | C | G | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1895C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640063 | |||||||
| chr5:10640071 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.637+1903T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640071 | |||||||
| chr5:10640080 | G | A | 11 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0001t0012g0288 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+1912G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640080 | |||||||
| chr5:10640081 | T | C | 13 | a0001c0001t0001g0076 a0001c0001t0001g0242 a0001c0001t0006g0024 others(10): Show |
13 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.637+1913T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640081 | |||||||
| chr5:10640085 | A | G | 12 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0001t0012g0019 others(9): Show |
12 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.637+1917A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640085 | |||||||
| chr5:10640085 | AATGTTAG others(24): Show |
A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0004g0090 |
3 | HG02080.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637+1942_637+1972d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10640085 | ||||||
| chr5:10640093 | C | G | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1925C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640093 | |||||||
| chr5:10640094 | G | C | 1 | a0001c0001t0012g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+1926G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640094 | |||||||
| chr5:10640102 | T | C | 113 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.637+1934T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640102 | |||||||
| chr5:10640110 | C | T | 1 | a0001c0001t0012g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637+1942C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640110 | |||||||
| chr5:10640112 | C | T | 1 | a0001c0001t0012g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637+1944C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640112 | |||||||
| chr5:10640112 | CGGTGATG others(24): Show |
C | 2 | a0001c0001t0001g0131 a0001c0001t0051g0315 |
2 | NA18974.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.637+1963_637+1993d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10640112 | ||||||
| chr5:10640115 | T | C | 113 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.637+1947T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640115 | |||||||
| chr5:10640131 | CGTGGAGT others(24): Show |
C | 1 | a0001c0001t0001g0281 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.637+1973_637+2003d others(33): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10640131 | ||||||
| chr5:10640133 | T | C | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+1965T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640133 | |||||||
| chr5:10640134 | G | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+1966G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640134 | |||||||
| chr5:10640156 | G | A | 3 | a0003c0016t0001g0006 a0003c0016t0001g0010 a0003c0035t0001g0122 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.637+1988G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640156 | |||||||
| chr5:10640191 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+2023A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640191 | |||||||
| chr5:10640357 | C | T | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.637+2189C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640357 | |||||||
| chr5:10640387 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+2219G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640387 | |||||||
| chr5:10640451 | C | G | 2 | a0003c0019t0028g0011 a0003c0019t0028g0232 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.637+2283C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640451 | |||||||
| chr5:10640542 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+2374A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640542 | |||||||
| chr5:10640699 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+2531G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640699 | |||||||
| chr5:10640753 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.637+2585A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640753 | |||||||
| chr5:10640769 | C | G | 3 | a0003c0016t0001g0006 a0003c0016t0001g0010 a0003c0035t0001g0122 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.637+2601C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640769 | |||||||
| chr5:10640781 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+2613G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640781 | |||||||
| chr5:10640804 | A | G | 2 | a0001c0004t0002g0139 a0001c0004t0002g0141 |
2 | HG01070.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.637+2636A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640804 | |||||||
| chr5:10640816 | G | A | 1 | a0001c0007t0001g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.637+2648G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640816 | |||||||
| chr5:10640900 | G | C | 1 | a0002c0010t0018g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637+2732G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10640900 | |||||||
| chr5:10641028 | C | T | 1 | a0007c0022t0020g0005 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.637+2860C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641028 | |||||||
| chr5:10641051 | C | T | 1 | a0010c0029t0041g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.637+2883C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641051 | |||||||
| chr5:10641068 | C | T | 16 | a0001c0002t0001g0137 a0001c0002t0001g0147 a0001c0002t0001g0148 others(13): Show |
16 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+2900C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641068 | |||||||
| chr5:10641208 | G | GTCTTCTT others(2): Show |
27 | a0001c0002t0001g0175 a0001c0002t0001g0230 a0001c0002t0001g0265 others(24): Show |
27 | HG00673.hp2 HG00741.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.637+3051_637+3059d others(11): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641208 | ||||||
| chr5:10641208 | GTCTTCT | G | 8 | a0001c0003t0007g0213 a0003c0019t0028g0011 a0003c0019t0028g0232 others(5): Show |
8 | HG02258.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+3054_637+3059d others(8): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641208 | ||||||
| chr5:10641225 | C | CT | 12 | a0001c0001t0001g0190 a0001c0001t0001g0228 a0001c0001t0001g0238 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.637+3080dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641225 | ||||||
| chr5:10641225 | C | CTTCTTCT others(3): Show |
61 | a0001c0002t0001g0040 a0001c0002t0001g0063 a0001c0002t0001g0064 others(58): Show |
61 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.637+3059_637+3060i others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641225 | ||||||
| chr5:10641225 | C | CTTCTTCT others(4): Show |
2 | a0001c0002t0001g0069 a0001c0002t0001g0224 |
2 | HG03654.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.637+3059_637+3060i others(13): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641225 | ||||||
| chr5:10641225 | C | CTTTT | 7 | a0001c0001t0006g0024 a0003c0016t0001g0006 a0003c0016t0001g0010 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+3077_637+3080d others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641225 | ||||||
| chr5:10641225 | CT | C | 9 | a0001c0001t0001g0156 a0001c0001t0001g0310 a0001c0001t0005g0052 others(6): Show |
9 | HG00609.hp2 HG01069.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+3080delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641225 | ||||||
| chr5:10641227 | T | TCTTC | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+3059_637+3060i others(6): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641227 | |||||||
| chr5:10641227 | T | TCTTCTTC others(3): Show |
2 | a0001c0002t0001g0164 a0001c0002t0001g0181 |
2 | HG02074.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.637+3059_637+3060i others(12): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641227 | |||||||
| chr5:10641229 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.637+3061T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641229 | |||||||
| chr5:10641267 | C | T | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.637+3099C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641267 | |||||||
| chr5:10641385 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+3217C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641385 | |||||||
| chr5:10641446 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.637+3278C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641446 | |||||||
| chr5:10641494 | T | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+3326T>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641494 | |||||||
| chr5:10641684 | A | T | 1 | a0001c0003t0003g0212 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.637+3516A>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641684 | |||||||
| chr5:10641744 | A | G | 16 | a0001c0002t0001g0137 a0001c0002t0001g0147 a0001c0002t0001g0148 others(13): Show |
16 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+3576A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641744 | |||||||
| chr5:10641801 | TAAA | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+3642_637+3644d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10641801 | ||||||
| chr5:10641867 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+3699T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641867 | |||||||
| chr5:10641880 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+3712C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641880 | |||||||
| chr5:10641889 | A | G | 2 | a0001c0001t0026g0167 a0001c0001t0026g0210 |
2 | NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.637+3721A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10641889 | |||||||
| chr5:10642057 | A | G | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+3889A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642057 | |||||||
| chr5:10642149 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+3981G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642149 | |||||||
| chr5:10642260 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637+4092T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642260 | |||||||
| chr5:10642325 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4157A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642325 | |||||||
| chr5:10642488 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4320A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642488 | |||||||
| chr5:10642618 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4450T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642618 | |||||||
| chr5:10642626 | G | C | 11 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+4458G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642626 | |||||||
| chr5:10642636 | C | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4468C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642636 | |||||||
| chr5:10642686 | C | T | 2 | a0001c0001t0005g0229 a0001c0001t0048g0117 |
2 | HG02083.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.637+4518C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642686 | |||||||
| chr5:10642775 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4607C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642775 | |||||||
| chr5:10642827 | C | T | 2 | a0001c0001t0006g0296 a0001c0001t0006g0297 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.637+4659C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642827 | |||||||
| chr5:10642904 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4736C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642904 | |||||||
| chr5:10642927 | C | T | 7 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0004c0008t0010g0074 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+4759C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642927 | |||||||
| chr5:10642928 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+4760G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10642928 | |||||||
| chr5:10643009 | A | G | 6 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(3): Show |
6 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+4841A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643009 | |||||||
| chr5:10643038 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+4870A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643038 | |||||||
| chr5:10643070 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.637+4902A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643070 | |||||||
| chr5:10643353 | A | G | 1 | a0001c0003t0007g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.637+5185A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643353 | |||||||
| chr5:10643432 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.637+5264T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643432 | |||||||
| chr5:10643437 | G | A | 1 | a0001c0001t0005g0050 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.637+5269G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643437 | |||||||
| chr5:10643466 | AT | A | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0195 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+5302delT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10643466 | ||||||
| chr5:10643587 | G | A | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.637+5419G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643587 | |||||||
| chr5:10643602 | G | A | 97 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(94): Show |
97 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.637+5434G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643602 | |||||||
| chr5:10643735 | G | C | 1 | a0001c0002t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.638-5531G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643735 | |||||||
| chr5:10643784 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-5482T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643784 | |||||||
| chr5:10643819 | C | CA | 72 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0062 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.638-5425dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10643819 | ||||||
| chr5:10643819 | CA | C | 8 | a0001c0001t0001g0219 a0001c0001t0004g0092 a0001c0001t0006g0013 others(5): Show |
8 | HG02155.hp1 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-5425delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10643819 | ||||||
| chr5:10643819 | CAA | C | 9 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0003t0003g0053 others(6): Show |
9 | HG01358.hp1 HG01361.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.638-5426_638-5425d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10643819 | ||||||
| chr5:10643819 | CAAA | C | 92 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(89): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.638-5427_638-5425d others(5): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10643819 | ||||||
| chr5:10643835 | A | G | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.638-5431A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643835 | |||||||
| chr5:10643911 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-5355C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643911 | |||||||
| chr5:10643971 | T | C | 103 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(100): Show |
103 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.638-5295T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643971 | |||||||
| chr5:10643996 | G | A | 2 | a0001c0001t0001g0305 a0001c0011t0001g0001 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.638-5270G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10643996 | |||||||
| chr5:10644005 | T | TA | 7 | a0001c0001t0001g0032 a0001c0001t0001g0240 a0001c0001t0004g0090 others(4): Show |
7 | HG01243.hp1 HG02080.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.638-5245dupA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10644005 | ||||||
| chr5:10644005 | T | TAA | 11 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0002c0010t0015g0026 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.638-5246_638-5245d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10644005 | ||||||
| chr5:10644005 | TA | T | 125 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0273 others(122): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.638-5245delA | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10644005 | ||||||
| chr5:10644019 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-5247A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644019 | |||||||
| chr5:10644228 | C | G | 1 | a0001c0001t0004g0092 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.638-5038C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644228 | |||||||
| chr5:10644265 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-5001G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644265 | |||||||
| chr5:10644276 | T | C | 1 | a0001c0004t0002g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.638-4990T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644276 | |||||||
| chr5:10644518 | A | G | 1 | a0001c0004t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.638-4748A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644518 | |||||||
| chr5:10644533 | C | T | 1 | a0001c0005t0002g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.638-4733C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644533 | |||||||
| chr5:10644556 | C | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4710C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644556 | |||||||
| chr5:10644606 | G | A | 118 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(115): Show |
118 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.638-4660G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644606 | |||||||
| chr5:10644621 | G | A | 64 | a0001c0002t0001g0040 a0001c0002t0001g0063 a0001c0002t0001g0064 others(61): Show |
64 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.638-4645G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644621 | |||||||
| chr5:10644694 | C | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4572C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644694 | |||||||
| chr5:10644867 | AG | A | 4 | a0001c0002t0006g0322 a0005c0017t0020g0136 a0005c0017t0021g0127 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-4397delG | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10644867 | ||||||
| chr5:10644872 | G | A | 1 | a0001c0003t0003g0225 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.638-4394G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644872 | |||||||
| chr5:10644887 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4379A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644887 | |||||||
| chr5:10644945 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.638-4321C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644945 | |||||||
| chr5:10644948 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4318G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644948 | |||||||
| chr5:10644964 | C | T | 1 | a0009c0032t0003g0270 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.638-4302C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10644964 | |||||||
| chr5:10645031 | C | T | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.638-4235C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645031 | |||||||
| chr5:10645091 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4175T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645091 | |||||||
| chr5:10645092 | G | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4174G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645092 | |||||||
| chr5:10645114 | T | C | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-4152T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645114 | |||||||
| chr5:10645298 | A | G | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-3968A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645298 | |||||||
| chr5:10645452 | A | AT | 15 | a0001c0002t0001g0137 a0001c0002t0001g0147 a0001c0002t0001g0148 others(12): Show |
15 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.638-3805dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10645452 | ||||||
| chr5:10645541 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.638-3725C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645541 | |||||||
| chr5:10645694 | A | C | 131 | a0001c0001t0001g0076 a0001c0001t0006g0024 a0001c0002t0001g0040 others(128): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.638-3572A>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645694 | |||||||
| chr5:10645759 | C | T | 119 | a0001c0002t0001g0040 a0001c0002t0001g0045 a0001c0002t0001g0063 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.638-3507C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10645759 | |||||||
| chr5:10646085 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.638-3181C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10646085 | |||||||
| chr5:10646093 | A | G | 112 | a0001c0002t0001g0045 a0001c0002t0001g0063 a0001c0002t0001g0064 others(109): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.638-3173A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10646093 | |||||||
| chr5:10646271 | C | T | 7 | a0001c0002t0004g0107 a0001c0002t0027g0070 a0001c0009t0008g0289 others(4): Show |
7 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.638-2995C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10646271 | |||||||
| chr5:10646513 | G | A | 2 | a0001c0001t0006g0286 a0001c0006t0058g0023 |
2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.638-2753G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10646513 | |||||||
| chr5:10646693 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0031g0082 |
2 | HG02056.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.638-2573A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10646693 | |||||||
| chr5:10646943 | G | A | 98 | a0001c0001t0001g0027 a0001c0001t0001g0129 a0001c0001t0001g0178 others(95): Show |
98 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.638-2323G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10646943 | |||||||
| chr5:10647001 | G | A | 1 | a0001c0001t0059g0021 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-2265G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647001 | |||||||
| chr5:10647005 | G | C | 2 | a0001c0004t0002g0058 a0001c0004t0002g0298 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.638-2261G>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647005 | |||||||
| chr5:10647025 | A | G | 8 | a0001c0004t0002g0123 a0001c0004t0002g0139 a0001c0004t0002g0141 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-2241A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647025 | |||||||
| chr5:10647109 | A | AT | 41 | a0001c0001t0013g0035 a0001c0001t0013g0196 a0001c0001t0013g0197 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.638-2144dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10647109 | ||||||
| chr5:10647110 | T | A | 1 | a0002c0012t0015g0285 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-2156T>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647110 | |||||||
| chr5:10647174 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.638-2092G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647174 | |||||||
| chr5:10647262 | G | A | 1 | a0001c0002t0004g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.638-2004G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647262 | |||||||
| chr5:10647322 | T | C | 101 | a0001c0001t0001g0300 a0001c0001t0013g0035 a0001c0001t0013g0196 others(98): Show |
101 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.638-1944T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647322 | |||||||
| chr5:10647325 | G | T | 1 | a0001c0030t0019g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.638-1941G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647325 | |||||||
| chr5:10647467 | A | G | 1 | a0001c0002t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.638-1799A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647467 | |||||||
| chr5:10647607 | C | CT | 24 | a0001c0001t0013g0035 a0001c0001t0013g0196 a0001c0001t0013g0197 others(21): Show |
24 | HG00408.hp1 HG00544.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.638-1658dupT | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10647607 | ||||||
| chr5:10647839 | C | A | 5 | a0004c0008t0010g0074 a0004c0008t0010g0075 a0004c0008t0010g0292 others(2): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-1427C>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647839 | |||||||
| chr5:10647937 | T | C | 1 | a0002c0028t0037g0007 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.638-1329T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10647937 | |||||||
| chr5:10648000 | A | G | 2 | a0001c0001t0051g0315 a0008c0036t0001g0047 |
2 | NA18950.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.638-1266A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648000 | |||||||
| chr5:10648042 | A | G | 5 | a0004c0008t0010g0074 a0004c0008t0010g0075 a0004c0008t0010g0292 others(2): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-1224A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648042 | |||||||
| chr5:10648161 | C | CGT | 99 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0054 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.638-1102_638-1101d others(4): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10648161 | ||||||
| chr5:10648212 | G | T | 38 | a0001c0004t0002g0042 a0001c0004t0002g0058 a0001c0004t0002g0123 others(35): Show |
38 | HG00642.hp1 HG00642.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.638-1054G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648212 | |||||||
| chr5:10648245 | C | T | 1 | a0001c0005t0002g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.638-1021C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648245 | |||||||
| chr5:10648260 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.638-1006G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648260 | |||||||
| chr5:10648551 | G | T | 2 | a0006c0018t0035g0112 a0006c0018t0061g0087 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.638-715G>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648551 | |||||||
| chr5:10648563 | T | C | 97 | a0001c0003t0003g0036 a0001c0003t0003g0053 a0001c0003t0003g0056 others(94): Show |
97 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.638-703T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648563 | |||||||
| chr5:10648570 | A | G | 16 | a0001c0003t0007g0213 a0001c0003t0007g0215 a0001c0003t0007g0254 others(13): Show |
16 | HG00639.hp2 HG02683.hp2 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-696A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648570 | |||||||
| chr5:10648605 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.638-661C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648605 | |||||||
| chr5:10648673 | C | G | 16 | a0001c0003t0007g0213 a0001c0003t0007g0215 a0001c0003t0007g0254 others(13): Show |
16 | HG00639.hp2 HG02683.hp2 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-593C>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648673 | |||||||
| chr5:10648713 | T | C | 96 | a0001c0003t0003g0036 a0001c0003t0003g0053 a0001c0003t0003g0056 others(93): Show |
96 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.638-553T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648713 | |||||||
| chr5:10648904 | G | A | 1 | a0001c0006t0058g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.638-362G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10648904 | |||||||
| chr5:10649013 | T | C | 96 | a0001c0003t0003g0036 a0001c0003t0003g0053 a0001c0003t0003g0056 others(93): Show |
96 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.638-253T>C | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10649013 | |||||||
| chr5:10649045 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.638-221C>T | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10649045 | |||||||
| chr5:10649062 | G | A | 1 | a0002c0012t0034g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.638-204G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10649062 | |||||||
| chr5:10649087 | CCGCCTTC others(3): Show |
C | 41 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0115 others(38): Show |
41 | HG00438.hp1 HG00438.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.638-175_638-166del others(10): Show |
ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 10649087 | ||||||
| chr5:10649170 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.638-96G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10649170 | |||||||
| chr5:10649175 | G | A | 1 | a0002c0012t0034g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.638-91G>A | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10649175 | |||||||
| chr5:10649180 | A | G | 5 | a0001c0009t0008g0289 a0001c0009t0008g0304 a0001c0009t0008g0313 others(2): Show |
5 | HG01361.hp1 HG01884.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-86A>G | ANKRD33B | ENSG00000164236.12 | transcript | ENST00000296657.7 | protein_coding | 3/3 | chr5 | 10649180 |