Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 255967 |
| ensemblid | ENSG00000152520.14 |
| hgncid | 29991 |
| symbol | PAN3 |
| name | poly(A) specific ribonuclease subunit PAN3 |
| refseq_nuc | NM_175854.8 |
| refseq_prot | NP_787050.6 |
| ensembl_nuc | ENST00000380958.8 |
| ensembl_prot | ENSP00000370345.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 28138545 |
| end | 28295335 |
| strand | + |
| ver | v1.2 |
| region | chr13:28138545-28295335 |
| region5000 | chr13:28133545-28300335 |
| regionname0 | PAN3_chr13_28138545_28295335 |
| regionname5000 | PAN3_chr13_28133545_28300335 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 887 | 250 | 79 | 34 | 108 | 2 | 25 | 80 | PAN3_chr13_28133545_28300335 | PAN3 | MNSGG others(882): Show |
chr13 | 28133545 | 28300335 |
| a0002 | 0/0 | 887 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | MNSGG others(882): Show |
chr13 | 28133545 | 28300335 |
| a0003 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | MNSGG others(882): Show |
chr13 | 28133545 | 28300335 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2661 | 238 | 71 | 31 | 107 | 2 | 25 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0001c0002 | 0/0 | 2661 | 5 | 4 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0001c0003 | 0/0 | 2661 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0001c0004 | 0/0 | 2661 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0001c0007 | 0/0 | 2661 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0001c0008 | 0/0 | 2661 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0001c0009 | 0/0 | 2661 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0002c0005 | 0/0 | 2661 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 | ||
| a0003c0006 | 0/0 | 2661 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ATGAA others(2656): Show |
chr13 | 28133545 | 28300335 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5586 | 69 | 13 | 6 | 39 | 0 | 11 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0002 | 0/0 | 5606 | 33 | 3 | 1 | 28 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5601): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0003 | 0/0 | 5607 | 21 | 7 | 4 | 10 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5602): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0004 | 0/1 | 5587 | 18 | 1 | 4 | 9 | 0 | 3 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0005 | 0/0 | 5600 | 12 | 4 | 2 | 3 | 1 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0006 | 0/0 | 5590 | 9 | 2 | 5 | 0 | 0 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5585): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0007 | 0/0 | 5601 | 7 | 1 | 2 | 2 | 0 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5596): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0008 | 0/0 | 5599 | 6 | 5 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0009 | 0/0 | 5605 | 6 | 2 | 0 | 4 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5600): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0010 | 0/0 | 5597 | 5 | 5 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5592): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0011 | 0/0 | 5599 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0013 | 0/0 | 5586 | 3 | 2 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0014 | 0/0 | 5590 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5585): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0015 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5596): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0016 | 0/0 | 5597 | 2 | 0 | 0 | 1 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5592): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0017 | 0/0 | 5599 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0019 | 0/0 | 5600 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0020 | 0/0 | 5596 | 2 | 0 | 0 | 2 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5591): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0022 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5603): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0023 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0024 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5596): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0025 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5596): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0026 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5590): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0027 | 0/0 | 5598 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5593): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0028 | 0/0 | 5598 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5593): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0029 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0030 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0031 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5603): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0032 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0033 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5606): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0034 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5600): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0035 | 0/0 | 5606 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5601): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0036 | 0/0 | 5598 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5593): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0037 | 0/0 | 5608 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5603): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0038 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5615): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0039 | 0/0 | 5598 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5593): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0040 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0041 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0042 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0043 | 0/0 | 5590 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5585): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0044 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0045 | 0/0 | 5590 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5585): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0046 | 0/0 | 5586 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0047 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5607): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0048 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0049 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5590): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0050 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0051 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0052 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0053 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0054 | 1/0 | 5590 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5585): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0055 | 0/0 | 5586 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0001t0056 | 0/0 | 5587 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0002t0012 | 0/0 | 5600 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5595): Show |
chr13 | 28133545 | 28300335 |
| a0001c0002t0018 | 0/0 | 5599 | 2 | 1 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5594): Show |
chr13 | 28133545 | 28300335 |
| a0001c0003t0001 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0003t0004 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0003t0014 | 0/0 | 5590 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5585): Show |
chr13 | 28133545 | 28300335 |
| a0001c0004t0004 | 0/0 | 5587 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5582): Show |
chr13 | 28133545 | 28300335 |
| a0001c0007t0021 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5606): Show |
chr13 | 28133545 | 28300335 |
| a0001c0008t0001 | 0/0 | 5586 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0001c0009t0001 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0002c0005t0001 | 0/0 | 5586 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5581): Show |
chr13 | 28133545 | 28300335 |
| a0003c0006t0015 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | ACCCG others(5596): Show |
chr13 | 28133545 | 28300335 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0013g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0014g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0014g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0017g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0017g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0020g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0022g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0023g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0024g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0025g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0026g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0027g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0028g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0029g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0030g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0031g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0032g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0033g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0034g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0035g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0036g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0037g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0038g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0039g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0040g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0041g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0042g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0043g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0044g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0045g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0046g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0047g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0048g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0049g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0050g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0051g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0052g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0053g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0054g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0055g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0056g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0018g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0003t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0003t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0004t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0007t0021g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0008t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0002c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0003c0006t0015g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0176 | EUR | GBR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00099 | hp2 | a0001 | c0001 | t0013 | g0016 | EUR | GBR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0206 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00735 | hp2 | a0001 | c0001 | t0026 | g0239 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0132 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01099 | hp1 | a0001 | c0001 | t0027 | g0150 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01109 | hp1 | a0001 | c0002 | t0018 | g0212 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0177 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01175 | hp2 | a0001 | c0001 | t0056 | g0063 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01346 | hp2 | a0001 | c0001 | t0045 | g0051 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01358 | hp2 | a0001 | c0001 | t0025 | g0203 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01361 | hp1 | a0001 | c0001 | t0022 | g0226 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01361 | hp2 | a0001 | c0004 | t0004 | g0065 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0178 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0247 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0124 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02004 | hp2 | a0001 | c0008 | t0001 | g0069 | AMR | PEL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02040 | hp2 | a0001 | c0001 | t0053 | g0046 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0218 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02132 | hp1 | a0001 | c0001 | t0050 | g0050 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02135 | hp2 | a0001 | c0001 | t0051 | g0099 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02145 | hp1 | a0001 | c0001 | t0024 | g0228 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02165 | hp2 | a0001 | c0001 | t0034 | g0190 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0113 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02257 | hp2 | a0001 | c0001 | t0041 | g0006 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0204 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02258 | hp2 | a0001 | c0001 | t0038 | g0243 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0205 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02572 | hp2 | a0001 | c0001 | t0042 | g0186 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02602 | hp1 | a0001 | c0001 | t0043 | g0252 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02602 | hp2 | a0002 | c0005 | t0001 | g0131 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02615 | hp2 | a0001 | c0001 | t0047 | g0023 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02717 | hp1 | a0001 | c0001 | t0032 | g0227 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02723 | hp2 | a0001 | c0001 | t0039 | g0005 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02809 | hp2 | a0001 | c0001 | t0030 | g0161 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0238 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0121 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0245 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02922 | hp1 | a0001 | c0003 | t0014 | g0084 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02965 | hp2 | a0001 | c0007 | t0021 | g0151 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02970 | hp2 | a0001 | c0002 | t0012 | g0211 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03017 | hp1 | a0001 | c0001 | t0016 | g0195 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0248 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03098 | hp1 | a0001 | c0001 | t0029 | g0249 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03098 | hp2 | a0001 | c0001 | t0031 | g0223 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0187 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0123 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0128 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0189 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0019 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03453 | hp1 | a0001 | c0002 | t0012 | g0162 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03453 | hp2 | a0001 | c0001 | t0023 | g0171 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03486 | hp1 | a0001 | c0001 | t0048 | g0022 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03486 | hp2 | a0001 | c0001 | t0040 | g0004 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03516 | hp1 | a0003 | c0006 | t0015 | g0251 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03516 | hp2 | a0001 | c0002 | t0012 | g0209 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0126 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0136 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0182 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0116 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0053 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0180 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0082 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04228 | hp1 | a0001 | c0001 | t0055 | g0074 | SAS | STU | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04228 | hp2 | a0001 | c0001 | t0046 | g0035 | SAS | STU | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18522 | hp1 | a0001 | c0001 | t0052 | g0112 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18943 | hp2 | a0001 | c0001 | t0009 | g0192 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18956 | hp2 | a0001 | c0001 | t0016 | g0040 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0237 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18974 | hp2 | a0001 | c0001 | t0035 | g0200 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18981 | hp2 | a0001 | c0001 | t0009 | g0217 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18986 | hp2 | a0001 | c0001 | t0049 | g0154 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18993 | hp2 | a0001 | c0001 | t0044 | g0048 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18998 | hp1 | a0001 | c0001 | t0036 | g0041 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19003 | hp1 | a0001 | c0001 | t0020 | g0194 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0114 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0250 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19068 | hp2 | a0001 | c0001 | t0020 | g0202 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19078 | hp2 | a0001 | c0009 | t0001 | g0064 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19085 | hp2 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19090 | hp2 | a0001 | c0001 | t0037 | g0220 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19240 | hp1 | a0001 | c0002 | t0018 | g0210 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | GIH | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0181 | SAS | GIH | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0185 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0125 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0244 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0242 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0127 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0057 | REF | REF | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0054 | g0102 | REF | REF | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28256402 | G | A | 1 | a0002 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1111G>A | p.Val371Met | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/19 | 1224/5590 | 1111/2664 | 371/887 | chr13 | 28256402 | |||
| chr13:28270824 | G | A | 1 | a0003 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1916G>A | p.Arg639Gln | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/19 | 2029/5590 | 1916/2664 | 639/887 | chr13 | 28270824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28138834 | C | T | 1 | a0001c0009 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.177C>T | p.Phe59Phe | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 290/5590 | 177/2664 | 59/887 | chr13 | 28138834 | |||
| chr13:28138858 | G | T | 1 | a0001c0008 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.201G>T | p.Leu67Leu | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 314/5590 | 201/2664 | 67/887 | chr13 | 28138858 | |||
| chr13:28220374 | G | A | 1 | a0001c0004 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.996G>A | p.Ala332Ala | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/19 | 1109/5590 | 996/2664 | 332/887 | chr13 | 28220374 | |||
| chr13:28256299 | G | A | 1 | a0001c0003 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1008G>A | p.Ser336Ser | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/19 | 1121/5590 | 1008/2664 | 336/887 | chr13 | 28256299 | |||
| chr13:28260488 | C | T | 1 | a0001c0003 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1290C>T | p.His430His | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/19 | 1403/5590 | 1290/2664 | 430/887 | chr13 | 28260488 | |||
| chr13:28280520 | C | A | 1 | a0001c0002 | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.2298C>A | p.Val766Val | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/19 | 2411/5590 | 2298/2664 | 766/887 | chr13 | 28280520 | |||
| chr13:28281338 | T | C | 1 | a0001c0007 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.2343T>C | p.Phe781Phe | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/19 | 2456/5590 | 2343/2664 | 781/887 | chr13 | 28281338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28138552 | C | G | 1 | a0001c0001t0056 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 106 | chr13 | 28138552 | ||||||
| chr13:28138594 | C | T | 1 | a0001c0001t0055 | 1 | HG04228.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | chr13 | 28138594 | |||||||
| chr13:28138603 | T | TGGCGGCG others(2): Show |
36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(33): Show |
127 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-52insCGGCGGCG others(1): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 52 | INFO_REALIGN_3_PRIME | chr13 | 28138603 | |||||
| chr13:28138603 | T | TGGCGGCG others(5): Show |
1 | a0001c0007t0021 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53_-52insCGGCGGCG others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 52 | INFO_REALIGN_3_PRIME | chr13 | 28138603 | |||||
| chr13:28138606 | T | C | 39 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(36): Show |
131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-52T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 52 | chr13 | 28138606 | ||||||
| chr13:28292549 | T | TG | 5 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0042 others(2): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*29dupG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 30 | INFO_REALIGN_3_PRIME | chr13 | 28292549 | |||||
| chr13:28292873 | T | C | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 351 | chr13 | 28292873 | ||||||
| chr13:28292876 | T | C | 1 | a0001c0001t0044 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 354 | chr13 | 28292876 | ||||||
| chr13:28292878 | G | C | 1 | a0001c0001t0022 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*356G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 356 | chr13 | 28292878 | ||||||
| chr13:28292921 | G | A | 2 | a0001c0001t0023 a0001c0001t0024 |
2 | HG02145.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 399 | chr13 | 28292921 | ||||||
| chr13:28293005 | T | C | 1 | a0001c0001t0042 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 483 | chr13 | 28293005 | ||||||
| chr13:28293023 | C | T | 3 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0024 |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*501C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 501 | chr13 | 28293023 | ||||||
| chr13:28293043 | C | T | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
236 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 521 | chr13 | 28293043 | ||||||
| chr13:28293108 | C | T | 2 | a0001c0001t0006 a0001c0001t0045 |
10 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*586C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 586 | chr13 | 28293108 | ||||||
| chr13:28293121 | C | G | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(10): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*599C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 599 | chr13 | 28293121 | ||||||
| chr13:28293131 | C | T | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 others(15): Show |
103 | HG00438.hp1 HG01081.hp1 HG01099.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 609 | chr13 | 28293131 | ||||||
| chr13:28293387 | G | GT | 4 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0032 others(1): Show |
15 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*894dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | G | GTT | 5 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0024 others(2): Show |
11 | HG00597.hp2 HG01175.hp1 HG01358.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*893_*894dupTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0033 a0001c0001t0038 |
2 | HG02258.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*883_*894dupTTTTTT others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0047 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882_*894dupTTTTTT others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | GT | G | 7 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0027 others(4): Show |
30 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*894delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 894 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | GTT | G | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0016 others(1): Show |
41 | HG00438.hp2 HG00597.hp1 HG01261.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*893_*894delTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 893 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | GTTT | G | 10 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0020 others(7): Show |
32 | HG01109.hp2 HG01175.hp2 HG01261.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*894delTTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 892 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293387 | GTTTT | G | 12 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0026 others(9): Show |
82 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*891_*894delTTTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 891 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | |||||
| chr13:28293391 | T | TTTTTTG | 1 | a0001c0001t0008 | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*874_*875insGTTTTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 875 | INFO_REALIGN_3_PRIME | chr13 | 28293391 | |||||
| chr13:28293415 | T | G | 1 | a0001c0001t0048 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*893T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 893 | chr13 | 28293415 | ||||||
| chr13:28293416 | T | G | 1 | a0001c0001t0034 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*894T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 894 | chr13 | 28293416 | ||||||
| chr13:28293419 | G | T | 1 | a0001c0001t0032 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 897 | chr13 | 28293419 | ||||||
| chr13:28293421 | G | C | 3 | a0001c0001t0015 a0001c0001t0029 a0003c0006t0015 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*899G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 899 | chr13 | 28293421 | ||||||
| chr13:28293426 | G | A | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0027 others(1): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 904 | chr13 | 28293426 | ||||||
| chr13:28293442 | T | C | 3 | a0001c0001t0015 a0001c0001t0029 a0003c0006t0015 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*920T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 920 | chr13 | 28293442 | ||||||
| chr13:28293455 | C | T | 2 | a0001c0001t0050 a0001c0001t0051 |
2 | HG02132.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*933C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 933 | chr13 | 28293455 | ||||||
| chr13:28293581 | T | G | 1 | a0001c0001t0032 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 1059 | chr13 | 28293581 | ||||||
| chr13:28293609 | T | A | 1 | a0001c0001t0035 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 1087 | chr13 | 28293609 | ||||||
| chr13:28294156 | G | A | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0027 others(1): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1634G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 1634 | chr13 | 28294156 | ||||||
| chr13:28294750 | G | A | 2 | a0001c0002t0012 a0001c0002t0018 |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2228G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2228 | chr13 | 28294750 | ||||||
| chr13:28295010 | G | GGATATAA others(2): Show |
14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(11): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2489_*2497dupGATA others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2498 | INFO_REALIGN_3_PRIME | chr13 | 28295010 | |||||
| chr13:28295206 | A | G | 1 | a0001c0001t0046 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2684A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2684 | chr13 | 28295206 | ||||||
| chr13:28295326 | C | A | 1 | a0001c0001t0045 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2804C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2804 | chr13 | 28295326 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28139118 | G | A | 3 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 |
3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.430+31G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139118 | |||||||
| chr13:28139135 | T | A | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.430+48T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139135 | |||||||
| chr13:28139188 | C | T | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.430+101C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139188 | |||||||
| chr13:28139225 | C | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.430+138C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139225 | |||||||
| chr13:28139505 | GGGGT | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+420_430+423del others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139505 | ||||||
| chr13:28139507 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+426_430+427ins others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139507 | ||||||
| chr13:28139514 | T | G | 4 | a0001c0001t0008g0007 a0001c0001t0015g0250 a0001c0001t0029g0249 others(1): Show |
4 | HG03098.hp1 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+427T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139514 | |||||||
| chr13:28139514 | T | TTG | 32 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0129 others(29): Show |
32 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.430+463_430+464dup others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTG | 12 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.430+461_430+464dup others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTG | 28 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0001t0002g0167 others(25): Show |
28 | HG00099.hp1 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.430+459_430+464dup others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(1): Show |
25 | a0001c0001t0001g0213 a0001c0001t0002g0191 a0001c0001t0002g0193 others(22): Show |
25 | HG00597.hp2 HG00639.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+457_430+464dup others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(3): Show |
19 | a0001c0001t0002g0216 a0001c0001t0002g0219 a0001c0001t0002g0222 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+455_430+464dup others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(5): Show |
11 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0235 others(8): Show |
11 | HG01261.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+453_430+464dup others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(7): Show |
4 | a0001c0001t0002g0240 a0001c0001t0003g0241 a0001c0001t0011g0242 others(1): Show |
4 | HG00735.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+451_430+464dup others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0008g0244 a0001c0001t0038g0243 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.430+449_430+464dup others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(13): Show |
2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430+445_430+464dup others(20): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(15): Show |
1 | a0001c0001t0008g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430+443_430+464dup others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | T | TTGTGTGT others(19): Show |
1 | a0001c0001t0008g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.430+439_430+464dup others(26): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | TTG | T | 30 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(27): Show |
30 | HG00099.hp2 HG00735.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.430+463_430+464del others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139514 | TTGTGTG | T | 5 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0003g0008 others(2): Show |
5 | HG02083.hp1 NA18961.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+459_430+464del others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | ||||||
| chr13:28139824 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+737A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139824 | |||||||
| chr13:28139845 | G | A | 2 | a0001c0001t0026g0239 a0001c0007t0021g0151 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+758G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139845 | |||||||
| chr13:28139936 | G | GTGT | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0004g0043 others(1): Show |
4 | HG02015.hp1 HG03453.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+875_430+877dup others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139936 | ||||||
| chr13:28139936 | GTGT | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0213 a0001c0007t0021g0151 |
3 | HG02015.hp2 HG02965.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.430+875_430+877del others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139936 | ||||||
| chr13:28140022 | A | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+935A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140022 | |||||||
| chr13:28140305 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.430+1218A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140305 | |||||||
| chr13:28140410 | AAAATAAT others(3): Show |
A | 3 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 |
3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430+1325_430+1334d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28140410 | ||||||
| chr13:28140413 | A | G | 2 | a0001c0001t0002g0225 a0001c0001t0022g0226 |
2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.430+1326A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140413 | |||||||
| chr13:28140417 | T | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+1330T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140417 | |||||||
| chr13:28140540 | G | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.430+1453G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140540 | |||||||
| chr13:28140672 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+1585A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140672 | |||||||
| chr13:28140687 | T | TTGTTC | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1612_430+1616d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28140687 | ||||||
| chr13:28140699 | G | GTTCTT | 125 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(122): Show |
125 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.430+1617_430+1621d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28140699 | ||||||
| chr13:28140718 | C | T | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430+1631C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140718 | |||||||
| chr13:28140881 | A | G | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1794A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140881 | |||||||
| chr13:28140883 | C | T | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1796C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140883 | |||||||
| chr13:28140909 | G | C | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+1822G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140909 | |||||||
| chr13:28140983 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0014g0113 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1896C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140983 | |||||||
| chr13:28141003 | C | CT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG02055.hp2 HG03017.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+1935dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | C | CTTTTTAT others(1): Show |
5 | a0001c0001t0002g0225 a0001c0001t0003g0001 a0001c0001t0003g0224 others(2): Show |
5 | HG01361.hp1 HG02622.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1921_430+1922i others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | C | CTTTTTT | 9 | a0001c0001t0008g0245 a0001c0001t0023g0171 a0001c0001t0026g0239 others(6): Show |
9 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+1930_430+1935d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | C | CTTTTTTT | 27 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(24): Show |
27 | HG01099.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.430+1929_430+1935d others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0005g0176 a0001c0001t0005g0188 a0001c0001t0007g0177 others(5): Show |
8 | HG00099.hp1 HG00639.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1928_430+1935d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | C | CTTTTTTT others(2): Show |
14 | a0001c0001t0005g0179 a0001c0001t0005g0181 a0001c0001t0005g0182 others(11): Show |
14 | HG00597.hp2 HG00639.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.430+1927_430+1935d others(11): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0005g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430+1926_430+1935d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141003 | CT | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0006g0013 others(3): Show |
6 | HG01069.hp1 HG02040.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+1935delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | ||||||
| chr13:28141006 | T | TTTATTTT others(1): Show |
9 | a0001c0001t0002g0002 a0001c0001t0002g0233 a0001c0001t0002g0240 others(6): Show |
9 | HG01167.hp2 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1921_430+1922i others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141006 | ||||||
| chr13:28141007 | T | TTATTTTT others(1): Show |
55 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(52): Show |
55 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.430+1921_430+1922i others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141007 | ||||||
| chr13:28141067 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.430+1980G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141067 | |||||||
| chr13:28141379 | C | T | 70 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(67): Show |
70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.430+2292C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141379 | |||||||
| chr13:28141379 | CTT | C | 4 | a0001c0001t0005g0179 a0001c0001t0005g0206 a0001c0001t0007g0178 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2295_430+2296d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141379 | ||||||
| chr13:28141456 | TTTTTTC | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+2375_430+2380d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141456 | ||||||
| chr13:28141462 | C | CT | 35 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0070 others(32): Show |
35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.430+2397dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | ||||||
| chr13:28141462 | C | CTT | 10 | a0001c0001t0002g0168 a0001c0001t0002g0235 a0001c0001t0005g0207 others(7): Show |
10 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.430+2396_430+2397d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | ||||||
| chr13:28141462 | CT | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0002g0197 others(5): Show |
8 | HG01099.hp2 HG01167.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+2397delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | ||||||
| chr13:28141462 | CTTTTT | C | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+2393_430+2397d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | ||||||
| chr13:28141462 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430+2384_430+2397d others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | ||||||
| chr13:28141468 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0013g0127 a0001c0001t0013g0128 |
3 | HG03017.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.430+2381T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141468 | |||||||
| chr13:28141542 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+2455A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141542 | |||||||
| chr13:28141702 | G | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0001g0130 others(15): Show |
18 | HG00099.hp2 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+2615G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141702 | |||||||
| chr13:28141703 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0004g0055 |
2 | HG02165.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.430+2616G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141703 | |||||||
| chr13:28141791 | A | T | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.430+2704A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141791 | |||||||
| chr13:28141793 | G | C | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2706G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141793 | |||||||
| chr13:28141806 | A | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+2719A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141806 | |||||||
| chr13:28142027 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.430+2940A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142027 | |||||||
| chr13:28142325 | G | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+3238G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142325 | |||||||
| chr13:28142334 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+3247C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142334 | |||||||
| chr13:28142481 | A | ATGTGTGT others(3): Show |
5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0014g0113 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+3395_430+3404d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142481 | ||||||
| chr13:28142511 | A | AT | 7 | a0001c0001t0001g0033 a0001c0001t0001g0105 a0001c0001t0001g0119 others(4): Show |
7 | HG01071.hp2 HG02015.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+3443dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTT | 6 | a0001c0001t0002g0143 a0001c0001t0003g0142 a0001c0001t0017g0204 others(3): Show |
6 | HG01069.hp2 HG01358.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+3439_430+3443d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTT | 51 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0036 others(48): Show |
51 | HG00438.hp2 HG00597.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.430+3438_430+3443d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT | 11 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0201 others(8): Show |
11 | HG02135.hp1 HG02895.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+3437_430+3443d others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(1): Show |
8 | a0001c0001t0002g0225 a0001c0001t0003g0001 a0001c0001t0003g0229 others(5): Show |
8 | HG01361.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+3436_430+3443d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0002g0233 a0001c0001t0002g0240 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.430+3434_430+3443d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0008g0244 a0001c0001t0008g0248 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.430+3433_430+3443d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+3432_430+3443d others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0008g0245 a0001c0001t0008g0246 a0001c0001t0008g0247 |
3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430+3431_430+3443d others(15): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0010g0152 a0001c0001t0033g0123 |
2 | HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.430+3430_430+3443d others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0010g0121 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.430+3429_430+3443d others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0010g0122 a0001c0001t0028g0125 |
2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.430+3428_430+3443d others(18): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0010g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+3427_430+3443d others(19): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0010g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430+3425_430+3443d others(21): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | AT | A | 8 | a0001c0001t0001g0056 a0001c0001t0003g0141 a0001c0001t0005g0172 others(5): Show |
8 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+3443delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142511 | ATT | A | 27 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(24): Show |
27 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.430+3442_430+3443d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | ||||||
| chr13:28142558 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+3471C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142558 | |||||||
| chr13:28142567 | C | G | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+3480C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142567 | |||||||
| chr13:28142612 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+3525C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142612 | |||||||
| chr13:28142774 | G | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+3687G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142774 | |||||||
| chr13:28142978 | G | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0140 a0001c0001t0004g0104 |
3 | NA18948.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.430+3891G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142978 | |||||||
| chr13:28143114 | G | T | 2 | a0001c0001t0026g0239 a0001c0007t0021g0151 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+4027G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143114 | |||||||
| chr13:28143120 | G | T | 25 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(22): Show |
25 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+4033G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143120 | |||||||
| chr13:28143173 | C | G | 1 | a0001c0001t0033g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.430+4086C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143173 | |||||||
| chr13:28143255 | G | T | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+4168G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143255 | |||||||
| chr13:28143379 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+4292A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143379 | |||||||
| chr13:28143483 | T | A | 1 | a0001c0001t0002g0144 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.430+4396T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143483 | |||||||
| chr13:28143533 | G | A | 2 | a0001c0001t0006g0014 a0001c0001t0045g0051 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.430+4446G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143533 | |||||||
| chr13:28143546 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(1): Show |
4 | HG02602.hp2 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+4459T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143546 | |||||||
| chr13:28143832 | C | T | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+4745C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143832 | |||||||
| chr13:28143874 | G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.430+4787G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143874 | |||||||
| chr13:28144027 | T | C | 249 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.430+4940T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144027 | |||||||
| chr13:28144160 | G | C | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.430+5073G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144160 | |||||||
| chr13:28144203 | GTTTTTTT others(4): Show |
G | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.430+5124_430+5134d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144203 | ||||||
| chr13:28144209 | TTG | T | 5 | a0001c0001t0008g0007 a0001c0001t0008g0245 a0001c0001t0008g0246 others(2): Show |
5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+5124_430+5125d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144209 | ||||||
| chr13:28144210 | TG | T | 4 | a0001c0001t0008g0244 a0001c0001t0025g0203 a0001c0001t0026g0239 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+5124delG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144210 | |||||||
| chr13:28144211 | G | GT | 45 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0081 others(42): Show |
45 | HG00438.hp1 HG00597.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.430+5147dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144211 | ||||||
| chr13:28144211 | G | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0003g0232 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5124G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144211 | |||||||
| chr13:28144211 | GT | G | 40 | a0001c0001t0002g0164 a0001c0001t0005g0172 a0001c0001t0005g0173 others(37): Show |
40 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.430+5147delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144211 | ||||||
| chr13:28144217 | T | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+5130T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144217 | |||||||
| chr13:28144219 | T | G | 1 | a0001c0001t0006g0015 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.430+5132T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144219 | |||||||
| chr13:28144220 | T | G | 6 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+5133T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144220 | |||||||
| chr13:28144222 | T | G | 2 | a0001c0001t0002g0042 a0001c0001t0007g0237 |
2 | NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.430+5135T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144222 | |||||||
| chr13:28144223 | T | G | 31 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(28): Show |
31 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.430+5136T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144223 | |||||||
| chr13:28144235 | G | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5148G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144235 | |||||||
| chr13:28144416 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+5329C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144416 | |||||||
| chr13:28144437 | A | G | 131 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(128): Show |
131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.430+5350A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144437 | |||||||
| chr13:28144438 | A | T | 1 | a0001c0001t0002g0144 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.430+5351A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144438 | |||||||
| chr13:28144514 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5427C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144514 | |||||||
| chr13:28144520 | C | T | 3 | a0001c0001t0011g0187 a0001c0001t0011g0242 a0001c0001t0019g0238 |
3 | HG02886.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.430+5433C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144520 | |||||||
| chr13:28144522 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5435A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144522 | |||||||
| chr13:28144717 | T | TC | 155 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.430+5631dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144717 | ||||||
| chr13:28144718 | C | CCT | 81 | a0001c0001t0001g0033 a0001c0001t0001g0101 a0001c0001t0001g0156 others(78): Show |
81 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.430+5631_430+5632i others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144718 | |||||||
| chr13:28144718 | C | CCTT | 6 | a0001c0001t0002g0012 a0001c0001t0002g0170 a0001c0001t0002g0222 others(3): Show |
6 | HG00438.hp2 NA18974.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+5631_430+5632i others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144718 | |||||||
| chr13:28144718 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0006g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.430+5641_430+5652d others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144718 | ||||||
| chr13:28144719 | T | C | 2 | a0001c0001t0031g0223 a0001c0001t0053g0046 |
2 | HG02040.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.430+5632T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144719 | |||||||
| chr13:28144723 | T | C | 2 | a0001c0001t0010g0124 a0001c0001t0028g0125 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.430+5636T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144723 | |||||||
| chr13:28144731 | T | C | 1 | a0001c0001t0006g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.430+5644T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144731 | |||||||
| chr13:28144739 | T | C | 3 | a0001c0001t0026g0239 a0001c0001t0031g0223 a0001c0007t0021g0151 |
3 | HG00735.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.430+5652T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144739 | |||||||
| chr13:28144839 | G | GC | 130 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(127): Show |
130 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.430+5753dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144839 | ||||||
| chr13:28144841 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.430+5754T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144841 | |||||||
| chr13:28144842 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.430+5755C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144842 | |||||||
| chr13:28144856 | A | G | 2 | a0001c0001t0050g0050 a0001c0001t0051g0099 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.430+5769A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144856 | |||||||
| chr13:28144909 | G | A | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.430+5822G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144909 | |||||||
| chr13:28145008 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0050g0050 a0001c0001t0051g0099 |
3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.430+5921G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145008 | |||||||
| chr13:28145009 | C | T | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.430+5922C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145009 | |||||||
| chr13:28145051 | T | C | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+5964T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145051 | |||||||
| chr13:28145055 | T | C | 1 | a0001c0001t0023g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.430+5968T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145055 | |||||||
| chr13:28145112 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+6025G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145112 | |||||||
| chr13:28145234 | C | T | 1 | a0001c0001t0005g0183 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.430+6147C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145234 | |||||||
| chr13:28145252 | C | CGT | 13 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(10): Show |
13 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+6176_430+6177d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145252 | ||||||
| chr13:28145252 | C | CGTGT | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+6174_430+6177d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145252 | ||||||
| chr13:28145265 | A | G | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.430+6178A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145265 | |||||||
| chr13:28145361 | A | G | 1 | a0001c0001t0011g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.430+6274A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145361 | |||||||
| chr13:28145411 | G | A | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+6324G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145411 | |||||||
| chr13:28145428 | A | G | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+6341A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145428 | |||||||
| chr13:28145449 | T | C | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.430+6362T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145449 | |||||||
| chr13:28145690 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+6603A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145690 | |||||||
| chr13:28145757 | A | AT | 24 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0002g0144 others(21): Show |
24 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.430+6692dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145757 | ||||||
| chr13:28145757 | AT | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG01099.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.430+6692delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145757 | ||||||
| chr13:28145770 | T | G | 1 | a0001c0001t0003g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430+6683T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145770 | |||||||
| chr13:28145908 | A | AGG | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+6822_430+6823d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145908 | ||||||
| chr13:28146088 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+7001C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146088 | |||||||
| chr13:28146157 | T | C | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+7070T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146157 | |||||||
| chr13:28146300 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.430+7213G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146300 | |||||||
| chr13:28146300 | G | GTC | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0096 others(17): Show |
20 | HG00639.hp2 HG01071.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.430+7238_430+7239d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28146300 | ||||||
| chr13:28146300 | G | GTCTC | 88 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
88 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.430+7236_430+7239d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28146300 | ||||||
| chr13:28146300 | GTC | G | 15 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(12): Show |
15 | HG00735.hp2 HG01099.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+7238_430+7239d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28146300 | ||||||
| chr13:28146589 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.430+7502A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146589 | |||||||
| chr13:28146650 | C | T | 4 | a0001c0001t0005g0179 a0001c0001t0005g0206 a0001c0001t0007g0178 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+7563C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146650 | |||||||
| chr13:28146703 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.430+7616C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146703 | |||||||
| chr13:28146725 | C | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+7638C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146725 | |||||||
| chr13:28146835 | C | T | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.430+7748C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146835 | |||||||
| chr13:28147054 | G | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+7967G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147054 | |||||||
| chr13:28147078 | C | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+7991C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147078 | |||||||
| chr13:28147274 | A | G | 249 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.430+8187A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147274 | |||||||
| chr13:28147334 | G | GT | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+8252dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28147334 | ||||||
| chr13:28147370 | A | C | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430+8283A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147370 | |||||||
| chr13:28147424 | C | CTT | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+8338_430+8339d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28147424 | ||||||
| chr13:28147767 | A | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430+8680A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147767 | |||||||
| chr13:28147888 | ATTCT | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+8802_430+8805d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147888 | |||||||
| chr13:28148046 | G | T | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+8959G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148046 | |||||||
| chr13:28148112 | T | C | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+9025T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148112 | |||||||
| chr13:28148306 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.430+9219G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148306 | |||||||
| chr13:28148588 | C | G | 8 | a0001c0001t0001g0056 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
8 | HG02071.hp2 HG02083.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+9501C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148588 | |||||||
| chr13:28148683 | C | A | 1 | a0001c0001t0048g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430+9596C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148683 | |||||||
| chr13:28148857 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+9770A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148857 | |||||||
| chr13:28148903 | T | A | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+9816T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148903 | |||||||
| chr13:28148923 | C | T | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+9836C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148923 | |||||||
| chr13:28149018 | C | T | 2 | a0001c0001t0026g0239 a0001c0007t0021g0151 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+9931C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149018 | |||||||
| chr13:28149038 | C | G | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+9951C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149038 | |||||||
| chr13:28149058 | T | TA | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+9980dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28149058 | ||||||
| chr13:28149192 | T | C | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+10105T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149192 | |||||||
| chr13:28149311 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.430+10224C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149311 | |||||||
| chr13:28149371 | C | T | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+10284C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149371 | |||||||
| chr13:28149377 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0050g0050 a0001c0001t0051g0099 |
3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.430+10290A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149377 | |||||||
| chr13:28149608 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.430+10521T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149608 | |||||||
| chr13:28149648 | GT | G | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+10562delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149648 | |||||||
| chr13:28149798 | G | A | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+10711G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149798 | |||||||
| chr13:28149809 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+10722G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149809 | |||||||
| chr13:28149811 | C | A | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+10724C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149811 | |||||||
| chr13:28149817 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430+10730G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149817 | |||||||
| chr13:28150174 | A | G | 35 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(32): Show |
35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.430+11087A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150174 | |||||||
| chr13:28150367 | T | C | 1 | a0001c0001t0006g0132 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.430+11280T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150367 | |||||||
| chr13:28150391 | C | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+11304C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150391 | |||||||
| chr13:28150466 | A | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+11379A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150466 | |||||||
| chr13:28150499 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
3 | HG02886.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.430+11412C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150499 | |||||||
| chr13:28150612 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430+11525A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150612 | |||||||
| chr13:28150621 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.430+11534A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150621 | |||||||
| chr13:28150637 | C | CA | 13 | a0001c0001t0001g0033 a0001c0001t0001g0156 a0001c0001t0002g0201 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+11567dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28150637 | ||||||
| chr13:28150637 | CA | C | 43 | a0001c0001t0002g0002 a0001c0001t0002g0143 a0001c0001t0002g0164 others(40): Show |
43 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.430+11567delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28150637 | ||||||
| chr13:28150709 | T | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.430+11622T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150709 | |||||||
| chr13:28151021 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430+11934A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151021 | |||||||
| chr13:28151041 | C | T | 1 | a0001c0001t0004g0055 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.430+11954C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151041 | |||||||
| chr13:28151325 | C | G | 3 | a0001c0001t0011g0184 a0001c0001t0019g0185 a0001c0001t0042g0186 |
3 | HG02109.hp1 HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.430+12238C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151325 | |||||||
| chr13:28151375 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.430+12288C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151375 | |||||||
| chr13:28151489 | T | A | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+12402T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151489 | |||||||
| chr13:28151514 | CA | C | 23 | a0001c0001t0002g0164 a0001c0001t0004g0043 a0001c0001t0005g0117 others(20): Show |
23 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.430+12439delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28151514 | ||||||
| chr13:28151800 | T | C | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.430+12713T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151800 | |||||||
| chr13:28151956 | C | G | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+12869C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151956 | |||||||
| chr13:28152045 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+12958A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152045 | |||||||
| chr13:28152053 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+12966A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152053 | |||||||
| chr13:28152127 | A | G | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+13040A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152127 | |||||||
| chr13:28152449 | T | C | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+13362T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152449 | |||||||
| chr13:28152582 | G | GA | 7 | a0001c0001t0001g0103 a0001c0001t0002g0201 a0001c0001t0004g0052 others(4): Show |
7 | HG02135.hp1 HG02602.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+13504dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28152582 | ||||||
| chr13:28152630 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+13543A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152630 | |||||||
| chr13:28152692 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+13605G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152692 | |||||||
| chr13:28152694 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+13607T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152694 | |||||||
| chr13:28152919 | G | C | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+13832G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152919 | |||||||
| chr13:28153232 | C | CT | 52 | a0001c0001t0001g0054 a0001c0001t0001g0089 a0001c0001t0001g0095 others(49): Show |
52 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.430+14167dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28153232 | ||||||
| chr13:28153232 | C | CTT | 53 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(50): Show |
53 | HG00438.hp2 HG00597.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.430+14166_430+1416 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28153232 | ||||||
| chr13:28153232 | C | CTTT | 20 | a0001c0001t0002g0036 a0001c0001t0002g0144 a0001c0001t0002g0149 others(17): Show |
20 | HG00597.hp1 HG00639.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.430+14165_430+1416 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28153232 | ||||||
| chr13:28153292 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+14205A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153292 | |||||||
| chr13:28153391 | A | G | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+14304A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153391 | |||||||
| chr13:28153522 | C | A | 2 | a0001c0001t0026g0239 a0001c0007t0021g0151 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+14435C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153522 | |||||||
| chr13:28153559 | G | C | 1 | a0001c0004t0004g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.430+14472G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153559 | |||||||
| chr13:28153598 | T | C | 1 | a0001c0001t0007g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.430+14511T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153598 | |||||||
| chr13:28153651 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+14564A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153651 | |||||||
| chr13:28153705 | A | G | 3 | a0001c0001t0008g0245 a0001c0001t0008g0246 a0001c0001t0008g0247 |
3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430+14618A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153705 | |||||||
| chr13:28153731 | C | G | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+14644C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153731 | |||||||
| chr13:28153889 | G | A | 72 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.430+14802G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153889 | |||||||
| chr13:28153912 | T | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0014g0113 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+14825T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153912 | |||||||
| chr13:28153942 | G | C | 1 | a0001c0001t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.430+14855G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153942 | |||||||
| chr13:28153996 | G | C | 4 | a0001c0001t0013g0016 a0001c0001t0013g0127 a0001c0001t0013g0128 others(1): Show |
4 | HG00099.hp2 HG03225.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+14909G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153996 | |||||||
| chr13:28154021 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+14934T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154021 | |||||||
| chr13:28154112 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+15025C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154112 | |||||||
| chr13:28154300 | T | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+15213T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154300 | |||||||
| chr13:28154329 | C | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+15242C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154329 | |||||||
| chr13:28154342 | G | A | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.430+15255G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154342 | |||||||
| chr13:28154449 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+15362C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154449 | |||||||
| chr13:28154536 | C | G | 1 | a0002c0005t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.430+15449C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154536 | |||||||
| chr13:28154564 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.430+15477G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154564 | |||||||
| chr13:28154644 | T | G | 58 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(55): Show |
58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.430+15557T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154644 | |||||||
| chr13:28154785 | C | G | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.430+15698C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154785 | |||||||
| chr13:28154807 | GT | G | 36 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0002g0002 others(33): Show |
36 | HG00099.hp2 HG01496.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.430+15735delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28154807 | ||||||
| chr13:28154807 | GTT | G | 24 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(21): Show |
24 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.430+15734_430+1573 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28154807 | ||||||
| chr13:28154819 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+15732T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154819 | |||||||
| chr13:28154828 | C | CT | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+15751dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28154828 | ||||||
| chr13:28154914 | G | A | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+15827G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154914 | |||||||
| chr13:28154940 | C | T | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+15853C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154940 | |||||||
| chr13:28154946 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430+15859G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154946 | |||||||
| chr13:28155018 | C | T | 4 | a0001c0001t0001g0086 a0001c0001t0015g0250 a0001c0001t0029g0249 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+15931C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155018 | |||||||
| chr13:28155067 | T | C | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+15980T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155067 | |||||||
| chr13:28155111 | C | T | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+16024C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155111 | |||||||
| chr13:28155402 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0050g0050 a0001c0001t0051g0099 |
3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.430+16315C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155402 | |||||||
| chr13:28155450 | T | C | 249 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.430+16363T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155450 | |||||||
| chr13:28155655 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.430+16568G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155655 | |||||||
| chr13:28155658 | T | G | 1 | a0001c0001t0041g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.430+16571T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155658 | |||||||
| chr13:28155683 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+16596T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155683 | |||||||
| chr13:28155689 | C | T | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+16602C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155689 | |||||||
| chr13:28155709 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+16622T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155709 | |||||||
| chr13:28155725 | A | G | 7 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0146 others(4): Show |
7 | HG00438.hp2 NA18941.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+16638A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155725 | |||||||
| chr13:28155729 | A | T | 1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+16642A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155729 | |||||||
| chr13:28155734 | T | C | 1 | a0001c0001t0014g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430+16647T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155734 | |||||||
| chr13:28155816 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+16729C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155816 | |||||||
| chr13:28155886 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+16799T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155886 | |||||||
| chr13:28155886 | T | G | 74 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.430+16799T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155886 | |||||||
| chr13:28155966 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+16879C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155966 | |||||||
| chr13:28155984 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+16897A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155984 | |||||||
| chr13:28156155 | G | T | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.430+17068G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156155 | |||||||
| chr13:28156185 | AAAG | A | 17 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
17 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.430+17103_430+1710 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156185 | ||||||
| chr13:28156216 | G | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+17129G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156216 | |||||||
| chr13:28156548 | T | C | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+17461T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156548 | |||||||
| chr13:28156558 | C | G | 3 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 |
3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.430+17471C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156558 | |||||||
| chr13:28156831 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-17441A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156831 | |||||||
| chr13:28156869 | C | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-17403C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156869 | |||||||
| chr13:28156901 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-17371G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156901 | |||||||
| chr13:28156992 | C | CA | 72 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0044 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.431-17253dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | ||||||
| chr13:28156992 | C | CAA | 36 | a0001c0001t0001g0029 a0001c0001t0001g0213 a0001c0001t0002g0037 others(33): Show |
36 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.431-17254_431-1725 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | ||||||
| chr13:28156992 | CA | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0085 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-17253delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | ||||||
| chr13:28156992 | CAAAAAAA others(2): Show |
C | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-17261_431-1725 others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | ||||||
| chr13:28157047 | T | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-17225T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157047 | |||||||
| chr13:28157411 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.431-16861G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157411 | |||||||
| chr13:28157436 | A | G | 1 | a0001c0001t0005g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.431-16836A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157436 | |||||||
| chr13:28157514 | C | T | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-16758C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157514 | |||||||
| chr13:28157615 | G | A | 3 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 |
3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.431-16657G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157615 | |||||||
| chr13:28158041 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0014g0113 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-16231C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158041 | |||||||
| chr13:28158075 | T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-16197T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158075 | |||||||
| chr13:28158164 | G | A | 72 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.431-16108G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158164 | |||||||
| chr13:28158181 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-16091A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158181 | |||||||
| chr13:28158200 | A | G | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-16072A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158200 | |||||||
| chr13:28158221 | T | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-16051T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158221 | |||||||
| chr13:28158251 | A | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-16021A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158251 | |||||||
| chr13:28158301 | G | T | 131 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(128): Show |
131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.431-15971G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158301 | |||||||
| chr13:28158326 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.431-15946A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158326 | |||||||
| chr13:28158349 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.431-15923G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158349 | |||||||
| chr13:28158594 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-15678T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158594 | |||||||
| chr13:28158620 | G | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-15652G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158620 | |||||||
| chr13:28158672 | A | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.431-15600A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158672 | |||||||
| chr13:28158706 | G | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-15566G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158706 | |||||||
| chr13:28158775 | G | T | 1 | a0001c0001t0006g0015 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.431-15497G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158775 | |||||||
| chr13:28158803 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.431-15469G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158803 | |||||||
| chr13:28158835 | G | A | 22 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(19): Show |
22 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.431-15437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158835 | |||||||
| chr13:28158901 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.431-15371G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158901 | |||||||
| chr13:28158995 | G | A | 69 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(66): Show |
69 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.431-15277G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158995 | |||||||
| chr13:28159107 | G | A | 131 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(128): Show |
131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.431-15165G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159107 | |||||||
| chr13:28159136 | T | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-15136T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159136 | |||||||
| chr13:28159138 | A | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-15134A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159138 | |||||||
| chr13:28159224 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-15048A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159224 | |||||||
| chr13:28159404 | G | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-14868G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159404 | |||||||
| chr13:28159405 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-14867T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159405 | |||||||
| chr13:28159477 | C | T | 2 | a0001c0001t0026g0239 a0001c0007t0021g0151 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.431-14795C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159477 | |||||||
| chr13:28159504 | A | G | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.431-14768A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159504 | |||||||
| chr13:28159636 | T | C | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.431-14636T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159636 | |||||||
| chr13:28159924 | G | GT | 12 | a0001c0001t0001g0092 a0001c0001t0002g0011 a0001c0001t0002g0012 others(9): Show |
12 | HG02083.hp1 HG02132.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.431-14336dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28159924 | ||||||
| chr13:28159924 | G | T | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-14348G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159924 | |||||||
| chr13:28160237 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0049g0154 |
2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.431-14035C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160237 | |||||||
| chr13:28160247 | C | A | 2 | a0001c0001t0004g0068 a0001c0008t0001g0069 |
2 | HG01358.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.431-14025C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160247 | |||||||
| chr13:28160328 | T | C | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.431-13944T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160328 | |||||||
| chr13:28160395 | T | A | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-13877T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160395 | |||||||
| chr13:28160518 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-13754G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160518 | |||||||
| chr13:28160636 | A | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-13636A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160636 | |||||||
| chr13:28160637 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-13635T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160637 | |||||||
| chr13:28160642 | C | G | 73 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(70): Show |
73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.431-13630C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160642 | |||||||
| chr13:28160752 | G | C | 3 | a0001c0001t0002g0191 a0001c0001t0002g0235 a0001c0001t0003g0236 |
3 | NA19062.hp2 NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.431-13520G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160752 | |||||||
| chr13:28160795 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.431-13477T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160795 | |||||||
| chr13:28160845 | G | A | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-13427G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160845 | |||||||
| chr13:28160847 | T | A | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.431-13425T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160847 | |||||||
| chr13:28160936 | G | T | 1 | a0001c0001t0016g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.431-13336G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160936 | |||||||
| chr13:28161662 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0004g0087 a0001c0001t0004g0088 |
3 | HG01346.hp1 HG01433.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.431-12610T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161662 | |||||||
| chr13:28161847 | A | G | 1 | a0001c0002t0012g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.431-12425A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161847 | |||||||
| chr13:28161921 | G | A | 1 | a0001c0001t0006g0132 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.431-12351G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161921 | |||||||
| chr13:28161924 | A | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.431-12348A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161924 | |||||||
| chr13:28162022 | A | G | 3 | a0001c0001t0008g0245 a0001c0001t0008g0246 a0001c0001t0008g0247 |
3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.431-12250A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162022 | |||||||
| chr13:28162030 | T | C | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.431-12242T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162030 | |||||||
| chr13:28162098 | A | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0003g0008 others(1): Show |
4 | HG02083.hp1 NA18979.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-12174A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162098 | |||||||
| chr13:28162307 | G | A | 56 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(53): Show |
56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.431-11965G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162307 | |||||||
| chr13:28162333 | C | T | 1 | a0001c0001t0010g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.431-11939C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162333 | |||||||
| chr13:28162410 | T | C | 58 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(55): Show |
58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.431-11862T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162410 | |||||||
| chr13:28162489 | A | C | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-11783A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162489 | |||||||
| chr13:28162555 | G | A | 1 | a0001c0003t0014g0084 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-11717G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162555 | |||||||
| chr13:28162624 | G | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-11648G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162624 | |||||||
| chr13:28162644 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0216 |
2 | NA19002.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.431-11628C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162644 | |||||||
| chr13:28162646 | T | TAA | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.431-11615_431-1161 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28162646 | ||||||
| chr13:28162732 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.431-11540A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162732 | |||||||
| chr13:28162833 | C | A | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-11439C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162833 | |||||||
| chr13:28162949 | T | C | 7 | a0001c0001t0002g0193 a0001c0001t0002g0234 a0001c0001t0003g0215 others(4): Show |
7 | HG01261.hp2 NA18948.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-11323T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162949 | |||||||
| chr13:28163132 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.431-11140T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163132 | |||||||
| chr13:28163212 | A | C | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.431-11060A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163212 | |||||||
| chr13:28163311 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-10961A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163311 | |||||||
| chr13:28163502 | A | G | 56 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(53): Show |
56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.431-10770A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163502 | |||||||
| chr13:28163652 | T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-10620T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163652 | |||||||
| chr13:28163715 | A | G | 5 | a0001c0001t0001g0134 a0001c0001t0001g0157 a0001c0001t0004g0153 others(2): Show |
5 | HG00438.hp1 NA18941.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-10557A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163715 | |||||||
| chr13:28163717 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-10555A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163717 | |||||||
| chr13:28163812 | G | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-10460G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163812 | |||||||
| chr13:28163824 | A | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-10448A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163824 | |||||||
| chr13:28163861 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431-10411T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163861 | |||||||
| chr13:28164052 | C | T | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.431-10220C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164052 | |||||||
| chr13:28164468 | A | G | 2 | a0001c0001t0026g0239 a0001c0007t0021g0151 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.431-9804A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164468 | |||||||
| chr13:28164507 | T | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-9765T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164507 | |||||||
| chr13:28164528 | T | A | 2 | a0001c0001t0002g0233 a0001c0001t0002g0240 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.431-9744T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164528 | |||||||
| chr13:28164794 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-9478A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164794 | |||||||
| chr13:28164918 | A | AT | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-9345dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28164918 | ||||||
| chr13:28164963 | A | G | 75 | a0001c0001t0001g0111 a0001c0001t0001g0213 a0001c0001t0002g0002 others(72): Show |
75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.431-9309A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164963 | |||||||
| chr13:28165097 | G | A | 5 | a0001c0001t0008g0007 a0001c0001t0008g0245 a0001c0001t0008g0246 others(2): Show |
5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-9175G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165097 | |||||||
| chr13:28165243 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-9029A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165243 | |||||||
| chr13:28165283 | C | CT | 79 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0001g0213 others(76): Show |
79 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.431-8972dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28165283 | ||||||
| chr13:28165283 | C | CTT | 20 | a0001c0001t0003g0224 a0001c0001t0003g0232 a0001c0001t0005g0117 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.431-8973_431-8972d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28165283 | ||||||
| chr13:28165283 | C | CTTT | 7 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(4): Show |
7 | HG00639.hp2 HG01099.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-8974_431-8972d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28165283 | ||||||
| chr13:28165313 | G | A | 1 | a0001c0001t0004g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.431-8959G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165313 | |||||||
| chr13:28165324 | T | C | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-8948T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165324 | |||||||
| chr13:28165753 | C | A | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-8519C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165753 | |||||||
| chr13:28165856 | T | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-8416T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165856 | |||||||
| chr13:28166206 | A | G | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-8066A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166206 | |||||||
| chr13:28166551 | T | C | 11 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(8): Show |
11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-7721T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166551 | |||||||
| chr13:28166609 | A | G | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-7663A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166609 | |||||||
| chr13:28166643 | C | T | 1 | a0001c0001t0004g0153 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.431-7629C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166643 | |||||||
| chr13:28166689 | G | A | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-7583G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166689 | |||||||
| chr13:28166790 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-7482G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166790 | |||||||
| chr13:28166964 | C | T | 1 | a0001c0001t0009g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.431-7308C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166964 | |||||||
| chr13:28167082 | A | AT | 87 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0111 others(84): Show |
87 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.431-7168dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28167082 | ||||||
| chr13:28167082 | A | T | 31 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(28): Show |
31 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.431-7190A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167082 | |||||||
| chr13:28167093 | T | A | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-7179T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167093 | |||||||
| chr13:28167233 | C | G | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.431-7039C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167233 | |||||||
| chr13:28167326 | A | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-6946A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167326 | |||||||
| chr13:28167347 | A | T | 15 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(12): Show |
15 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-6925A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167347 | |||||||
| chr13:28167363 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.431-6909G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167363 | |||||||
| chr13:28167436 | T | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-6836T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167436 | |||||||
| chr13:28167452 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.431-6820C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167452 | |||||||
| chr13:28167456 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-6816C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167456 | |||||||
| chr13:28167621 | G | A | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-6651G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167621 | |||||||
| chr13:28167673 | C | CA | 51 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0044 others(48): Show |
51 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.431-6578dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28167673 | ||||||
| chr13:28167677 | A | C | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.431-6595A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167677 | |||||||
| chr13:28167681 | A | C | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.431-6591A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167681 | |||||||
| chr13:28167808 | C | T | 1 | a0001c0001t0006g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.431-6464C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167808 | |||||||
| chr13:28167908 | C | G | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.431-6364C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167908 | |||||||
| chr13:28167924 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.431-6348A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167924 | |||||||
| chr13:28168056 | C | T | 1 | a0001c0003t0014g0084 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-6216C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168056 | |||||||
| chr13:28168176 | C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-6096C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168176 | |||||||
| chr13:28168335 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.431-5937A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168335 | |||||||
| chr13:28168356 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-5916G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168356 | |||||||
| chr13:28168402 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.431-5870A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168402 | |||||||
| chr13:28168402 | A | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.431-5870A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168402 | |||||||
| chr13:28168438 | C | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.431-5834C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168438 | |||||||
| chr13:28168501 | T | C | 2 | a0001c0001t0006g0017 a0001c0001t0006g0020 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.431-5771T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168501 | |||||||
| chr13:28168637 | T | G | 1 | a0001c0001t0009g0217 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.431-5635T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168637 | |||||||
| chr13:28168643 | C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-5629C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168643 | |||||||
| chr13:28168751 | G | A | 3 | a0001c0003t0001g0138 a0001c0003t0004g0136 a0001c0003t0014g0084 |
3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.431-5521G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168751 | |||||||
| chr13:28168773 | C | T | 22 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(19): Show |
22 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.431-5499C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168773 | |||||||
| chr13:28168863 | A | G | 1 | a0001c0001t0042g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.431-5409A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168863 | |||||||
| chr13:28168942 | C | T | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.431-5330C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168942 | |||||||
| chr13:28168994 | C | T | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.431-5278C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168994 | |||||||
| chr13:28169010 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.431-5262C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169010 | |||||||
| chr13:28169015 | C | CA | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-5244dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169015 | ||||||
| chr13:28169051 | A | G | 7 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0146 others(4): Show |
7 | HG00438.hp2 NA18941.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-5221A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169051 | |||||||
| chr13:28169222 | C | CT | 18 | a0001c0001t0001g0034 a0001c0001t0001g0054 a0001c0001t0001g0061 others(15): Show |
18 | HG00438.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-5026dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | ||||||
| chr13:28169222 | C | CTT | 5 | a0001c0001t0006g0053 a0001c0001t0010g0152 a0001c0001t0025g0203 others(2): Show |
5 | HG01358.hp2 HG02258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-5027_431-5026d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | ||||||
| chr13:28169222 | CT | C | 39 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0060 others(36): Show |
39 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.431-5026delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | ||||||
| chr13:28169222 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0231 a0001c0001t0009g0192 |
3 | HG02647.hp1 NA18943.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.431-5035_431-5026d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | ||||||
| chr13:28169222 | CTTTTTTT others(4): Show |
C | 67 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(64): Show |
67 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.431-5036_431-5026d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | ||||||
| chr13:28169373 | G | C | 1 | a0001c0001t0048g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.431-4899G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169373 | |||||||
| chr13:28169384 | C | G | 1 | a0001c0001t0056g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431-4888C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169384 | |||||||
| chr13:28169398 | G | T | 58 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(55): Show |
58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.431-4874G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169398 | |||||||
| chr13:28169527 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431-4745G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169527 | |||||||
| chr13:28169550 | C | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0032 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-4722C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169550 | |||||||
| chr13:28169658 | C | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-4614C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169658 | |||||||
| chr13:28169724 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.431-4548A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169724 | |||||||
| chr13:28169770 | C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.431-4502C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169770 | |||||||
| chr13:28169786 | C | T | 1 | a0001c0001t0007g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.431-4486C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169786 | |||||||
| chr13:28170228 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.431-4044A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170228 | |||||||
| chr13:28170280 | A | G | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-3992A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170280 | |||||||
| chr13:28170347 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-3925A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170347 | |||||||
| chr13:28170451 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-3821T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170451 | |||||||
| chr13:28170472 | T | A | 36 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(33): Show |
36 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.431-3800T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170472 | |||||||
| chr13:28170767 | CATAAG | C | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-3500_431-3496d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28170767 | ||||||
| chr13:28171043 | G | A | 6 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-3229G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171043 | |||||||
| chr13:28171275 | T | C | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.431-2997T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171275 | |||||||
| chr13:28171275 | T | TTCTC | 134 | a0001c0001t0001g0101 a0001c0001t0001g0156 a0001c0001t0001g0213 others(131): Show |
134 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.431-2994_431-2993i others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28171275 | ||||||
| chr13:28171476 | G | A | 1 | a0001c0001t0007g0237 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.431-2796G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171476 | |||||||
| chr13:28171535 | G | A | 1 | a0001c0001t0006g0015 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.431-2737G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171535 | |||||||
| chr13:28171645 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-2627A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171645 | |||||||
| chr13:28171684 | C | A | 1 | a0001c0001t0013g0016 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.431-2588C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171684 | |||||||
| chr13:28172019 | T | C | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-2253T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172019 | |||||||
| chr13:28172046 | A | G | 1 | a0001c0001t0011g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431-2226A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172046 | |||||||
| chr13:28172289 | T | A | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1983T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172289 | |||||||
| chr13:28172480 | T | G | 1 | a0001c0001t0024g0228 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-1792T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172480 | |||||||
| chr13:28172492 | A | G | 1 | a0001c0001t0024g0228 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-1780A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172492 | |||||||
| chr13:28172648 | C | T | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-1624C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172648 | |||||||
| chr13:28172649 | T | C | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.431-1623T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172649 | |||||||
| chr13:28172774 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.431-1498A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172774 | |||||||
| chr13:28172873 | A | G | 1 | a0001c0001t0006g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.431-1399A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172873 | |||||||
| chr13:28172955 | C | A | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1317C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172955 | |||||||
| chr13:28172985 | C | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.431-1287C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172985 | |||||||
| chr13:28173232 | C | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-1040C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173232 | |||||||
| chr13:28173533 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-739A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173533 | |||||||
| chr13:28173682 | A | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-590A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173682 | |||||||
| chr13:28173752 | A | G | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.431-520A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173752 | |||||||
| chr13:28173920 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-352C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173920 | |||||||
| chr13:28173963 | T | G | 1 | a0001c0001t0053g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.431-309T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173963 | |||||||
| chr13:28174070 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-202G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28174070 | |||||||
| chr13:28174132 | A | G | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.431-140A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28174132 | |||||||
| chr13:28174918 | G | C | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.552+525G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28174918 | |||||||
| chr13:28174944 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.552+551T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28174944 | |||||||
| chr13:28175161 | A | G | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.552+768A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175161 | |||||||
| chr13:28175178 | A | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.552+785A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175178 | |||||||
| chr13:28175207 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.552+814G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175207 | |||||||
| chr13:28175351 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.552+958A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175351 | |||||||
| chr13:28175393 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.552+1000G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175393 | |||||||
| chr13:28175594 | T | C | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.553-899T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175594 | |||||||
| chr13:28175657 | G | A | 2 | a0001c0001t0003g0215 a0001c0001t0003g0221 |
2 | NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.553-836G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175657 | |||||||
| chr13:28175877 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.553-616C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175877 | |||||||
| chr13:28175911 | G | T | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.553-582G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175911 | |||||||
| chr13:28175992 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.553-501C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175992 | |||||||
| chr13:28176048 | G | A | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.553-445G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28176048 | |||||||
| chr13:28176406 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.553-87G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28176406 | |||||||
| chr13:28176800 | A | C | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.619+241A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28176800 | |||||||
| chr13:28176847 | T | TA | 7 | a0001c0001t0004g0066 a0001c0001t0017g0204 a0001c0001t0017g0205 others(4): Show |
7 | HG01261.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.619+299dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 28176847 | ||||||
| chr13:28176854 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.619+295A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28176854 | |||||||
| chr13:28177013 | A | C | 1 | a0001c0001t0004g0104 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.619+454A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177013 | |||||||
| chr13:28177226 | AT | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.620-636delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 28177226 | ||||||
| chr13:28177249 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.620-616T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177249 | |||||||
| chr13:28177468 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.620-397A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177468 | |||||||
| chr13:28177542 | T | C | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-323T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177542 | |||||||
| chr13:28177705 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.620-160T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177705 | |||||||
| chr13:28177770 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-95A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177770 | |||||||
| chr13:28177800 | A | G | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.620-65A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177800 | |||||||
| chr13:28177817 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.620-48G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177817 | |||||||
| chr13:28177827 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.620-38A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177827 | |||||||
| chr13:28177978 | A | C | 70 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(67): Show |
70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.690+43A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28177978 | |||||||
| chr13:28178238 | T | C | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.690+303T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178238 | |||||||
| chr13:28178240 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.690+305T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178240 | |||||||
| chr13:28178257 | G | A | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.690+322G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178257 | |||||||
| chr13:28178903 | T | C | 1 | a0001c0001t0003g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.690+968T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178903 | |||||||
| chr13:28178999 | AC | A | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.690+1065delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178999 | |||||||
| chr13:28179006 | T | C | 2 | a0001c0001t0002g0225 a0001c0001t0022g0226 |
2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.690+1071T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179006 | |||||||
| chr13:28179286 | T | C | 1 | a0001c0001t0007g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.690+1351T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179286 | |||||||
| chr13:28179472 | T | C | 1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.690+1537T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179472 | |||||||
| chr13:28179485 | C | T | 1 | a0001c0001t0008g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.690+1550C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179485 | |||||||
| chr13:28179508 | A | G | 73 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(70): Show |
73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.690+1573A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179508 | |||||||
| chr13:28179528 | A | G | 1 | a0001c0001t0004g0088 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.690+1593A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179528 | |||||||
| chr13:28179594 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+1659C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179594 | |||||||
| chr13:28179602 | G | A | 8 | a0001c0001t0002g0193 a0001c0001t0002g0219 a0001c0001t0002g0234 others(5): Show |
8 | HG00597.hp1 HG01261.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+1667G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179602 | |||||||
| chr13:28179633 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.690+1698G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179633 | |||||||
| chr13:28179670 | C | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+1735C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179670 | |||||||
| chr13:28179707 | C | CA | 43 | a0001c0001t0001g0026 a0001c0001t0002g0149 a0001c0001t0004g0052 others(40): Show |
43 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.690+1787dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28179707 | ||||||
| chr13:28179751 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+1816C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179751 | |||||||
| chr13:28179948 | A | G | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.690+2013A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179948 | |||||||
| chr13:28180461 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+2526G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28180461 | |||||||
| chr13:28180743 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+2808T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28180743 | |||||||
| chr13:28180821 | A | G | 4 | a0001c0001t0011g0187 a0001c0001t0011g0242 a0001c0001t0019g0238 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+2886A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28180821 | |||||||
| chr13:28181038 | A | T | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.690+3103A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181038 | |||||||
| chr13:28181067 | A | C | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+3132A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181067 | |||||||
| chr13:28181236 | C | G | 61 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0026 others(58): Show |
61 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.690+3301C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181236 | |||||||
| chr13:28181400 | C | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+3465C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181400 | |||||||
| chr13:28181460 | C | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+3525C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181460 | |||||||
| chr13:28181504 | C | CA | 31 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0032 others(28): Show |
31 | HG00438.hp2 HG01099.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.690+3593dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28181504 | ||||||
| chr13:28181504 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0105 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.690+3584_690+3593d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28181504 | ||||||
| chr13:28181721 | A | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+3786A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181721 | |||||||
| chr13:28182311 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+4376A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182311 | |||||||
| chr13:28182418 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.690+4483G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182418 | |||||||
| chr13:28182920 | C | T | 4 | a0001c0001t0025g0203 a0001c0001t0026g0239 a0001c0001t0038g0243 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+4985C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182920 | |||||||
| chr13:28182921 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.690+4986A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182921 | |||||||
| chr13:28182940 | C | T | 132 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(129): Show |
132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.690+5005C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182940 | |||||||
| chr13:28183727 | A | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+5792A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28183727 | |||||||
| chr13:28183900 | G | A | 131 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(128): Show |
131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.690+5965G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28183900 | |||||||
| chr13:28183976 | ACT | A | 5 | a0001c0001t0008g0007 a0001c0001t0008g0245 a0001c0001t0008g0246 others(2): Show |
5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+6044_690+6045d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28183976 | ||||||
| chr13:28184013 | A | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+6078A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184013 | |||||||
| chr13:28184015 | G | A | 17 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(14): Show |
17 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.690+6080G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184015 | |||||||
| chr13:28184267 | ATAAT | A | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.690+6335_690+6338d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28184267 | ||||||
| chr13:28184339 | GA | G | 12 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.690+6405delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184339 | |||||||
| chr13:28184456 | G | A | 14 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.690+6521G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184456 | |||||||
| chr13:28184466 | C | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+6531C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184466 | |||||||
| chr13:28184501 | G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+6566G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184501 | |||||||
| chr13:28184828 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.690+6893A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184828 | |||||||
| chr13:28184833 | T | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.690+6898T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184833 | |||||||
| chr13:28184900 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.690+6965C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184900 | |||||||
| chr13:28185055 | G | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+7120G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185055 | |||||||
| chr13:28185095 | T | G | 2 | a0001c0001t0006g0014 a0001c0001t0045g0051 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.690+7160T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185095 | |||||||
| chr13:28185100 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+7165A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185100 | |||||||
| chr13:28185151 | C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.690+7216C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185151 | |||||||
| chr13:28185167 | A | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+7232A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185167 | |||||||
| chr13:28185361 | G | A | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.690+7426G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185361 | |||||||
| chr13:28185493 | C | T | 1 | a0001c0001t0009g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.690+7558C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185493 | |||||||
| chr13:28185715 | G | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+7780G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185715 | |||||||
| chr13:28185747 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.690+7812A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185747 | |||||||
| chr13:28185765 | C | T | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.690+7830C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185765 | |||||||
| chr13:28185846 | G | A | 2 | a0001c0001t0016g0040 a0001c0001t0036g0041 |
2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.690+7911G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185846 | |||||||
| chr13:28186176 | A | AATACAAA others(324): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.690+8258_690+8259i others(333): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28186176 | ||||||
| chr13:28186548 | AGTTT | A | 88 | a0001c0001t0001g0094 a0001c0001t0001g0129 a0001c0001t0001g0130 others(85): Show |
88 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.690+8618_690+8621d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28186548 | ||||||
| chr13:28186719 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+8784A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186719 | |||||||
| chr13:28186803 | A | G | 144 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(141): Show |
144 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.690+8868A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186803 | |||||||
| chr13:28186903 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.690+8968A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186903 | |||||||
| chr13:28186911 | C | G | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+8976C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186911 | |||||||
| chr13:28187270 | C | T | 1 | a0001c0001t0005g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.690+9335C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187270 | |||||||
| chr13:28187357 | A | G | 1 | a0001c0001t0045g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.690+9422A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187357 | |||||||
| chr13:28187506 | C | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+9571C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187506 | |||||||
| chr13:28187655 | C | T | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.691-9530C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187655 | |||||||
| chr13:28187683 | A | G | 10 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0201 others(7): Show |
10 | HG02080.hp1 HG02135.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-9502A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187683 | |||||||
| chr13:28187726 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0106 others(1): Show |
4 | HG02523.hp2 NA18747.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-9459C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187726 | |||||||
| chr13:28188027 | CTA | C | 3 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0032g0227 |
3 | HG02258.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.691-9156_691-9155d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28188027 | ||||||
| chr13:28188035 | T | G | 9 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.691-9150T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188035 | |||||||
| chr13:28188114 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.691-9071C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188114 | |||||||
| chr13:28188196 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.691-8989T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188196 | |||||||
| chr13:28188221 | A | G | 1 | a0001c0001t0007g0177 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.691-8964A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188221 | |||||||
| chr13:28188250 | A | AT | 145 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(142): Show |
145 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.691-8927dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28188250 | ||||||
| chr13:28188285 | T | A | 1 | a0001c0001t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.691-8900T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188285 | |||||||
| chr13:28188286 | T | G | 1 | a0001c0001t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.691-8899T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188286 | |||||||
| chr13:28188468 | G | C | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.691-8717G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188468 | |||||||
| chr13:28188602 | AAAAG | A | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-8579_691-8576d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28188602 | ||||||
| chr13:28188844 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0085 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.691-8341A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188844 | |||||||
| chr13:28188908 | T | G | 2 | a0001c0001t0001g0155 a0001c0001t0049g0154 |
2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.691-8277T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188908 | |||||||
| chr13:28189159 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.691-8026A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189159 | |||||||
| chr13:28189374 | G | C | 3 | a0001c0001t0001g0058 a0001c0001t0050g0050 a0001c0001t0051g0099 |
3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.691-7811G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189374 | |||||||
| chr13:28189464 | C | T | 3 | a0001c0001t0005g0117 a0001c0001t0005g0183 a0001c0001t0031g0223 |
3 | HG02056.hp2 HG03098.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.691-7721C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189464 | |||||||
| chr13:28189509 | C | G | 3 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 |
3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.691-7676C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189509 | |||||||
| chr13:28189533 | A | G | 1 | a0001c0001t0029g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.691-7652A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189533 | |||||||
| chr13:28189534 | C | CA | 13 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(10): Show |
13 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.691-7647dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28189534 | ||||||
| chr13:28189537 | A | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.691-7648A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189537 | |||||||
| chr13:28189538 | AC | A | 86 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(83): Show |
86 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.691-7646delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189538 | |||||||
| chr13:28189539 | C | A | 63 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.691-7646C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189539 | |||||||
| chr13:28189598 | C | A | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.691-7587C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189598 | |||||||
| chr13:28189732 | A | G | 1 | a0001c0001t0009g0217 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.691-7453A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189732 | |||||||
| chr13:28189900 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0004g0082 |
2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.691-7285T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189900 | |||||||
| chr13:28190033 | C | T | 144 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(141): Show |
144 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.691-7152C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190033 | |||||||
| chr13:28190089 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.691-7096G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190089 | |||||||
| chr13:28190188 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.691-6997G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190188 | |||||||
| chr13:28190460 | TG | T | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-6724delG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190460 | |||||||
| chr13:28190629 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-6556C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190629 | |||||||
| chr13:28190793 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.691-6392T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190793 | |||||||
| chr13:28190864 | C | G | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.691-6321C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190864 | |||||||
| chr13:28190886 | G | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-6299G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190886 | |||||||
| chr13:28191062 | A | T | 1 | a0001c0001t0019g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.691-6123A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191062 | |||||||
| chr13:28191181 | T | C | 57 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(54): Show |
57 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.691-6004T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191181 | |||||||
| chr13:28191272 | C | T | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.691-5913C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191272 | |||||||
| chr13:28191391 | G | T | 2 | a0001c0001t0002g0225 a0001c0001t0022g0226 |
2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.691-5794G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191391 | |||||||
| chr13:28191477 | G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.691-5708G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191477 | |||||||
| chr13:28191537 | C | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-5648C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191537 | |||||||
| chr13:28191803 | T | G | 1 | a0001c0001t0002g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.691-5382T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191803 | |||||||
| chr13:28191818 | C | T | 2 | a0001c0003t0001g0138 a0001c0003t0004g0136 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.691-5367C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191818 | |||||||
| chr13:28191991 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.691-5194C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191991 | |||||||
| chr13:28192016 | C | T | 3 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0148 |
3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.691-5169C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192016 | |||||||
| chr13:28192048 | C | CT | 9 | a0001c0001t0001g0077 a0001c0001t0001g0083 a0001c0001t0001g0135 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-5118dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28192048 | ||||||
| chr13:28192048 | CT | C | 115 | a0001c0001t0001g0061 a0001c0001t0001g0108 a0001c0001t0001g0129 others(112): Show |
115 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.691-5118delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28192048 | ||||||
| chr13:28192048 | CTT | C | 11 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0146 others(8): Show |
11 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-5119_691-5118d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28192048 | ||||||
| chr13:28192127 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-5058C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192127 | |||||||
| chr13:28192357 | C | T | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-4828C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192357 | |||||||
| chr13:28192607 | C | G | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-4578C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192607 | |||||||
| chr13:28192930 | T | C | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.691-4255T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192930 | |||||||
| chr13:28193205 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-3980A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193205 | |||||||
| chr13:28193254 | A | T | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.691-3931A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193254 | |||||||
| chr13:28193284 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.691-3901A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193284 | |||||||
| chr13:28193496 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0033 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-3689C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193496 | |||||||
| chr13:28193604 | G | C | 88 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(85): Show |
88 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.691-3581G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193604 | |||||||
| chr13:28193614 | A | C | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.691-3571A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193614 | |||||||
| chr13:28193705 | T | A | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.691-3480T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193705 | |||||||
| chr13:28193736 | T | TA | 179 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(176): Show |
179 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.691-3429dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193736 | ||||||
| chr13:28193736 | T | TAA | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0081 others(31): Show |
34 | HG01175.hp2 HG01261.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.691-3430_691-3429d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193736 | ||||||
| chr13:28193756 | A | AAC | 12 | a0001c0001t0005g0179 a0001c0001t0005g0188 a0001c0001t0011g0184 others(9): Show |
12 | HG00639.hp2 HG01109.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-3429_691-3428i others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193756 | |||||||
| chr13:28193756 | A | AC | 20 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-3426dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193756 | ||||||
| chr13:28193791 | CT | C | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-3386delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193791 | ||||||
| chr13:28193807 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.691-3378G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193807 | |||||||
| chr13:28193819 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.691-3366A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193819 | |||||||
| chr13:28193847 | G | T | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-3338G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193847 | |||||||
| chr13:28193865 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.691-3320G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193865 | |||||||
| chr13:28193866 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.691-3319T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193866 | |||||||
| chr13:28193885 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.691-3300G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193885 | |||||||
| chr13:28193913 | T | C | 1 | a0001c0001t0003g0010 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-3272T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193913 | |||||||
| chr13:28193914 | T | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.691-3271T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193914 | |||||||
| chr13:28193917 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-3268G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193917 | |||||||
| chr13:28194154 | AAAAT | A | 33 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0036 others(30): Show |
33 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.691-3027_691-3024d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194154 | ||||||
| chr13:28194259 | A | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2926A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194259 | |||||||
| chr13:28194277 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-2908G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194277 | |||||||
| chr13:28194408 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2777A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194408 | |||||||
| chr13:28194437 | CATATATA others(11): Show |
C | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.691-2739_691-2722d others(20): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194437 | ||||||
| chr13:28194450 | G | GTA | 14 | a0001c0001t0002g0225 a0001c0001t0005g0117 a0001c0001t0005g0176 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-2719_691-2718d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194450 | ||||||
| chr13:28194450 | G | GTATA | 6 | a0001c0001t0002g0036 a0001c0001t0002g0167 a0001c0001t0002g0169 others(3): Show |
6 | HG02132.hp2 HG02165.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-2721_691-2718d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194450 | ||||||
| chr13:28194452 | A | G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0166 a0001c0001t0025g0203 |
3 | HG01358.hp2 HG02155.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.691-2733A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194452 | |||||||
| chr13:28194464 | A | AT | 7 | a0001c0001t0002g0002 a0001c0001t0002g0233 a0001c0001t0002g0240 others(4): Show |
7 | HG01167.hp2 HG01891.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2720dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194464 | ||||||
| chr13:28194464 | A | ATT | 4 | a0001c0001t0003g0003 a0001c0001t0008g0007 a0001c0001t0008g0248 others(1): Show |
4 | HG02976.hp2 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-2720_691-2719i others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194464 | ||||||
| chr13:28194464 | A | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.691-2721A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194464 | |||||||
| chr13:28194466 | A | AT | 8 | a0001c0001t0006g0013 a0001c0001t0006g0017 a0001c0001t0006g0019 others(5): Show |
8 | HG01069.hp1 HG01081.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-2700dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | ||||||
| chr13:28194466 | A | ATATATAT others(8): Show |
4 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0126 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | ||||||
| chr13:28194466 | A | ATATATAT others(8): Show |
2 | a0001c0001t0010g0124 a0001c0001t0028g0125 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.691-2718_691-2717i others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | ||||||
| chr13:28194466 | A | ATATATAT others(6): Show |
1 | a0001c0001t0033g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.691-2718_691-2717i others(15): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | ||||||
| chr13:28194466 | A | ATT | 7 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(4): Show |
7 | HG01496.hp1 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2701_691-2700d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | ||||||
| chr13:28194466 | A | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0233 a0001c0001t0002g0240 others(11): Show |
14 | HG01167.hp2 HG01891.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-2719A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194466 | |||||||
| chr13:28194467 | T | TA | 18 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0083 others(15): Show |
18 | HG01071.hp2 HG01099.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194467 | |||||||
| chr13:28194467 | T | TATA | 59 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0038 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194467 | |||||||
| chr13:28194467 | T | TATATA | 11 | a0001c0001t0002g0011 a0001c0001t0002g0037 a0001c0001t0002g0219 others(8): Show |
11 | HG00597.hp1 HG00639.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194467 | |||||||
| chr13:28194468 | T | A | 113 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.691-2717T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194468 | |||||||
| chr13:28194469 | T | A | 73 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0083 others(70): Show |
73 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.691-2716T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194469 | |||||||
| chr13:28194470 | T | A | 87 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.691-2715T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194470 | |||||||
| chr13:28194471 | T | A | 16 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0146 others(13): Show |
16 | HG00639.hp1 HG00639.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.691-2714T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194471 | |||||||
| chr13:28194472 | T | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0004g0066 others(4): Show |
7 | HG00735.hp2 HG01261.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-2713T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194472 | |||||||
| chr13:28194473 | T | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691-2712T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194473 | |||||||
| chr13:28194475 | T | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691-2710T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194475 | |||||||
| chr13:28194546 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.691-2639A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194546 | |||||||
| chr13:28194699 | A | C | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.691-2486A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194699 | |||||||
| chr13:28194722 | C | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.691-2463C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194722 | |||||||
| chr13:28194763 | C | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-2422C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194763 | |||||||
| chr13:28194790 | T | C | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.691-2395T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194790 | |||||||
| chr13:28194879 | C | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691-2306C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194879 | |||||||
| chr13:28194970 | ACTTATT | A | 14 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-2207_691-2202d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194970 | ||||||
| chr13:28195056 | T | G | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-2129T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195056 | |||||||
| chr13:28195114 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.691-2071A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195114 | |||||||
| chr13:28195310 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.691-1875G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195310 | |||||||
| chr13:28195692 | T | A | 1 | a0001c0001t0002g0167 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.691-1493T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195692 | |||||||
| chr13:28196011 | T | C | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.691-1174T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196011 | |||||||
| chr13:28196026 | G | GT | 6 | a0001c0001t0001g0155 a0001c0001t0002g0167 a0001c0001t0008g0244 others(3): Show |
6 | HG01496.hp2 HG02486.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-1146dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28196026 | ||||||
| chr13:28196028 | T | G | 2 | a0001c0001t0016g0040 a0001c0001t0036g0041 |
2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.691-1157T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196028 | |||||||
| chr13:28196279 | A | G | 8 | a0001c0001t0002g0115 a0001c0001t0002g0164 a0001c0001t0002g0168 others(5): Show |
8 | HG02071.hp1 HG02523.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-906A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196279 | |||||||
| chr13:28196306 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.691-879A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196306 | |||||||
| chr13:28196321 | G | A | 144 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(141): Show |
144 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.691-864G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196321 | |||||||
| chr13:28196348 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.691-837A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196348 | |||||||
| chr13:28196353 | G | T | 2 | a0001c0001t0001g0155 a0001c0001t0049g0154 |
2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.691-832G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196353 | |||||||
| chr13:28196468 | T | G | 2 | a0001c0001t0016g0040 a0001c0001t0036g0041 |
2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.691-717T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196468 | |||||||
| chr13:28196531 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.691-654C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196531 | |||||||
| chr13:28197111 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-74A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28197111 | |||||||
| chr13:28197472 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.852+126T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197472 | |||||||
| chr13:28197484 | A | G | 57 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(54): Show |
57 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.852+138A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197484 | |||||||
| chr13:28197512 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.852+166A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197512 | |||||||
| chr13:28197628 | A | G | 5 | a0001c0001t0008g0007 a0001c0001t0008g0245 a0001c0001t0008g0246 others(2): Show |
5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+282A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197628 | |||||||
| chr13:28197674 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.852+328G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197674 | |||||||
| chr13:28197994 | C | T | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+648C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197994 | |||||||
| chr13:28198124 | G | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+778G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198124 | |||||||
| chr13:28198126 | A | G | 2 | a0001c0001t0006g0014 a0001c0001t0045g0051 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.852+780A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198126 | |||||||
| chr13:28198218 | G | A | 2 | a0001c0001t0005g0182 a0001c0001t0007g0180 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.852+872G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198218 | |||||||
| chr13:28198289 | C | CA | 42 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(39): Show |
42 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.852+956dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28198289 | ||||||
| chr13:28198410 | A | G | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+1064A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198410 | |||||||
| chr13:28198655 | T | C | 36 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(33): Show |
36 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.852+1309T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198655 | |||||||
| chr13:28198737 | G | A | 4 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+1391G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198737 | |||||||
| chr13:28199127 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+1781C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199127 | |||||||
| chr13:28199231 | G | T | 56 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(53): Show |
56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.852+1885G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199231 | |||||||
| chr13:28199325 | T | C | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.852+1979T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199325 | |||||||
| chr13:28199333 | T | A | 1 | a0001c0001t0003g0236 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.852+1987T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199333 | |||||||
| chr13:28199467 | T | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+2121T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199467 | |||||||
| chr13:28199498 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.852+2152C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199498 | |||||||
| chr13:28199503 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.852+2157G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199503 | |||||||
| chr13:28199628 | G | A | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+2282G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199628 | |||||||
| chr13:28199720 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+2374A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199720 | |||||||
| chr13:28199727 | C | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+2381C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199727 | |||||||
| chr13:28199853 | C | A | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.852+2507C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199853 | |||||||
| chr13:28200263 | ACT | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+2920_852+2921d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28200263 | ||||||
| chr13:28200360 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+3014T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200360 | |||||||
| chr13:28200421 | G | A | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+3075G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200421 | |||||||
| chr13:28200501 | A | G | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.852+3155A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200501 | |||||||
| chr13:28200525 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+3179C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200525 | |||||||
| chr13:28200607 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.852+3261A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200607 | |||||||
| chr13:28200759 | A | G | 9 | a0001c0001t0002g0115 a0001c0001t0002g0164 a0001c0001t0002g0168 others(6): Show |
9 | HG02071.hp1 HG02155.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.852+3413A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200759 | |||||||
| chr13:28200770 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.852+3424T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200770 | |||||||
| chr13:28200972 | G | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+3626G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200972 | |||||||
| chr13:28201078 | G | A | 3 | a0001c0001t0025g0203 a0001c0001t0038g0243 a0001c0007t0021g0151 |
3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852+3732G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201078 | |||||||
| chr13:28201097 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852+3751A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201097 | |||||||
| chr13:28201159 | C | T | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.852+3813C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201159 | |||||||
| chr13:28201174 | G | A | 33 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(30): Show |
33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.852+3828G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201174 | |||||||
| chr13:28201201 | A | AT | 7 | a0001c0001t0010g0121 a0001c0001t0010g0124 a0001c0001t0010g0126 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+3870dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28201201 | ||||||
| chr13:28201403 | G | A | 2 | a0001c0001t0038g0243 a0001c0007t0021g0151 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852+4057G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201403 | |||||||
| chr13:28201414 | C | T | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.852+4068C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201414 | |||||||
| chr13:28201461 | G | T | 2 | a0001c0003t0001g0138 a0001c0003t0004g0136 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.852+4115G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201461 | |||||||
| chr13:28201487 | A | C | 3 | a0001c0001t0002g0191 a0001c0001t0002g0235 a0001c0001t0003g0236 |
3 | NA19062.hp2 NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.852+4141A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201487 | |||||||
| chr13:28201533 | A | G | 145 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(142): Show |
145 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.852+4187A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201533 | |||||||
| chr13:28201584 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852+4238G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201584 | |||||||
| chr13:28201674 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+4328A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201674 | |||||||
| chr13:28201700 | G | C | 146 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(143): Show |
146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.852+4354G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201700 | |||||||
| chr13:28201727 | G | A | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.852+4381G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201727 | |||||||
| chr13:28201825 | T | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+4479T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201825 | |||||||
| chr13:28201904 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+4558A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201904 | |||||||
| chr13:28201917 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.852+4571C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201917 | |||||||
| chr13:28202052 | AT | A | 14 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(11): Show |
14 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.852+4716delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28202052 | ||||||
| chr13:28202062 | T | C | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+4716T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202062 | |||||||
| chr13:28202320 | T | A | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.852+4974T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202320 | |||||||
| chr13:28202359 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+5013A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202359 | |||||||
| chr13:28202409 | T | C | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+5063T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202409 | |||||||
| chr13:28202494 | G | A | 146 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(143): Show |
146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.852+5148G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202494 | |||||||
| chr13:28202509 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.852+5163T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202509 | |||||||
| chr13:28202568 | T | C | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+5222T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202568 | |||||||
| chr13:28202658 | T | TAC | 16 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0003g0001 others(13): Show |
16 | HG00099.hp1 HG01358.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.852+5332_852+5333d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28202658 | ||||||
| chr13:28202658 | T | TACACACA others(1): Show |
3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+5326_852+5333d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28202658 | ||||||
| chr13:28202683 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.852+5337T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202683 | |||||||
| chr13:28202704 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.852+5358C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202704 | |||||||
| chr13:28202797 | A | G | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.852+5451A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202797 | |||||||
| chr13:28202933 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+5587C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202933 | |||||||
| chr13:28202997 | C | G | 1 | a0001c0001t0007g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.852+5651C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202997 | |||||||
| chr13:28203041 | C | A | 2 | a0001c0001t0001g0075 a0001c0001t0004g0082 |
2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.852+5695C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203041 | |||||||
| chr13:28203365 | A | G | 2 | a0001c0001t0050g0050 a0001c0001t0051g0099 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.852+6019A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203365 | |||||||
| chr13:28203476 | C | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+6130C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203476 | |||||||
| chr13:28203680 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0034 |
2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.852+6334A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203680 | |||||||
| chr13:28203704 | G | A | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.852+6358G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203704 | |||||||
| chr13:28203726 | T | C | 2 | a0001c0001t0031g0223 a0001c0001t0032g0227 |
2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.852+6380T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203726 | |||||||
| chr13:28203756 | C | T | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+6410C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203756 | |||||||
| chr13:28203783 | G | A | 2 | a0001c0001t0002g0225 a0001c0001t0022g0226 |
2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.852+6437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203783 | |||||||
| chr13:28203807 | CT | C | 7 | a0001c0001t0001g0071 a0001c0001t0004g0104 a0001c0001t0017g0204 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+6476delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28203807 | ||||||
| chr13:28203811 | T | C | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+6465T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203811 | |||||||
| chr13:28203812 | T | C | 79 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(76): Show |
79 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.852+6466T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203812 | |||||||
| chr13:28203950 | A | G | 8 | a0001c0001t0001g0109 a0001c0001t0010g0124 a0001c0001t0010g0126 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.852+6604A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203950 | |||||||
| chr13:28203959 | C | T | 6 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0001c0001t0039g0005 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.852+6613C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203959 | |||||||
| chr13:28204519 | A | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+7173A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28204519 | |||||||
| chr13:28204772 | A | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.852+7426A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28204772 | |||||||
| chr13:28205258 | T | G | 94 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(91): Show |
94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.852+7912T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205258 | |||||||
| chr13:28205340 | A | G | 60 | a0001c0001t0001g0095 a0001c0001t0001g0213 a0001c0001t0002g0011 others(57): Show |
60 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.852+7994A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205340 | |||||||
| chr13:28205372 | C | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+8026C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205372 | |||||||
| chr13:28205627 | C | T | 1 | a0001c0001t0014g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.852+8281C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205627 | |||||||
| chr13:28205741 | G | A | 1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.852+8395G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205741 | |||||||
| chr13:28205861 | TA | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG02015.hp1 HG02698.hp2 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.852+8531delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28205861 | ||||||
| chr13:28205873 | A | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+8527A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205873 | |||||||
| chr13:28206029 | C | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.852+8683C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206029 | |||||||
| chr13:28206121 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852+8775A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206121 | |||||||
| chr13:28206207 | A | C | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.852+8861A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206207 | |||||||
| chr13:28206253 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0004g0082 |
2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.852+8907A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206253 | |||||||
| chr13:28206264 | T | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+8918T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206264 | |||||||
| chr13:28206305 | G | A | 1 | a0001c0001t0014g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.852+8959G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206305 | |||||||
| chr13:28206315 | C | CT | 67 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0032 others(64): Show |
67 | HG00597.hp1 HG00735.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.852+8993dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | ||||||
| chr13:28206315 | C | CTT | 5 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 others(2): Show |
5 | HG01891.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+8992_852+8993d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | ||||||
| chr13:28206315 | CT | C | 8 | a0001c0001t0001g0045 a0001c0001t0002g0196 a0001c0001t0002g0216 others(5): Show |
8 | HG01358.hp2 HG02258.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+8993delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | ||||||
| chr13:28206315 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.852+8986_852+8993d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | ||||||
| chr13:28206349 | T | G | 1 | a0001c0001t0005g0183 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.852+9003T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206349 | |||||||
| chr13:28206473 | C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.852+9127C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206473 | |||||||
| chr13:28206738 | G | GT | 51 | a0001c0001t0002g0167 a0001c0001t0002g0201 a0001c0001t0003g0010 others(48): Show |
51 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.852+9404dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206738 | ||||||
| chr13:28207081 | G | T | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+9735G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207081 | |||||||
| chr13:28207113 | T | C | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+9767T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207113 | |||||||
| chr13:28207188 | A | G | 2 | a0001c0001t0003g0142 a0001c0001t0003g0148 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.852+9842A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207188 | |||||||
| chr13:28207362 | C | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+10016C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207362 | |||||||
| chr13:28207418 | C | T | 14 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.852+10072C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207418 | |||||||
| chr13:28207442 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.852+10096A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207442 | |||||||
| chr13:28207625 | GTCTTT | G | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.852+10281_852+1028 others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28207625 | ||||||
| chr13:28207638 | G | C | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+10292G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207638 | |||||||
| chr13:28207659 | T | C | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+10313T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207659 | |||||||
| chr13:28208047 | A | G | 1 | a0001c0001t0007g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.852+10701A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208047 | |||||||
| chr13:28208345 | A | T | 1 | a0001c0001t0010g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.852+10999A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208345 | |||||||
| chr13:28208380 | A | C | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+11034A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208380 | |||||||
| chr13:28208450 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.852+11104A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208450 | |||||||
| chr13:28208465 | G | T | 1 | a0001c0001t0011g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.852+11119G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208465 | |||||||
| chr13:28208467 | T | G | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.852+11121T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208467 | |||||||
| chr13:28208538 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0004g0055 |
2 | HG02165.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.852+11192T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208538 | |||||||
| chr13:28208546 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+11200A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208546 | |||||||
| chr13:28208581 | C | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+11235C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208581 | |||||||
| chr13:28208582 | C | T | 3 | a0001c0001t0025g0203 a0001c0001t0038g0243 a0001c0007t0021g0151 |
3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852+11236C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208582 | |||||||
| chr13:28208589 | G | A | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.852+11243G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208589 | |||||||
| chr13:28208599 | G | A | 6 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0146 others(3): Show |
6 | NA18941.hp2 NA18967.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.852+11253G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208599 | |||||||
| chr13:28208710 | C | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.852+11364C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208710 | |||||||
| chr13:28208884 | T | A | 1 | a0001c0001t0034g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.853-11347T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208884 | |||||||
| chr13:28208922 | T | G | 2 | a0001c0001t0002g0233 a0001c0001t0002g0240 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.853-11309T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208922 | |||||||
| chr13:28209137 | G | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.853-11094G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209137 | |||||||
| chr13:28209531 | T | C | 1 | a0001c0001t0041g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.853-10700T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209531 | |||||||
| chr13:28209566 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-10665A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209566 | |||||||
| chr13:28209603 | A | T | 1 | a0001c0001t0006g0019 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.853-10628A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209603 | |||||||
| chr13:28209751 | TCCTGCCT others(1): Show |
T | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-10464_853-1045 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28209751 | ||||||
| chr13:28209862 | C | T | 1 | a0001c0001t0005g0183 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.853-10369C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209862 | |||||||
| chr13:28209939 | C | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.853-10292C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209939 | |||||||
| chr13:28210078 | G | T | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-10153G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210078 | |||||||
| chr13:28210306 | G | A | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-9925G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210306 | |||||||
| chr13:28210334 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.853-9897G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210334 | |||||||
| chr13:28210774 | C | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-9457C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210774 | |||||||
| chr13:28211012 | C | A | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.853-9219C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211012 | |||||||
| chr13:28211039 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.853-9192G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211039 | |||||||
| chr13:28211068 | A | T | 6 | a0001c0001t0001g0028 a0001c0001t0017g0204 a0001c0001t0017g0205 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-9163A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211068 | |||||||
| chr13:28211069 | T | A | 3 | a0001c0001t0025g0203 a0001c0001t0038g0243 a0001c0007t0021g0151 |
3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.853-9162T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211069 | |||||||
| chr13:28211088 | A | G | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-9143A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211088 | |||||||
| chr13:28211383 | T | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8848T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211383 | |||||||
| chr13:28211546 | T | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-8685T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211546 | |||||||
| chr13:28211657 | C | A | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-8574C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211657 | |||||||
| chr13:28211768 | T | C | 1 | a0001c0001t0002g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.853-8463T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211768 | |||||||
| chr13:28211771 | A | T | 87 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(84): Show |
87 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.853-8460A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211771 | |||||||
| chr13:28211819 | C | T | 60 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0027 others(57): Show |
60 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.853-8412C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211819 | |||||||
| chr13:28212083 | A | G | 72 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.853-8148A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212083 | |||||||
| chr13:28212342 | G | C | 147 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(144): Show |
147 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.853-7889G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212342 | |||||||
| chr13:28212600 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853-7631T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212600 | |||||||
| chr13:28212710 | G | A | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7521G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212710 | |||||||
| chr13:28212740 | A | C | 147 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(144): Show |
147 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.853-7491A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212740 | |||||||
| chr13:28212851 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-7380T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212851 | |||||||
| chr13:28213088 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 others(1): Show |
4 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7143G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213088 | |||||||
| chr13:28213205 | T | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-7026T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213205 | |||||||
| chr13:28213291 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-6940G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213291 | |||||||
| chr13:28213394 | A | G | 1 | a0001c0001t0016g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.853-6837A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213394 | |||||||
| chr13:28213402 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853-6829A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213402 | |||||||
| chr13:28213546 | C | T | 1 | a0001c0001t0005g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-6685C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213546 | |||||||
| chr13:28213639 | G | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-6592G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213639 | |||||||
| chr13:28213702 | C | CA | 22 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0089 others(19): Show |
22 | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-6511dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | ||||||
| chr13:28213702 | C | CAA | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.853-6512_853-6511d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | ||||||
| chr13:28213702 | C | CAAA | 7 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0233 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-6513_853-6511d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | ||||||
| chr13:28213702 | CA | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-6511delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | ||||||
| chr13:28213708 | A | AC | 14 | a0001c0001t0004g0052 a0001c0001t0006g0013 a0001c0001t0006g0014 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-6523_853-6522i others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213708 | |||||||
| chr13:28213709 | A | C | 1 | a0002c0005t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.853-6522A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213709 | |||||||
| chr13:28213906 | A | G | 75 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(72): Show |
75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-6325A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213906 | |||||||
| chr13:28214169 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.853-6062A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214169 | |||||||
| chr13:28214255 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.853-5976A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214255 | |||||||
| chr13:28214396 | GT | G | 14 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(11): Show |
14 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-5834delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214396 | |||||||
| chr13:28214406 | G | A | 146 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(143): Show |
146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.853-5825G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214406 | |||||||
| chr13:28214609 | T | A | 56 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(53): Show |
56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.853-5622T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214609 | |||||||
| chr13:28214619 | A | G | 6 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-5612A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214619 | |||||||
| chr13:28214677 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.853-5554A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214677 | |||||||
| chr13:28215245 | A | G | 1 | a0001c0001t0003g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-4986A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215245 | |||||||
| chr13:28215548 | TGAACCAT others(13): Show |
T | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.853-4681_853-4662d others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28215548 | ||||||
| chr13:28215657 | T | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | HG01099.hp2 HG01167.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.853-4574T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215657 | |||||||
| chr13:28215730 | A | C | 6 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-4501A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215730 | |||||||
| chr13:28215815 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-4416G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215815 | |||||||
| chr13:28215960 | G | C | 88 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(85): Show |
88 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.853-4271G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215960 | |||||||
| chr13:28215982 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.853-4249A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215982 | |||||||
| chr13:28216104 | T | TTTAAG | 148 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(145): Show |
148 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.853-4124_853-4123i others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216104 | ||||||
| chr13:28216198 | A | AG | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-4032dupG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216198 | ||||||
| chr13:28216199 | G | GA | 76 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(73): Show |
76 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.853-4020dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216199 | ||||||
| chr13:28216209 | A | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-4022A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216209 | |||||||
| chr13:28216231 | T | C | 56 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(53): Show |
56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.853-4000T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216231 | |||||||
| chr13:28216280 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853-3951A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216280 | |||||||
| chr13:28216818 | T | TA | 133 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(130): Show |
133 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.853-3401dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216818 | ||||||
| chr13:28216918 | C | A | 1 | a0001c0001t0048g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.853-3313C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216918 | |||||||
| chr13:28216975 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-3256G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216975 | |||||||
| chr13:28217113 | C | CA | 73 | a0001c0001t0001g0026 a0001c0001t0001g0213 a0001c0001t0002g0002 others(70): Show |
73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.853-3104dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217113 | ||||||
| chr13:28217113 | CA | C | 6 | a0001c0001t0005g0179 a0001c0001t0007g0178 a0001c0001t0015g0250 others(3): Show |
6 | HG00735.hp2 HG01433.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-3104delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217113 | ||||||
| chr13:28217113 | CAAAA | C | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-3107_853-3104d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217113 | ||||||
| chr13:28217138 | TACA | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-3086_853-3084d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217138 | ||||||
| chr13:28217290 | T | C | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.853-2941T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217290 | |||||||
| chr13:28217412 | C | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-2819C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217412 | |||||||
| chr13:28217580 | CAAAAAAC others(4): Show |
C | 75 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(72): Show |
75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-2633_853-2623d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217580 | ||||||
| chr13:28217587 | C | CA | 50 | a0001c0001t0001g0089 a0001c0001t0005g0117 a0001c0001t0005g0172 others(47): Show |
50 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.853-2634dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217587 | ||||||
| chr13:28217587 | C | CAA | 6 | a0001c0001t0005g0206 a0001c0001t0008g0007 a0001c0001t0008g0245 others(3): Show |
6 | HG00639.hp1 HG01496.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-2635_853-2634d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217587 | ||||||
| chr13:28217593 | A | G | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-2638A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217593 | |||||||
| chr13:28217598 | C | CA | 17 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(14): Show |
17 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.853-2623dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217598 | ||||||
| chr13:28217669 | A | T | 75 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(72): Show |
75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-2562A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217669 | |||||||
| chr13:28217857 | A | T | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.853-2374A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217857 | |||||||
| chr13:28217961 | C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.853-2270C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217961 | |||||||
| chr13:28218098 | T | C | 2 | a0001c0001t0005g0206 a0001c0001t0030g0161 |
2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.853-2133T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28218098 | |||||||
| chr13:28218106 | T | A | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-2125T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28218106 | |||||||
| chr13:28218426 | AAATC | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-1802_853-1799d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28218426 | ||||||
| chr13:28218588 | A | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.853-1643A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28218588 | |||||||
| chr13:28219149 | A | T | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853-1082A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219149 | |||||||
| chr13:28219422 | C | CT | 75 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(72): Show |
75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-807dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28219422 | ||||||
| chr13:28219521 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.853-710A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219521 | |||||||
| chr13:28219620 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853-611G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219620 | |||||||
| chr13:28219781 | C | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-450C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219781 | |||||||
| chr13:28220011 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.853-220A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28220011 | |||||||
| chr13:28220099 | C | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.853-132C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28220099 | |||||||
| chr13:28220121 | C | T | 17 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(14): Show |
17 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.853-110C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28220121 | |||||||
| chr13:28220597 | A | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+219A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28220597 | |||||||
| chr13:28220824 | T | C | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000+446T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28220824 | |||||||
| chr13:28221016 | G | C | 5 | a0001c0001t0008g0007 a0001c0001t0008g0245 a0001c0001t0008g0246 others(2): Show |
5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+638G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221016 | |||||||
| chr13:28221071 | G | C | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+693G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221071 | |||||||
| chr13:28221121 | A | C | 1 | a0001c0001t0004g0068 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1000+743A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221121 | |||||||
| chr13:28221347 | TA | T | 55 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(52): Show |
55 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1000+980delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28221347 | ||||||
| chr13:28221361 | G | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+983G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221361 | |||||||
| chr13:28221469 | G | T | 146 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(143): Show |
146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1000+1091G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221469 | |||||||
| chr13:28221473 | A | G | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1000+1095A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221473 | |||||||
| chr13:28221639 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1000+1261C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221639 | |||||||
| chr13:28221685 | A | G | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+1307A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221685 | |||||||
| chr13:28221725 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1000+1347T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221725 | |||||||
| chr13:28221912 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+1534C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221912 | |||||||
| chr13:28221956 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000+1578T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221956 | |||||||
| chr13:28222014 | T | A | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1000+1636T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222014 | |||||||
| chr13:28222269 | T | C | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+1891T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222269 | |||||||
| chr13:28222325 | CT | C | 4 | a0001c0001t0013g0016 a0001c0001t0013g0127 a0001c0001t0013g0128 others(1): Show |
4 | HG00099.hp2 HG03225.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+1948delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222325 | |||||||
| chr13:28222335 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1000+1957A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222335 | |||||||
| chr13:28222459 | T | C | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+2081T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222459 | |||||||
| chr13:28222610 | C | G | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1000+2232C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222610 | |||||||
| chr13:28222727 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1000+2349A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222727 | |||||||
| chr13:28222741 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1000+2363C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222741 | |||||||
| chr13:28222784 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1000+2406A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222784 | |||||||
| chr13:28222837 | C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000+2459C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222837 | |||||||
| chr13:28222854 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000+2476C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222854 | |||||||
| chr13:28222936 | G | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+2558G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222936 | |||||||
| chr13:28223287 | A | G | 1 | a0001c0001t0013g0016 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1000+2909A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223287 | |||||||
| chr13:28223294 | T | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000+2916T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223294 | |||||||
| chr13:28223350 | C | CATAG | 5 | a0001c0001t0001g0134 a0001c0001t0001g0157 a0001c0001t0004g0153 others(2): Show |
5 | HG00438.hp1 NA18941.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+2972_1000+297 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223350 | |||||||
| chr13:28223351 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1000+2973C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223351 | |||||||
| chr13:28223378 | A | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+3000A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223378 | |||||||
| chr13:28223549 | GT | G | 28 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(25): Show |
28 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1000+3182delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223549 | ||||||
| chr13:28223586 | G | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1000+3208G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223586 | |||||||
| chr13:28223832 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1000+3454A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223832 | |||||||
| chr13:28223871 | A | AT | 34 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0030 others(31): Show |
34 | HG01081.hp1 HG01109.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1000+3520dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | ||||||
| chr13:28223871 | A | ATT | 11 | a0001c0001t0001g0026 a0001c0001t0001g0091 a0001c0001t0001g0096 others(8): Show |
11 | HG00735.hp2 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000+3519_1000+352 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | ||||||
| chr13:28223871 | AT | A | 73 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0062 others(70): Show |
73 | HG00438.hp2 HG00735.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.1000+3520delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | ||||||
| chr13:28223871 | ATT | A | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000+3519_1000+352 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | ||||||
| chr13:28223871 | ATTTTTTT others(1): Show |
A | 18 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0175 others(15): Show |
18 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1000+3513_1000+352 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | ||||||
| chr13:28223936 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1000+3558G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223936 | |||||||
| chr13:28223970 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+3592G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223970 | |||||||
| chr13:28224037 | T | A | 1 | a0001c0001t0013g0016 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1000+3659T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224037 | |||||||
| chr13:28224082 | A | G | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1000+3704A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224082 | |||||||
| chr13:28224171 | A | G | 58 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(55): Show |
58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1000+3793A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224171 | |||||||
| chr13:28224187 | G | A | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1000+3809G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224187 | |||||||
| chr13:28224187 | G | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+3809G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224187 | |||||||
| chr13:28224269 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1000+3891G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224269 | |||||||
| chr13:28224312 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1000+3934T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224312 | |||||||
| chr13:28224380 | G | C | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+4002G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224380 | |||||||
| chr13:28224543 | T | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+4165T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224543 | |||||||
| chr13:28224587 | G | T | 20 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0001t0001g0076 others(17): Show |
20 | HG00438.hp1 HG01109.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.1000+4209G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224587 | |||||||
| chr13:28224727 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1000+4349A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224727 | |||||||
| chr13:28225238 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+4860G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225238 | |||||||
| chr13:28225258 | C | T | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+4880C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225258 | |||||||
| chr13:28225398 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+5020T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225398 | |||||||
| chr13:28225437 | G | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+5059G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225437 | |||||||
| chr13:28225543 | A | G | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1000+5165A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225543 | |||||||
| chr13:28225747 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000+5369A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225747 | |||||||
| chr13:28225841 | A | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+5463A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225841 | |||||||
| chr13:28226186 | G | A | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1000+5808G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226186 | |||||||
| chr13:28226272 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1000+5894C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226272 | |||||||
| chr13:28226324 | C | A | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+5946C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226324 | |||||||
| chr13:28226630 | CTT | C | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000+6253_1000+625 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226630 | |||||||
| chr13:28226652 | T | C | 1 | a0001c0001t0009g0217 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1000+6274T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226652 | |||||||
| chr13:28227123 | A | G | 1 | a0001c0001t0004g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1000+6745A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227123 | |||||||
| chr13:28227479 | C | T | 35 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(32): Show |
35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1000+7101C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227479 | |||||||
| chr13:28227569 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1000+7191C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227569 | |||||||
| chr13:28227622 | T | C | 35 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(32): Show |
35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1000+7244T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227622 | |||||||
| chr13:28227731 | A | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+7353A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227731 | |||||||
| chr13:28227885 | T | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0169 |
2 | NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1000+7507T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227885 | |||||||
| chr13:28227977 | C | T | 58 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(55): Show |
58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1000+7599C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227977 | |||||||
| chr13:28228014 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
3 | HG02886.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1000+7636C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228014 | |||||||
| chr13:28228158 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1000+7780T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228158 | |||||||
| chr13:28228217 | G | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+7839G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228217 | |||||||
| chr13:28228333 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1000+7955T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228333 | |||||||
| chr13:28228497 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000+8119C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228497 | |||||||
| chr13:28228623 | CTAG | C | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+8250_1000+825 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28228623 | ||||||
| chr13:28228661 | T | G | 1 | a0001c0001t0006g0015 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1000+8283T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228661 | |||||||
| chr13:28228708 | C | A | 1 | a0001c0008t0001g0069 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1000+8330C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228708 | |||||||
| chr13:28228768 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+8390C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228768 | |||||||
| chr13:28228772 | A | G | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+8394A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228772 | |||||||
| chr13:28228887 | A | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+8509A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228887 | |||||||
| chr13:28228908 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1000+8530A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228908 | |||||||
| chr13:28228995 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1000+8617A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228995 | |||||||
| chr13:28229096 | A | G | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+8718A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229096 | |||||||
| chr13:28229263 | T | C | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1000+8885T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229263 | |||||||
| chr13:28229445 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1000+9067C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229445 | |||||||
| chr13:28229466 | C | T | 1 | a0001c0001t0053g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1000+9088C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229466 | |||||||
| chr13:28229499 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+9121T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229499 | |||||||
| chr13:28229570 | T | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1000+9192T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229570 | |||||||
| chr13:28229815 | G | A | 4 | a0001c0001t0004g0052 a0001c0001t0025g0203 a0001c0001t0038g0243 others(1): Show |
4 | HG01358.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+9437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229815 | |||||||
| chr13:28229909 | T | C | 1 | a0001c0001t0013g0016 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1000+9531T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229909 | |||||||
| chr13:28229999 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+9621C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229999 | |||||||
| chr13:28230054 | C | CT | 21 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0147 others(18): Show |
21 | HG00438.hp2 HG02080.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000+9687dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28230054 | ||||||
| chr13:28230054 | CT | C | 5 | a0001c0001t0001g0080 a0001c0001t0015g0250 a0001c0001t0029g0249 others(2): Show |
5 | HG02602.hp1 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+9687delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28230054 | ||||||
| chr13:28230272 | G | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000+9894G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230272 | |||||||
| chr13:28230352 | G | C | 3 | a0001c0001t0025g0203 a0001c0001t0038g0243 a0001c0007t0021g0151 |
3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1000+9974G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230352 | |||||||
| chr13:28230544 | T | A | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+10166T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230544 | |||||||
| chr13:28230787 | T | TTGAG | 147 | a0001c0001t0001g0067 a0001c0001t0001g0108 a0001c0001t0001g0129 others(144): Show |
147 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1000+10410_1000+10 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28230787 | ||||||
| chr13:28230996 | G | A | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+10618G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230996 | |||||||
| chr13:28231036 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0156 |
2 | NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1000+10658T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231036 | |||||||
| chr13:28231264 | A | G | 3 | a0001c0001t0025g0203 a0001c0001t0038g0243 a0001c0007t0021g0151 |
3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1000+10886A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231264 | |||||||
| chr13:28231344 | A | AGTT | 3 | a0001c0001t0039g0005 a0001c0001t0040g0004 a0001c0001t0041g0006 |
3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+10969_1000+10 others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28231344 | ||||||
| chr13:28231558 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+11180T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231558 | |||||||
| chr13:28231975 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+11597A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231975 | |||||||
| chr13:28232181 | C | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1000+11803C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232181 | |||||||
| chr13:28232287 | T | C | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1000+11909T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232287 | |||||||
| chr13:28232376 | C | T | 228 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(225): Show |
intron_variant | MODIFIER | c.1000+11998C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232376 | |||||||
| chr13:28232523 | C | T | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+12145C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232523 | |||||||
| chr13:28232598 | C | T | 1 | a0001c0001t0045g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1000+12220C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232598 | |||||||
| chr13:28232654 | A | G | 59 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1000+12276A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232654 | |||||||
| chr13:28233074 | A | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+12696A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233074 | |||||||
| chr13:28233112 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+12734A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233112 | |||||||
| chr13:28233208 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1000+12830A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233208 | |||||||
| chr13:28233268 | CT | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0039g0005 others(6): Show |
9 | HG02257.hp2 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000+12906delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28233268 | ||||||
| chr13:28233459 | G | T | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13081G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233459 | |||||||
| chr13:28233462 | T | C | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13084T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233462 | |||||||
| chr13:28233463 | C | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13085C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233463 | |||||||
| chr13:28233483 | T | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13105T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233483 | |||||||
| chr13:28233570 | A | C | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13192A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233570 | |||||||
| chr13:28233625 | T | C | 2 | a0001c0001t0013g0016 a0001c0001t0046g0035 |
2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1000+13247T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233625 | |||||||
| chr13:28233681 | A | T | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13303A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233681 | |||||||
| chr13:28233682 | T | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13304T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233682 | |||||||
| chr13:28233918 | G | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000+13540G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233918 | |||||||
| chr13:28234048 | T | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+13670T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234048 | |||||||
| chr13:28234163 | C | A | 1 | a0001c0001t0023g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1000+13785C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234163 | |||||||
| chr13:28234233 | C | G | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1000+13855C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234233 | |||||||
| chr13:28234275 | C | T | 1 | a0001c0001t0055g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1000+13897C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234275 | |||||||
| chr13:28234388 | T | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+14010T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234388 | |||||||
| chr13:28234437 | T | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+14059T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234437 | |||||||
| chr13:28234459 | G | A | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+14081G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234459 | |||||||
| chr13:28234465 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1000+14087T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234465 | |||||||
| chr13:28234490 | G | T | 3 | a0001c0003t0001g0138 a0001c0003t0004g0136 a0001c0003t0014g0084 |
3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1000+14112G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234490 | |||||||
| chr13:28234590 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+14212G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234590 | |||||||
| chr13:28234610 | A | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000+14232A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234610 | |||||||
| chr13:28234821 | A | C | 233 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1000+14443A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234821 | |||||||
| chr13:28234822 | T | C | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1000+14444T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234822 | |||||||
| chr13:28234968 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1000+14590A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234968 | |||||||
| chr13:28235620 | C | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1000+15242C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235620 | |||||||
| chr13:28235676 | C | G | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1000+15298C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235676 | |||||||
| chr13:28235682 | T | TACACACA others(5): Show |
1 | a0001c0001t0005g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1000+15306_1000+15 others(18): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | ||||||
| chr13:28235682 | T | TACACACA others(7): Show |
1 | a0001c0001t0007g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000+15317_1000+15 others(20): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | ||||||
| chr13:28235682 | T | TACACACA others(11): Show |
2 | a0001c0001t0005g0188 a0001c0001t0007g0177 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1000+15317_1000+15 others(24): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | ||||||
| chr13:28235682 | T | TACACACA others(13): Show |
2 | a0001c0001t0005g0172 a0001c0001t0005g0175 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1000+15317_1000+15 others(26): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | ||||||
| chr13:28235682 | T | TACACACA others(9): Show |
1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000+15313_1000+15 others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | ||||||
| chr13:28235688 | C | CACAT | 10 | a0001c0001t0002g0012 a0001c0001t0002g0216 a0001c0001t0002g0225 others(7): Show |
10 | HG01358.hp2 HG01361.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000+15313_1000+15 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235688 | ||||||
| chr13:28235690 | C | CAT | 55 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
55 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1000+15313_1000+15 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235690 | ||||||
| chr13:28235692 | C | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1000+15314C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235692 | |||||||
| chr13:28235696 | T | C | 76 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(73): Show |
76 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1000+15318T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235696 | |||||||
| chr13:28235696 | T | TAC | 103 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(100): Show |
103 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.1000+15344_1000+15 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACAC | 11 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(8): Show |
11 | HG00438.hp1 HG01175.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+15342_1000+15 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACAC | 21 | a0001c0001t0005g0179 a0001c0001t0005g0181 a0001c0001t0005g0182 others(18): Show |
21 | HG00597.hp2 HG00639.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000+15340_1000+15 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(1): Show |
11 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0183 others(8): Show |
11 | HG00099.hp1 HG01099.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000+15338_1000+15 others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(3): Show |
3 | a0001c0001t0011g0184 a0001c0001t0019g0185 a0001c0001t0038g0243 |
3 | HG02109.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1000+15336_1000+15 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(5): Show |
3 | a0001c0001t0008g0007 a0001c0001t0024g0228 a0001c0001t0031g0223 |
3 | HG02145.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1000+15334_1000+15 others(18): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(9): Show |
1 | a0001c0001t0010g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1000+15330_1000+15 others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(11): Show |
1 | a0001c0001t0010g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1000+15328_1000+15 others(24): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(13): Show |
4 | a0001c0001t0010g0121 a0001c0001t0010g0152 a0001c0001t0028g0125 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+15326_1000+15 others(26): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(17): Show |
1 | a0001c0001t0010g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1000+15322_1000+15 others(30): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235696 | T | TACACACA others(33): Show |
1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+15345_1000+15 others(46): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | ||||||
| chr13:28235722 | C | CACACACA others(11): Show |
1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+15345_1000+15 others(24): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235722 | ||||||
| chr13:28235722 | C | CACACACA others(3): Show |
1 | a0001c0001t0017g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1000+15345_1000+15 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235722 | ||||||
| chr13:28235722 | C | CACACAT | 4 | a0001c0001t0001g0157 a0001c0001t0004g0153 a0001c0001t0004g0158 others(1): Show |
4 | NA18941.hp1 NA18998.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+15345_1000+15 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235722 | ||||||
| chr13:28235724 | T | C | 103 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(100): Show |
103 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1000+15346T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235724 | |||||||
| chr13:28235726 | T | C | 16 | a0001c0001t0002g0225 a0001c0001t0005g0172 a0001c0001t0005g0173 others(13): Show |
16 | HG00639.hp2 HG01175.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1000+15348T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235726 | |||||||
| chr13:28235728 | T | C | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000+15350T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235728 | |||||||
| chr13:28235729 | A | T | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+15351A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235729 | |||||||
| chr13:28235768 | G | A | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1000+15390G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235768 | |||||||
| chr13:28235886 | A | AT | 6 | a0001c0001t0001g0140 a0001c0001t0004g0082 a0001c0001t0004g0107 others(3): Show |
6 | HG03098.hp2 HG03831.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+15525dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235886 | ||||||
| chr13:28235886 | AT | A | 73 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0213 others(70): Show |
73 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.1000+15525delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235886 | ||||||
| chr13:28236003 | A | ATTAC | 3 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0148 |
3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1000+15626_1000+15 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28236003 | ||||||
| chr13:28236103 | G | A | 106 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(103): Show |
106 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.1000+15725G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236103 | |||||||
| chr13:28236249 | G | A | 1 | a0001c0001t0017g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1000+15871G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236249 | |||||||
| chr13:28236285 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 |
3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1000+15907A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236285 | |||||||
| chr13:28236420 | T | C | 2 | a0001c0001t0013g0016 a0001c0001t0046g0035 |
2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1000+16042T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236420 | |||||||
| chr13:28236634 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1000+16256T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236634 | |||||||
| chr13:28236729 | A | G | 32 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(29): Show |
32 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1000+16351A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236729 | |||||||
| chr13:28237195 | AT | A | 220 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(217): Show |
220 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.1000+16829delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28237195 | ||||||
| chr13:28237195 | ATT | A | 23 | a0001c0001t0001g0118 a0001c0001t0002g0012 a0001c0001t0005g0117 others(20): Show |
23 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1000+16828_1000+16 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28237195 | ||||||
| chr13:28237219 | A | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+16841A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237219 | |||||||
| chr13:28237239 | A | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+16861A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237239 | |||||||
| chr13:28237535 | G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1000+17157G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237535 | |||||||
| chr13:28237742 | T | C | 73 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(70): Show |
73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.1000+17364T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237742 | |||||||
| chr13:28237887 | CAA | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+17510_1000+17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237887 | |||||||
| chr13:28238068 | C | A | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1000+17690C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238068 | |||||||
| chr13:28238075 | C | T | 2 | a0001c0001t0003g0215 a0001c0001t0003g0221 |
2 | NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1000+17697C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238075 | |||||||
| chr13:28238171 | A | G | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1000+17793A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238171 | |||||||
| chr13:28238186 | T | TGGAAGGC others(4): Show |
1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+17810_1000+17 others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28238186 | ||||||
| chr13:28238417 | C | A | 86 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(83): Show |
86 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.1001-17875C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238417 | |||||||
| chr13:28238446 | T | G | 20 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-17846T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238446 | |||||||
| chr13:28238541 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-17751A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238541 | |||||||
| chr13:28238562 | T | C | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-17730T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238562 | |||||||
| chr13:28238692 | C | T | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-17600C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238692 | |||||||
| chr13:28238693 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1001-17599G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238693 | |||||||
| chr13:28238762 | T | C | 1 | a0001c0001t0006g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1001-17530T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238762 | |||||||
| chr13:28238820 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1001-17472A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238820 | |||||||
| chr13:28238917 | T | G | 3 | a0001c0001t0003g0214 a0001c0001t0009g0189 a0001c0001t0047g0023 |
3 | HG01167.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1001-17375T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238917 | |||||||
| chr13:28238956 | G | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-17336G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238956 | |||||||
| chr13:28238987 | A | G | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-17305A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238987 | |||||||
| chr13:28239137 | A | AC | 17 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0076 others(14): Show |
17 | HG01099.hp2 HG01361.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1001-17147dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239137 | ||||||
| chr13:28239146 | A | C | 2 | a0001c0001t0005g0117 a0001c0009t0001g0064 |
2 | HG02056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1001-17146A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239146 | |||||||
| chr13:28239151 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1001-17141C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239151 | |||||||
| chr13:28239162 | A | AAC | 58 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0115 others(55): Show |
58 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1001-17105_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239162 | A | AACAC | 30 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0129 others(27): Show |
30 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1001-17107_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239162 | A | AACACAC | 87 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(84): Show |
87 | HG00099.hp2 HG01081.hp1 HG01099.hp2 others(84): Show |
intron_variant | MODIFIER | c.1001-17109_1001-17 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239162 | A | AACACACA others(1): Show |
29 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(26): Show |
29 | HG00438.hp1 HG00735.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1001-17111_1001-17 others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239162 | A | AACACACA others(3): Show |
6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-17113_1001-17 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239162 | AAC | A | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-17105_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239162 | AACAC | A | 7 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(4): Show |
7 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001-17107_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | ||||||
| chr13:28239192 | T | TGCACACA others(3): Show |
1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1001-17099_1001-17 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239192 | ||||||
| chr13:28239199 | A | ACG | 11 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(8): Show |
11 | HG00099.hp1 HG00597.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001-17091_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239199 | ||||||
| chr13:28239199 | A | ACGCG | 12 | a0001c0001t0005g0173 a0001c0001t0011g0184 a0001c0001t0011g0187 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1001-17090_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239199 | ||||||
| chr13:28239201 | G | GCA | 12 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0003g0214 others(9): Show |
12 | HG01167.hp2 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1001-17071_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | ||||||
| chr13:28239201 | G | GCGCA | 7 | a0001c0001t0005g0172 a0001c0001t0005g0175 a0001c0001t0005g0188 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-17090_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | ||||||
| chr13:28239201 | GCA | G | 5 | a0001c0001t0001g0058 a0001c0001t0050g0050 a0001c0001t0051g0099 others(2): Show |
5 | HG02132.hp1 HG02135.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-17071_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | ||||||
| chr13:28239201 | GCACA | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-17073_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | ||||||
| chr13:28239203 | A | G | 2 | a0001c0001t0007g0180 a0001c0001t0027g0150 |
2 | HG01099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1001-17089A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239203 | |||||||
| chr13:28239812 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1001-16480A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239812 | |||||||
| chr13:28239982 | T | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-16310T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239982 | |||||||
| chr13:28240233 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-16059A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240233 | |||||||
| chr13:28240450 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1001-15842A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240450 | |||||||
| chr13:28240518 | A | T | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-15774A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240518 | |||||||
| chr13:28240536 | C | T | 63 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0027 others(60): Show |
63 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.1001-15756C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240536 | |||||||
| chr13:28240876 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-15416C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240876 | |||||||
| chr13:28240986 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-15306G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240986 | |||||||
| chr13:28241011 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-15281A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241011 | |||||||
| chr13:28241032 | T | C | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-15260T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241032 | |||||||
| chr13:28241069 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1001-15223T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241069 | |||||||
| chr13:28241139 | T | C | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-15153T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241139 | |||||||
| chr13:28241635 | TATTA | T | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-14653_1001-14 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28241635 | ||||||
| chr13:28241777 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1001-14515C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241777 | |||||||
| chr13:28241878 | T | C | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-14414T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241878 | |||||||
| chr13:28241908 | T | TGACATAT others(25): Show |
1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1001-14383_1001-14 others(38): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28241908 | ||||||
| chr13:28241967 | C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-14325C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241967 | |||||||
| chr13:28241982 | G | C | 5 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-14310G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241982 | |||||||
| chr13:28242141 | G | A | 115 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(112): Show |
115 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1001-14151G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242141 | |||||||
| chr13:28242188 | T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-14104T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242188 | |||||||
| chr13:28242206 | A | G | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1001-14086A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242206 | |||||||
| chr13:28242240 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1001-14052A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242240 | |||||||
| chr13:28242267 | G | A | 44 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(41): Show |
44 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1001-14025G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242267 | |||||||
| chr13:28242283 | G | T | 22 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(19): Show |
22 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1001-14009G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242283 | |||||||
| chr13:28242326 | CTTGGTTG | C | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-13960_1001-13 others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28242326 | ||||||
| chr13:28242625 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-13667A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242625 | |||||||
| chr13:28242674 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1001-13618G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242674 | |||||||
| chr13:28242781 | A | G | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-13511A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242781 | |||||||
| chr13:28242913 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-13379C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242913 | |||||||
| chr13:28243025 | T | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-13267T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243025 | |||||||
| chr13:28243032 | C | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001-13260C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243032 | |||||||
| chr13:28243264 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-13028A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243264 | |||||||
| chr13:28243395 | G | C | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-12897G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243395 | |||||||
| chr13:28243400 | A | C | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-12892A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243400 | |||||||
| chr13:28243632 | C | T | 1 | a0001c0001t0009g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1001-12660C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243632 | |||||||
| chr13:28243684 | G | A | 1 | a0001c0001t0009g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1001-12608G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243684 | |||||||
| chr13:28243743 | T | C | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-12549T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243743 | |||||||
| chr13:28243788 | C | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1001-12504C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243788 | |||||||
| chr13:28243846 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-12446G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243846 | |||||||
| chr13:28243860 | T | C | 64 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0026 others(61): Show |
64 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.1001-12432T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243860 | |||||||
| chr13:28244163 | G | T | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-12129G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244163 | |||||||
| chr13:28244273 | C | T | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1001-12019C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244273 | |||||||
| chr13:28244511 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1001-11781T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244511 | |||||||
| chr13:28244579 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0156 |
2 | NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1001-11713C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244579 | |||||||
| chr13:28244581 | G | T | 2 | a0001c0003t0001g0138 a0001c0003t0004g0136 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1001-11711G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244581 | |||||||
| chr13:28244604 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0004g0082 |
2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1001-11688A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244604 | |||||||
| chr13:28244682 | T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-11610T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244682 | |||||||
| chr13:28244759 | CAGT | C | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-11526_1001-11 others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28244759 | ||||||
| chr13:28244798 | T | C | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-11494T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244798 | |||||||
| chr13:28244910 | G | A | 1 | a0002c0005t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1001-11382G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244910 | |||||||
| chr13:28245115 | G | C | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1001-11177G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245115 | |||||||
| chr13:28245370 | C | T | 14 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.1001-10922C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245370 | |||||||
| chr13:28245391 | C | CT | 14 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(11): Show |
14 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1001-10890dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28245391 | ||||||
| chr13:28245391 | C | CTT | 20 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-10891_1001-10 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28245391 | ||||||
| chr13:28245721 | AC | A | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-10570delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245721 | |||||||
| chr13:28245767 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-10525C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245767 | |||||||
| chr13:28245973 | A | G | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-10319A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245973 | |||||||
| chr13:28246389 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-9903A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246389 | |||||||
| chr13:28246473 | C | A | 105 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(102): Show |
105 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.1001-9819C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246473 | |||||||
| chr13:28246473 | C | T | 142 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0213 others(139): Show |
142 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1001-9819C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246473 | |||||||
| chr13:28246638 | A | G | 1 | a0001c0001t0009g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1001-9654A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246638 | |||||||
| chr13:28246658 | T | C | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-9634T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246658 | |||||||
| chr13:28246796 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0004g0082 |
2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1001-9496A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246796 | |||||||
| chr13:28246856 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-9436C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246856 | |||||||
| chr13:28246900 | C | T | 1 | a0001c0001t0053g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1001-9392C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246900 | |||||||
| chr13:28247136 | T | C | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-9156T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247136 | |||||||
| chr13:28247180 | C | CT | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-9106dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28247180 | ||||||
| chr13:28247261 | C | A | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-9031C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247261 | |||||||
| chr13:28247267 | G | C | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-9025G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247267 | |||||||
| chr13:28247343 | G | A | 1 | a0001c0001t0003g0010 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1001-8949G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247343 | |||||||
| chr13:28247394 | C | G | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1001-8898C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247394 | |||||||
| chr13:28247416 | G | T | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-8876G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247416 | |||||||
| chr13:28247603 | A | G | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1001-8689A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247603 | |||||||
| chr13:28247816 | C | T | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1001-8476C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247816 | |||||||
| chr13:28247822 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1001-8470C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247822 | |||||||
| chr13:28247974 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-8318A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247974 | |||||||
| chr13:28248127 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-8165T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248127 | |||||||
| chr13:28248242 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1001-8050G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248242 | |||||||
| chr13:28248383 | G | C | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-7909G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248383 | |||||||
| chr13:28248517 | G | A | 1 | a0001c0001t0048g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1001-7775G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248517 | |||||||
| chr13:28248520 | CT | C | 246 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.1001-7762delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28248520 | ||||||
| chr13:28248979 | C | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-7313C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248979 | |||||||
| chr13:28248985 | T | G | 1 | a0001c0001t0004g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1001-7307T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248985 | |||||||
| chr13:28249095 | A | T | 92 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(89): Show |
92 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.1001-7197A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249095 | |||||||
| chr13:28249133 | A | G | 2 | a0001c0001t0010g0121 a0001c0001t0010g0122 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1001-7159A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249133 | |||||||
| chr13:28249140 | A | G | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001-7152A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249140 | |||||||
| chr13:28249157 | T | C | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-7135T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249157 | |||||||
| chr13:28249356 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1001-6936T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249356 | |||||||
| chr13:28249439 | A | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-6853A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249439 | |||||||
| chr13:28249518 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-6774G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249518 | |||||||
| chr13:28249531 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-6761C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249531 | |||||||
| chr13:28249532 | T | G | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001-6760T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249532 | |||||||
| chr13:28249741 | C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-6551C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249741 | |||||||
| chr13:28249848 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1001-6444A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249848 | |||||||
| chr13:28250056 | T | C | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-6236T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250056 | |||||||
| chr13:28250076 | G | A | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1001-6216G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250076 | |||||||
| chr13:28250129 | A | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1001-6163A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250129 | |||||||
| chr13:28250183 | C | T | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-6109C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250183 | |||||||
| chr13:28250194 | C | G | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-6098C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250194 | |||||||
| chr13:28250201 | C | CT | 10 | a0001c0001t0001g0092 a0001c0001t0010g0121 a0001c0001t0010g0122 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001-6077dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28250201 | ||||||
| chr13:28250201 | C | CTT | 6 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-6078_1001-607 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28250201 | ||||||
| chr13:28250201 | C | CTTT | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-6079_1001-607 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28250201 | ||||||
| chr13:28250203 | T | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0169 |
2 | NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1001-6089T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250203 | |||||||
| chr13:28250314 | G | T | 105 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(102): Show |
105 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.1001-5978G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250314 | |||||||
| chr13:28250338 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1001-5954G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250338 | |||||||
| chr13:28250390 | G | A | 103 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(100): Show |
103 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.1001-5902G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250390 | |||||||
| chr13:28250590 | C | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-5702C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250590 | |||||||
| chr13:28250618 | C | T | 119 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(116): Show |
119 | HG00099.hp2 HG00438.hp1 HG00735.hp1 others(116): Show |
intron_variant | MODIFIER | c.1001-5674C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250618 | |||||||
| chr13:28250782 | G | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001-5510G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250782 | |||||||
| chr13:28250810 | G | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0014g0113 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-5482G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250810 | |||||||
| chr13:28250815 | C | T | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1001-5477C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250815 | |||||||
| chr13:28251371 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1001-4921G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251371 | |||||||
| chr13:28251479 | G | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-4813G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251479 | |||||||
| chr13:28251574 | C | A | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1001-4718C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251574 | |||||||
| chr13:28251612 | C | T | 1 | a0001c0001t0005g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1001-4680C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251612 | |||||||
| chr13:28251618 | C | T | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-4674C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251618 | |||||||
| chr13:28251642 | A | G | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-4650A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251642 | |||||||
| chr13:28251701 | G | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-4591G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251701 | |||||||
| chr13:28251772 | C | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-4520C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251772 | |||||||
| chr13:28251793 | CT | C | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-4498delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251793 | |||||||
| chr13:28251801 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1001-4491G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251801 | |||||||
| chr13:28251871 | G | GGTTT | 8 | a0001c0001t0001g0061 a0001c0001t0011g0184 a0001c0001t0019g0185 others(5): Show |
8 | HG01109.hp1 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1001-4418_1001-441 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28251871 | ||||||
| chr13:28251875 | G | GGTTT | 123 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1001-4395_1001-439 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28251875 | ||||||
| chr13:28251875 | G | GGTTTGTT others(1): Show |
6 | a0001c0001t0001g0119 a0001c0001t0005g0172 a0001c0001t0005g0173 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-4399_1001-439 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28251875 | ||||||
| chr13:28251875 | G | T | 14 | a0001c0001t0001g0061 a0001c0001t0011g0184 a0001c0001t0011g0187 others(11): Show |
14 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-4417G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251875 | |||||||
| chr13:28251902 | T | C | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1001-4390T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251902 | |||||||
| chr13:28252031 | G | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-4261G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252031 | |||||||
| chr13:28252116 | G | C | 1 | a0001c0001t0003g0166 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1001-4176G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252116 | |||||||
| chr13:28252184 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1001-4108G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252184 | |||||||
| chr13:28252188 | C | CT | 5 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0029g0249 others(2): Show |
5 | HG01175.hp2 HG03098.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-4082dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | ||||||
| chr13:28252188 | CT | C | 33 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(30): Show |
33 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1001-4082delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | ||||||
| chr13:28252188 | CTT | C | 80 | a0001c0001t0001g0213 a0001c0001t0002g0011 a0001c0001t0002g0012 others(77): Show |
80 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.1001-4083_1001-408 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | ||||||
| chr13:28252188 | CTTT | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0143 a0001c0001t0002g0144 others(7): Show |
10 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001-4084_1001-408 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | ||||||
| chr13:28252252 | C | G | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1001-4040C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252252 | |||||||
| chr13:28252299 | G | A | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1001-3993G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252299 | |||||||
| chr13:28252412 | T | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-3880T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252412 | |||||||
| chr13:28252478 | T | TA | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001-3813dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252478 | ||||||
| chr13:28252761 | A | G | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-3531A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252761 | |||||||
| chr13:28252828 | A | G | 6 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-3464A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252828 | |||||||
| chr13:28252846 | A | G | 94 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(91): Show |
94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.1001-3446A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252846 | |||||||
| chr13:28252934 | G | A | 1 | a0001c0001t0004g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1001-3358G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252934 | |||||||
| chr13:28252959 | C | T | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001-3333C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252959 | |||||||
| chr13:28253301 | TA | T | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-2989delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28253301 | ||||||
| chr13:28253712 | C | A | 1 | a0001c0001t0010g0152 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1001-2580C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28253712 | |||||||
| chr13:28253713 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-2579G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28253713 | |||||||
| chr13:28253715 | TC | T | 94 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(91): Show |
94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.1001-2575delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28253715 | ||||||
| chr13:28253785 | T | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-2507T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28253785 | |||||||
| chr13:28254055 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-2237A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254055 | |||||||
| chr13:28254080 | G | A | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-2212G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254080 | |||||||
| chr13:28254135 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-2157C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254135 | |||||||
| chr13:28254279 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1001-2013T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254279 | |||||||
| chr13:28254416 | T | C | 20 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-1876T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254416 | |||||||
| chr13:28254705 | A | AT | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-1579dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28254705 | ||||||
| chr13:28254756 | A | G | 4 | a0001c0001t0006g0013 a0001c0001t0006g0015 a0001c0001t0006g0019 others(1): Show |
4 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1536A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254756 | |||||||
| chr13:28254975 | C | T | 72 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.1001-1317C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254975 | |||||||
| chr13:28255085 | T | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-1207T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255085 | |||||||
| chr13:28255106 | C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-1186C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255106 | |||||||
| chr13:28255139 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1001-1153T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255139 | |||||||
| chr13:28255298 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1001-994A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255298 | |||||||
| chr13:28255335 | T | C | 3 | a0001c0001t0009g0192 a0001c0001t0009g0199 a0001c0001t0009g0217 |
3 | NA18943.hp2 NA18981.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1001-957T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255335 | |||||||
| chr13:28255527 | C | T | 95 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(92): Show |
95 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(92): Show |
intron_variant | MODIFIER | c.1001-765C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255527 | |||||||
| chr13:28255855 | G | A | 4 | a0001c0001t0005g0179 a0001c0001t0005g0206 a0001c0001t0007g0178 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255855 | |||||||
| chr13:28255995 | T | A | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-297T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255995 | |||||||
| chr13:28256275 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0004g0043 |
2 | NA18956.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1001-17T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28256275 | |||||||
| chr13:28256281 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1001-11A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28256281 | |||||||
| chr13:28256860 | T | G | 98 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(95): Show |
98 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(95): Show |
intron_variant | MODIFIER | c.1248+321T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28256860 | |||||||
| chr13:28256861 | A | C | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+322A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28256861 | |||||||
| chr13:28257045 | A | G | 1 | a0003c0006t0015g0251 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1248+506A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257045 | |||||||
| chr13:28257104 | A | G | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1248+565A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257104 | |||||||
| chr13:28257115 | A | T | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+576A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257115 | |||||||
| chr13:28257134 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1248+595G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257134 | |||||||
| chr13:28257171 | T | C | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+632T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257171 | |||||||
| chr13:28257278 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248+739G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257278 | |||||||
| chr13:28257318 | G | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+779G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257318 | |||||||
| chr13:28257505 | G | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1248+966G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257505 | |||||||
| chr13:28257559 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1248+1020A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257559 | |||||||
| chr13:28257639 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1248+1100A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257639 | |||||||
| chr13:28257687 | T | TATAAATA others(22): Show |
11 | a0001c0001t0004g0052 a0001c0001t0006g0013 a0001c0001t0006g0014 others(8): Show |
11 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+1151_1248+117 others(33): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257687 | ||||||
| chr13:28257687 | T | TATAAATA others(51): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0045g0051 |
3 | HG01346.hp2 HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1248+1179_1248+118 others(62): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257687 | ||||||
| chr13:28257690 | A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1248+1169_1248+119 others(33): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257690 | ||||||
| chr13:28257699 | TTA | T | 2 | a0001c0001t0002g0222 a0001c0001t0003g0009 |
2 | HG00438.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1248+1168_1248+116 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257699 | ||||||
| chr13:28257701 | A | ATATATAT others(20): Show |
3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1248+1170_1248+119 others(31): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257701 | ||||||
| chr13:28257706 | T | TATTATAT others(24): Show |
1 | a0001c0001t0007g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1248+1180_1248+121 others(35): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257706 | ||||||
| chr13:28257709 | T | A | 4 | a0001c0001t0005g0172 a0001c0001t0005g0175 a0001c0001t0005g0188 others(1): Show |
4 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+1170T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257709 | |||||||
| chr13:28257721 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1248+1222_1248+126 others(43): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257721 | ||||||
| chr13:28257721 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248+1222_1248+126 others(43): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257721 | ||||||
| chr13:28257727 | ATTATATA others(44): Show |
A | 2 | a0001c0001t0005g0182 a0001c0001t0007g0180 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1190_1248+124 others(55): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257727 | ||||||
| chr13:28257737 | A | T | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1198A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257737 | |||||||
| chr13:28257758 | A | ATATATAA others(3): Show |
1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1219_1248+122 others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257758 | |||||||
| chr13:28257760 | T | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1221T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257760 | |||||||
| chr13:28257762 | A | T | 75 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(72): Show |
75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.1248+1223A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257762 | |||||||
| chr13:28257767 | T | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1228T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257767 | |||||||
| chr13:28257769 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1248+1230A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257769 | |||||||
| chr13:28257775 | A | T | 3 | a0001c0001t0002g0197 a0001c0001t0020g0194 a0001c0001t0020g0202 |
3 | NA18991.hp1 NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1248+1236A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257775 | |||||||
| chr13:28257783 | T | A | 2 | a0001c0001t0005g0182 a0001c0001t0007g0180 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1244T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257783 | |||||||
| chr13:28257794 | A | T | 2 | a0001c0001t0005g0182 a0001c0001t0007g0180 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1255A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257794 | |||||||
| chr13:28257795 | T | A | 2 | a0001c0001t0005g0182 a0001c0001t0007g0180 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1256T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257795 | |||||||
| chr13:28257824 | A | G | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+1285A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257824 | |||||||
| chr13:28257851 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1248+1312C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257851 | |||||||
| chr13:28257935 | C | G | 96 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(93): Show |
96 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.1248+1396C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257935 | |||||||
| chr13:28258085 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1248+1546C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258085 | |||||||
| chr13:28258145 | C | T | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1248+1606C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258145 | |||||||
| chr13:28258169 | A | G | 2 | a0001c0001t0023g0171 a0001c0001t0024g0228 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1248+1630A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258169 | |||||||
| chr13:28258239 | G | C | 93 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(90): Show |
93 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.1248+1700G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258239 | |||||||
| chr13:28258397 | A | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1858A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258397 | |||||||
| chr13:28258662 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1249-1785C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258662 | |||||||
| chr13:28258850 | A | G | 74 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1249-1597A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258850 | |||||||
| chr13:28259006 | C | T | 74 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1249-1441C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259006 | |||||||
| chr13:28259047 | A | G | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1249-1400A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259047 | |||||||
| chr13:28259064 | C | T | 1 | a0001c0001t0004g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1249-1383C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259064 | |||||||
| chr13:28259131 | A | AT | 43 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(40): Show |
43 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1249-1302dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28259131 | ||||||
| chr13:28259131 | A | ATT | 5 | a0001c0002t0012g0162 a0001c0002t0012g0209 a0001c0002t0012g0211 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-1303_1249-130 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28259131 | ||||||
| chr13:28259135 | T | C | 74 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1249-1312T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259135 | |||||||
| chr13:28259166 | C | G | 2 | a0001c0001t0005g0179 a0001c0001t0007g0178 |
2 | HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1249-1281C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259166 | |||||||
| chr13:28259173 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1249-1274G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259173 | |||||||
| chr13:28259235 | C | G | 63 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0027 others(60): Show |
63 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.1249-1212C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259235 | |||||||
| chr13:28259273 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1249-1174G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259273 | |||||||
| chr13:28259300 | G | GT | 5 | a0001c0001t0013g0016 a0001c0001t0013g0127 a0001c0001t0013g0128 others(2): Show |
5 | HG00099.hp2 HG03225.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-1139dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28259300 | ||||||
| chr13:28259301 | T | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1249-1146T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259301 | |||||||
| chr13:28259307 | T | C | 2 | a0001c0001t0002g0193 a0001c0001t0035g0200 |
2 | NA18974.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1249-1140T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259307 | |||||||
| chr13:28259430 | C | G | 1 | a0001c0001t0004g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1249-1017C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259430 | |||||||
| chr13:28259482 | T | C | 4 | a0001c0001t0011g0187 a0001c0001t0011g0242 a0001c0001t0019g0238 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-965T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259482 | |||||||
| chr13:28259641 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1249-806A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259641 | |||||||
| chr13:28259799 | C | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-648C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259799 | |||||||
| chr13:28259879 | C | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-568C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259879 | |||||||
| chr13:28259955 | A | G | 2 | a0001c0001t0005g0206 a0001c0001t0030g0161 |
2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1249-492A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259955 | |||||||
| chr13:28260119 | G | A | 11 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(8): Show |
11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1249-328G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28260119 | |||||||
| chr13:28260227 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1249-220T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28260227 | |||||||
| chr13:28260648 | T | C | 1 | a0001c0001t0013g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1353+97T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260648 | |||||||
| chr13:28260717 | CT | C | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353+170delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 28260717 | ||||||
| chr13:28260723 | A | G | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353+172A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260723 | |||||||
| chr13:28260797 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1353+246T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260797 | |||||||
| chr13:28260988 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1354-413G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260988 | |||||||
| chr13:28261165 | C | T | 70 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(67): Show |
70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1354-236C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261165 | |||||||
| chr13:28261230 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1354-171C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261230 | |||||||
| chr13:28261268 | A | C | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1354-133A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261268 | |||||||
| chr13:28261325 | G | A | 93 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(90): Show |
93 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.1354-76G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261325 | |||||||
| chr13:28261339 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1354-62A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261339 | |||||||
| chr13:28261390 | T | TC | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1354-11_1354-10ins others(1): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261390 | |||||||
| chr13:28261510 | C | T | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1411+52C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261510 | |||||||
| chr13:28261511 | G | T | 1 | a0001c0001t0005g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1411+53G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261511 | |||||||
| chr13:28261546 | T | C | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+88T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261546 | |||||||
| chr13:28261832 | C | CA | 139 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1411+393dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28261832 | ||||||
| chr13:28261832 | C | CAA | 8 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0101 others(5): Show |
8 | HG01433.hp1 HG02083.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411+392_1411+393d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28261832 | ||||||
| chr13:28261849 | AAAG | A | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1411+392_1411+394d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261849 | |||||||
| chr13:28262068 | G | A | 4 | a0001c0001t0005g0179 a0001c0001t0005g0206 a0001c0001t0007g0178 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+610G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262068 | |||||||
| chr13:28262070 | C | A | 70 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(67): Show |
70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1411+612C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262070 | |||||||
| chr13:28262136 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0156 |
2 | NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1411+678T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262136 | |||||||
| chr13:28262180 | A | G | 1 | a0001c0001t0006g0132 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1411+722A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262180 | |||||||
| chr13:28262194 | A | T | 3 | a0001c0001t0002g0197 a0001c0001t0020g0194 a0001c0001t0020g0202 |
3 | NA18991.hp1 NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1411+736A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262194 | |||||||
| chr13:28262239 | T | A | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411+781T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262239 | |||||||
| chr13:28262255 | C | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1411+797C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262255 | |||||||
| chr13:28262422 | G | A | 69 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(66): Show |
69 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1411+964G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262422 | |||||||
| chr13:28262713 | CA | C | 105 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(102): Show |
105 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.1411+1258delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28262713 | ||||||
| chr13:28263090 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411+1632G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263090 | |||||||
| chr13:28263103 | A | G | 1 | a0001c0001t0023g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1411+1645A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263103 | |||||||
| chr13:28263159 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0004g0082 |
2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1411+1701G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263159 | |||||||
| chr13:28263334 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1411+1876A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263334 | |||||||
| chr13:28263835 | G | A | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1411+2377G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263835 | |||||||
| chr13:28263853 | A | AT | 6 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+2402dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28263853 | ||||||
| chr13:28263903 | C | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411+2445C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263903 | |||||||
| chr13:28263951 | G | A | 3 | a0001c0001t0008g0245 a0001c0001t0008g0246 a0001c0001t0008g0247 |
3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1411+2493G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263951 | |||||||
| chr13:28263970 | C | T | 2 | a0001c0001t0006g0014 a0001c0001t0045g0051 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1411+2512C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263970 | |||||||
| chr13:28264033 | T | G | 2 | a0001c0001t0031g0223 a0001c0001t0047g0023 |
2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1411+2575T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264033 | |||||||
| chr13:28264173 | ATAAT | A | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-2539_1412-253 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28264173 | ||||||
| chr13:28264289 | A | G | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1412-2426A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264289 | |||||||
| chr13:28264355 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1412-2360A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264355 | |||||||
| chr13:28264391 | T | G | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-2324T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264391 | |||||||
| chr13:28264499 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1412-2216G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264499 | |||||||
| chr13:28264658 | C | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG02040.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1412-2057C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264658 | |||||||
| chr13:28264771 | G | C | 31 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(28): Show |
31 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-1944G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264771 | |||||||
| chr13:28264835 | G | T | 1 | a0001c0001t0005g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1412-1880G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264835 | |||||||
| chr13:28264931 | T | C | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1412-1784T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264931 | |||||||
| chr13:28264940 | C | T | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-1775C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264940 | |||||||
| chr13:28265012 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1412-1703G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265012 | |||||||
| chr13:28265065 | C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1412-1650C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265065 | |||||||
| chr13:28265174 | G | A | 2 | a0001c0001t0006g0017 a0001c0001t0006g0020 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-1541G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265174 | |||||||
| chr13:28265189 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1412-1526A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265189 | |||||||
| chr13:28265719 | GT | G | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(8): Show |
11 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-971delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | ||||||
| chr13:28265719 | GTTTTTTT others(317): Show |
G | 11 | a0001c0001t0001g0139 a0001c0001t0004g0059 a0001c0001t0009g0160 others(8): Show |
11 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-984_1412-661d others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | ||||||
| chr13:28265719 | GTTTTTTT others(318): Show |
G | 155 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1412-985_1412-661d others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | ||||||
| chr13:28265719 | GTTTTTTT others(319): Show |
G | 67 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(64): Show |
67 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1412-986_1412-661d others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | ||||||
| chr13:28266036 | GT | G | 13 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0006g0013 others(10): Show |
13 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-661delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28266036 | ||||||
| chr13:28266084 | G | A | 7 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(4): Show |
7 | NA18944.hp1 NA18981.hp1 NA19074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-631G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28266084 | |||||||
| chr13:28267042 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1574-53A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 10/18 | chr13 | 28267042 | |||||||
| chr13:28267262 | C | A | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1691-38C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 11/18 | chr13 | 28267262 | |||||||
| chr13:28267492 | C | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792+91C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267492 | |||||||
| chr13:28267551 | C | T | 2 | a0001c0001t0005g0207 a0001c0001t0007g0237 |
2 | NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1792+150C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267551 | |||||||
| chr13:28267628 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1792+227G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267628 | |||||||
| chr13:28267703 | A | G | 1 | a0001c0001t0004g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1792+302A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267703 | |||||||
| chr13:28267876 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1792+475G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267876 | |||||||
| chr13:28267925 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+524G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267925 | |||||||
| chr13:28267927 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+526T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267927 | |||||||
| chr13:28267928 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+527G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267928 | |||||||
| chr13:28267932 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+531G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267932 | |||||||
| chr13:28267935 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+534A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267935 | |||||||
| chr13:28267936 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+535A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267936 | |||||||
| chr13:28267938 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+537A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267938 | |||||||
| chr13:28267939 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+538A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267939 | |||||||
| chr13:28267940 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+539G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267940 | |||||||
| chr13:28268171 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1792+770C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268171 | |||||||
| chr13:28268319 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+918A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268319 | |||||||
| chr13:28268485 | G | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1792+1084G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268485 | |||||||
| chr13:28268703 | A | G | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1792+1302A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268703 | |||||||
| chr13:28268782 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+1381A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268782 | |||||||
| chr13:28268813 | CT | C | 4 | a0001c0001t0001g0089 a0001c0001t0015g0250 a0001c0001t0029g0249 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792+1421delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 28268813 | ||||||
| chr13:28269284 | A | C | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1793-1417A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269284 | |||||||
| chr13:28269385 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1793-1316C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269385 | |||||||
| chr13:28269626 | CTT | C | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1793-1074_1793-107 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269626 | |||||||
| chr13:28269674 | C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1793-1027C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269674 | |||||||
| chr13:28269702 | T | C | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1793-999T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269702 | |||||||
| chr13:28269711 | G | A | 3 | a0001c0003t0001g0138 a0001c0003t0004g0136 a0001c0003t0014g0084 |
3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1793-990G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269711 | |||||||
| chr13:28269776 | T | C | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1793-925T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269776 | |||||||
| chr13:28270019 | G | T | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1793-682G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270019 | |||||||
| chr13:28270024 | T | C | 71 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1793-677T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270024 | |||||||
| chr13:28270068 | A | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0014g0113 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1793-633A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270068 | |||||||
| chr13:28270258 | A | G | 8 | a0001c0001t0002g0115 a0001c0001t0002g0164 a0001c0001t0002g0168 others(5): Show |
8 | HG02071.hp1 HG02523.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1793-443A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270258 | |||||||
| chr13:28270571 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1793-130A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270571 | |||||||
| chr13:28270590 | C | A | 4 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0023g0171 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-111C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270590 | |||||||
| chr13:28270674 | C | A | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1793-27C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270674 | |||||||
| chr13:28270910 | C | T | 1 | a0001c0001t0022g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1958+44C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28270910 | |||||||
| chr13:28271054 | T | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+188T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271054 | |||||||
| chr13:28271074 | G | A | 11 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(8): Show |
11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1958+208G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271074 | |||||||
| chr13:28271074 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1958+208G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271074 | |||||||
| chr13:28271129 | A | G | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1958+263A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271129 | |||||||
| chr13:28271261 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1958+395A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271261 | |||||||
| chr13:28271448 | T | A | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1959-533T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271448 | |||||||
| chr13:28271461 | A | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1959-520A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271461 | |||||||
| chr13:28271574 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1959-407C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271574 | |||||||
| chr13:28271591 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1959-390A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271591 | |||||||
| chr13:28271784 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1959-197A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271784 | |||||||
| chr13:28271848 | G | A | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1959-133G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271848 | |||||||
| chr13:28271855 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1959-126A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271855 | |||||||
| chr13:28271934 | T | A | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1959-47T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271934 | |||||||
| chr13:28272270 | T | C | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2049+199T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28272270 | |||||||
| chr13:28272381 | C | T | 2 | a0001c0001t0010g0121 a0001c0001t0010g0122 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2049+310C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28272381 | |||||||
| chr13:28272572 | C | CT | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2049+515dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 28272572 | ||||||
| chr13:28272998 | C | T | 60 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0027 others(57): Show |
60 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.2049+927C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28272998 | |||||||
| chr13:28273275 | C | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2049+1204C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273275 | |||||||
| chr13:28273342 | C | T | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2049+1271C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273342 | |||||||
| chr13:28273377 | A | G | 131 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(128): Show |
131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.2049+1306A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273377 | |||||||
| chr13:28273505 | G | A | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2049+1434G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273505 | |||||||
| chr13:28273555 | C | T | 2 | a0001c0001t0001g0072 a0001c0009t0001g0064 |
2 | HG02056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2049+1484C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273555 | |||||||
| chr13:28273600 | C | CA | 11 | a0001c0001t0005g0207 a0001c0001t0007g0237 a0001c0001t0010g0121 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.2049+1541dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 28273600 | ||||||
| chr13:28273801 | G | A | 1 | a0001c0001t0009g0217 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2049+1730G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273801 | |||||||
| chr13:28273859 | T | C | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2049+1788T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273859 | |||||||
| chr13:28274256 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2049+2185C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274256 | |||||||
| chr13:28274332 | G | C | 1 | a0001c0001t0007g0237 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2049+2261G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274332 | |||||||
| chr13:28274522 | C | T | 10 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0201 others(7): Show |
10 | HG02080.hp1 HG02135.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2049+2451C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274522 | |||||||
| chr13:28274578 | C | G | 72 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.2049+2507C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274578 | |||||||
| chr13:28274627 | C | T | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2049+2556C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274627 | |||||||
| chr13:28274742 | A | G | 1 | a0001c0001t0030g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2050-2495A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274742 | |||||||
| chr13:28275208 | C | G | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050-2029C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275208 | |||||||
| chr13:28275539 | A | G | 11 | a0001c0001t0011g0184 a0001c0001t0011g0187 a0001c0001t0011g0242 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2050-1698A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275539 | |||||||
| chr13:28275625 | G | A | 1 | a0001c0001t0056g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2050-1612G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275625 | |||||||
| chr13:28275784 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0003g0003 others(1): Show |
4 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050-1453A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275784 | |||||||
| chr13:28275832 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0090 |
2 | HG01167.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2050-1405T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275832 | |||||||
| chr13:28275979 | TA | T | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2050-1257delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275979 | |||||||
| chr13:28276073 | C | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2050-1164C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276073 | |||||||
| chr13:28276430 | A | G | 72 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.2050-807A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276430 | |||||||
| chr13:28276575 | G | A | 1 | a0001c0001t0004g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2050-662G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276575 | |||||||
| chr13:28276699 | C | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2050-538C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276699 | |||||||
| chr13:28277120 | G | A | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2050-117G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28277120 | |||||||
| chr13:28277150 | C | T | 1 | a0001c0004t0004g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2050-87C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28277150 | |||||||
| chr13:28277195 | G | A | 127 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(124): Show |
127 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.2050-42G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28277195 | |||||||
| chr13:28277585 | G | A | 104 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(101): Show |
104 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.2189+209G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277585 | |||||||
| chr13:28277680 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+304A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277680 | |||||||
| chr13:28277709 | C | T | 14 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.2189+333C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277709 | |||||||
| chr13:28277716 | A | G | 74 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.2189+340A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277716 | |||||||
| chr13:28278119 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2189+743T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278119 | |||||||
| chr13:28278435 | A | G | 1 | a0001c0001t0015g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2189+1059A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278435 | |||||||
| chr13:28278636 | A | T | 1 | a0001c0001t0002g0144 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2189+1260A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278636 | |||||||
| chr13:28278639 | T | A | 1 | a0001c0001t0002g0144 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2189+1263T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278639 | |||||||
| chr13:28278644 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0106 a0001c0001t0001g0135 |
3 | HG02523.hp2 NA18747.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2189+1268C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278644 | |||||||
| chr13:28278794 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2189+1418G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278794 | |||||||
| chr13:28279094 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2190-1318A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279094 | |||||||
| chr13:28279572 | A | T | 74 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.2190-840A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279572 | |||||||
| chr13:28279858 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2190-554G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279858 | |||||||
| chr13:28279941 | A | C | 1 | a0001c0001t0004g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2190-471A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279941 | |||||||
| chr13:28279994 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2190-418T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279994 | |||||||
| chr13:28280010 | G | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
3 | HG02886.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2190-402G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28280010 | |||||||
| chr13:28280555 | A | AT | 122 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.2319+38dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | ||||||
| chr13:28280555 | A | ATT | 32 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0090 others(29): Show |
32 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.2319+37_2319+38dup others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | ||||||
| chr13:28280555 | A | ATTT | 6 | a0001c0001t0005g0182 a0001c0001t0007g0116 a0001c0001t0007g0180 others(3): Show |
6 | HG03098.hp2 HG03225.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.2319+36_2319+38dup others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | ||||||
| chr13:28280555 | A | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2319+14A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | chr13 | 28280555 | |||||||
| chr13:28280555 | AT | A | 14 | a0001c0001t0002g0011 a0001c0001t0002g0036 a0001c0001t0002g0037 others(11): Show |
14 | HG02040.hp1 HG02083.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.2319+38delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | ||||||
| chr13:28280884 | T | C | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2319+343T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | chr13 | 28280884 | |||||||
| chr13:28280948 | G | A | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2320-367G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | chr13 | 28280948 | |||||||
| chr13:28281466 | A | G | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+87A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281466 | |||||||
| chr13:28281469 | AAG | A | 19 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00438.hp1 HG01109.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2384+94_2384+95del others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28281469 | ||||||
| chr13:28281648 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2384+269A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281648 | |||||||
| chr13:28281662 | A | G | 1 | a0001c0001t0034g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2384+283A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281662 | |||||||
| chr13:28281723 | A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2384+344A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281723 | |||||||
| chr13:28281760 | A | C | 1 | a0001c0001t0006g0132 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2384+381A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281760 | |||||||
| chr13:28281766 | CT | C | 155 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(152): Show |
155 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.2384+407delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28281766 | ||||||
| chr13:28281766 | CTT | C | 71 | a0001c0001t0001g0071 a0001c0001t0001g0078 a0001c0001t0001g0213 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2384+406_2384+407d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28281766 | ||||||
| chr13:28281810 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2384+431C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281810 | |||||||
| chr13:28281820 | G | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+441G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281820 | |||||||
| chr13:28281918 | G | A | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+539G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281918 | |||||||
| chr13:28282012 | G | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0003g0008 others(1): Show |
4 | HG02083.hp1 NA18979.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2384+633G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282012 | |||||||
| chr13:28282056 | A | G | 1 | a0001c0001t0006g0014 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2384+677A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282056 | |||||||
| chr13:28282068 | G | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+689G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282068 | |||||||
| chr13:28282233 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+854A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282233 | |||||||
| chr13:28282339 | T | TG | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+961dupG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282339 | ||||||
| chr13:28282340 | G | GT | 118 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0090 others(115): Show |
118 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.2384+973dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282340 | ||||||
| chr13:28282340 | G | GTT | 8 | a0001c0001t0003g0231 a0001c0001t0010g0121 a0001c0001t0010g0122 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+972_2384+973d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282340 | ||||||
| chr13:28282356 | A | G | 73 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(70): Show |
73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.2384+977A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282356 | |||||||
| chr13:28282409 | C | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+1030C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282409 | |||||||
| chr13:28282777 | C | T | 14 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.2384+1398C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282777 | |||||||
| chr13:28282880 | G | GTTTA | 88 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(85): Show |
88 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.2384+1525_2384+152 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282880 | ||||||
| chr13:28282880 | G | GTTTATTT others(1): Show |
6 | a0001c0001t0001g0096 a0001c0001t0001g0134 a0001c0001t0001g0157 others(3): Show |
6 | HG00438.hp1 NA18941.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.2384+1521_2384+152 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282880 | ||||||
| chr13:28282920 | G | A | 12 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(9): Show |
12 | HG02080.hp1 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.2384+1541G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282920 | |||||||
| chr13:28282942 | A | G | 15 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(12): Show |
15 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2384+1563A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282942 | |||||||
| chr13:28283030 | C | G | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2384+1651C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283030 | |||||||
| chr13:28283073 | G | A | 84 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(81): Show |
84 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.2384+1694G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283073 | |||||||
| chr13:28283085 | A | G | 102 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(99): Show |
102 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(99): Show |
intron_variant | MODIFIER | c.2384+1706A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283085 | |||||||
| chr13:28283105 | A | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+1726A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283105 | |||||||
| chr13:28283127 | C | T | 15 | a0001c0001t0005g0117 a0001c0001t0005g0176 a0001c0001t0005g0179 others(12): Show |
15 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2384+1748C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283127 | |||||||
| chr13:28283241 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2384+1862G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283241 | |||||||
| chr13:28283306 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+1927T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283306 | |||||||
| chr13:28283326 | G | A | 2 | a0001c0001t0017g0204 a0001c0001t0017g0205 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2384+1947G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283326 | |||||||
| chr13:28283378 | T | A | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384+1999T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283378 | |||||||
| chr13:28283450 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2384+2071A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283450 | |||||||
| chr13:28283468 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2384+2089A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283468 | |||||||
| chr13:28283552 | A | T | 94 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(91): Show |
94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.2384+2173A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283552 | |||||||
| chr13:28283571 | A | G | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+2192A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283571 | |||||||
| chr13:28283629 | C | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2384+2250C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283629 | |||||||
| chr13:28283641 | A | G | 9 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.2384+2262A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283641 | |||||||
| chr13:28283737 | T | C | 11 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(8): Show |
11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2384+2358T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283737 | |||||||
| chr13:28283796 | G | A | 8 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(5): Show |
8 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2384+2417G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283796 | |||||||
| chr13:28284061 | G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2384+2682G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284061 | |||||||
| chr13:28284155 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2384+2776T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284155 | |||||||
| chr13:28284381 | A | AT | 19 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0054 others(16): Show |
19 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2384+3018dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28284381 | ||||||
| chr13:28284381 | AT | A | 13 | a0001c0001t0001g0058 a0001c0001t0011g0187 a0001c0001t0011g0242 others(10): Show |
13 | HG01109.hp1 HG02572.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.2384+3018delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28284381 | ||||||
| chr13:28284531 | G | T | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+3152G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284531 | |||||||
| chr13:28284664 | T | A | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2384+3285T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284664 | |||||||
| chr13:28284675 | C | T | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+3296C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284675 | |||||||
| chr13:28284877 | A | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2385-3107A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284877 | |||||||
| chr13:28285434 | T | C | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2385-2550T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28285434 | |||||||
| chr13:28285662 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2385-2322A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28285662 | |||||||
| chr13:28286237 | A | G | 1 | a0001c0001t0005g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2385-1747A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28286237 | |||||||
| chr13:28286601 | G | A | 2 | a0001c0001t0005g0182 a0001c0001t0007g0180 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2385-1383G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28286601 | |||||||
| chr13:28286778 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2385-1206A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28286778 | |||||||
| chr13:28287004 | C | T | 70 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(67): Show |
70 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.2385-980C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287004 | |||||||
| chr13:28287054 | G | A | 9 | a0001c0001t0001g0054 a0001c0001t0004g0100 a0001c0001t0010g0121 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.2385-930G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287054 | |||||||
| chr13:28287127 | A | G | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2385-857A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287127 | |||||||
| chr13:28287253 | T | C | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2385-731T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287253 | |||||||
| chr13:28287369 | G | A | 32 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(29): Show |
32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2385-615G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287369 | |||||||
| chr13:28287478 | C | T | 1 | a0001c0001t0042g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2385-506C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287478 | |||||||
| chr13:28287533 | A | G | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2385-451A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287533 | |||||||
| chr13:28287565 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2385-419C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287565 | |||||||
| chr13:28287698 | T | C | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.2385-286T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287698 | |||||||
| chr13:28287929 | A | G | 96 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(93): Show |
96 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.2385-55A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287929 | |||||||
| chr13:28288492 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2523+370A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288492 | |||||||
| chr13:28288665 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2523+543C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288665 | |||||||
| chr13:28288752 | T | A | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0175 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2523+630T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288752 | |||||||
| chr13:28288828 | A | AT | 102 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(99): Show |
102 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.2523+726dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288828 | ||||||
| chr13:28288828 | A | ATT | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
9 | HG01167.hp2 HG02071.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.2523+725_2523+726d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288828 | ||||||
| chr13:28288858 | T | TCTCA | 141 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.2523+739_2523+740i others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288858 | ||||||
| chr13:28288858 | T | TCTCG | 94 | a0001c0001t0001g0213 a0001c0001t0002g0002 a0001c0001t0002g0011 others(91): Show |
94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.2523+739_2523+740i others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288858 | ||||||
| chr13:28288879 | T | C | 14 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2523+757T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288879 | |||||||
| chr13:28288895 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2523+773A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288895 | |||||||
| chr13:28288902 | C | T | 1 | a0001c0001t0007g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2523+780C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288902 | |||||||
| chr13:28288919 | C | T | 21 | a0001c0001t0005g0117 a0001c0001t0005g0172 a0001c0001t0005g0173 others(18): Show |
21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2523+797C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288919 | |||||||
| chr13:28289007 | T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2523+885T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289007 | |||||||
| chr13:28289061 | C | T | 45 | a0001c0001t0002g0012 a0001c0001t0002g0036 a0001c0001t0002g0037 others(42): Show |
45 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2523+939C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289061 | |||||||
| chr13:28289106 | A | G | 2 | a0001c0001t0032g0227 a0001c0001t0043g0252 |
2 | HG02602.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2523+984A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289106 | |||||||
| chr13:28289178 | A | G | 8 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG02080.hp2 HG02523.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.2523+1056A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289178 | |||||||
| chr13:28289200 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2523+1078G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289200 | |||||||
| chr13:28289467 | G | A | 6 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0188 others(3): Show |
6 | HG00639.hp2 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2523+1345G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289467 | |||||||
| chr13:28289610 | A | G | 8 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0003g0229 others(5): Show |
8 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2523+1488A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289610 | |||||||
| chr13:28289613 | A | G | 9 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0003g0229 others(6): Show |
9 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2523+1491A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289613 | |||||||
| chr13:28289618 | G | A | 8 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0003g0229 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2523+1496G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289618 | |||||||
| chr13:28289632 | A | T | 5 | a0001c0001t0008g0244 a0001c0001t0008g0245 a0001c0001t0008g0246 others(2): Show |
5 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+1510A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289632 | |||||||
| chr13:28289638 | T | G | 2 | a0001c0001t0011g0184 a0001c0001t0019g0185 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2523+1516T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289638 | |||||||
| chr13:28289648 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2523+1526A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289648 | |||||||
| chr13:28289649 | C | A | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2523+1527C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289649 | |||||||
| chr13:28289653 | G | A | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2523+1531G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289653 | |||||||
| chr13:28289698 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2523+1576G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289698 | |||||||
| chr13:28289739 | G | A | 7 | a0001c0001t0003g0010 a0001c0001t0010g0121 a0001c0001t0010g0122 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2523+1617G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289739 | |||||||
| chr13:28289879 | C | G | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2523+1757C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289879 | |||||||
| chr13:28289897 | A | G | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2523+1775A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289897 | |||||||
| chr13:28290063 | C | T | 5 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+1941C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290063 | |||||||
| chr13:28290095 | G | A | 1 | a0001c0001t0032g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2523+1973G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290095 | |||||||
| chr13:28290112 | A | G | 1 | a0001c0001t0009g0217 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2523+1990A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290112 | |||||||
| chr13:28290235 | A | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0244 a0001c0001t0008g0245 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2523+2113A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290235 | |||||||
| chr13:28290405 | G | C | 1 | a0001c0001t0007g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2524-1977G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290405 | |||||||
| chr13:28290414 | T | C | 2 | a0001c0001t0013g0016 a0001c0001t0046g0035 |
2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2524-1968T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290414 | |||||||
| chr13:28290485 | C | T | 7 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2524-1897C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290485 | |||||||
| chr13:28290511 | A | G | 128 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0012 others(125): Show |
128 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.2524-1871A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290511 | |||||||
| chr13:28290614 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0169 |
2 | NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2524-1768A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290614 | |||||||
| chr13:28290713 | A | G | 1 | a0001c0001t0047g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2524-1669A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290713 | |||||||
| chr13:28290955 | T | TATTC | 246 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.2524-1424_2524-142 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28290955 | ||||||
| chr13:28291059 | A | G | 1 | a0001c0001t0004g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2524-1323A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291059 | |||||||
| chr13:28291205 | ATGTT | A | 3 | a0001c0001t0001g0075 a0001c0001t0004g0068 a0001c0008t0001g0069 |
3 | HG01358.hp1 HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2524-1174_2524-117 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28291205 | ||||||
| chr13:28291260 | A | G | 80 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0012 others(77): Show |
80 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.2524-1122A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291260 | |||||||
| chr13:28291723 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0035g0200 |
2 | NA18974.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2524-659C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291723 | |||||||
| chr13:28291724 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2524-658G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291724 | |||||||
| chr13:28291790 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0012 others(66): Show |
69 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.2524-592C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291790 | |||||||
| chr13:28291858 | T | A | 2 | a0001c0001t0013g0127 a0001c0001t0013g0128 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2524-524T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291858 | |||||||
| chr13:28291987 | T | C | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0052 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2524-395T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291987 | |||||||
| chr13:28292080 | C | A | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2524-302C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292080 | |||||||
| chr13:28292127 | G | T | 247 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.2524-255G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292127 | |||||||
| chr13:28292159 | A | G | 142 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.2524-223A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292159 | |||||||
| chr13:28292207 | A | C | 1 | a0001c0001t0024g0228 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2524-175A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292207 | |||||||
| chr13:28292283 | CA | C | 10 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(7): Show |
10 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2524-91delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28292283 | ||||||
| chr13:28292310 | T | C | 3 | a0001c0001t0015g0250 a0001c0001t0029g0249 a0003c0006t0015g0251 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2524-72T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292310 | |||||||
| chr13:28292323 | GTAGA | G | 8 | a0001c0001t0010g0121 a0001c0001t0010g0122 a0001c0001t0010g0124 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2524-56_2524-53del others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28292323 |