Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1362 |
| ensemblid | ENSG00000108582.12 |
| hgncid | 2301 |
| symbol | CPD |
| name | carboxypeptidase D |
| refseq_nuc | NM_001304.5 |
| refseq_prot | NP_001295.2 |
| ensembl_nuc | ENST00000225719.9 |
| ensembl_prot | ENSP00000225719.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 30378927 |
| end | 30469989 |
| strand | + |
| ver | v1.2 |
| region | chr17:30378927-30469989 |
| region5000 | chr17:30373927-30474989 |
| regionname0 | CPD_chr17_30378927_30469989 |
| regionname5000 | CPD_chr17_30373927_30474989 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1380 | 279 | 75 | 61 | 92 | 12 | 37 | 70 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0002 | 0/0 | 1380 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0003 | 0/0 | 1380 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0004 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0005 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0006 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0007 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0008 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0009 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | MASGL others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0010 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| a0011 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | MASGR others(1375): Show |
chr17 | 30373927 | 30474989 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4140 | 262 | 73 | 57 | 83 | 12 | 35 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0001c0003 | 0/0 | 4140 | 5 | 0 | 0 | 5 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0001c0004 | 0/0 | 4140 | 5 | 0 | 0 | 4 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0001c0005 | 0/0 | 4140 | 3 | 0 | 3 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0001c0006 | 0/0 | 4140 | 2 | 2 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0001c0008 | 0/0 | 4140 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0001c0009 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0002c0002 | 0/0 | 4140 | 7 | 6 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0003c0016 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0003c0017 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0004c0007 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0005c0013 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0006c0014 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0007c0010 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0008c0015 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0009c0018 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0010c0012 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 | ||
| a0011c0011 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | ATGGC others(4135): Show |
chr17 | 30373927 | 30474989 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9372 | 102 | 22 | 21 | 37 | 3 | 19 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0002 | 1/1 | 9372 | 90 | 12 | 25 | 31 | 5 | 15 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0003 | 0/0 | 9372 | 13 | 12 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0004 | 0/0 | 9368 | 10 | 0 | 1 | 8 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9363): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0005 | 0/0 | 9366 | 9 | 6 | 2 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9361): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0006 | 0/0 | 9372 | 5 | 5 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0007 | 0/0 | 9370 | 4 | 4 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9365): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0008 | 0/0 | 9366 | 3 | 3 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9361): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0009 | 0/0 | 9372 | 4 | 3 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0010 | 0/0 | 9372 | 3 | 0 | 1 | 0 | 2 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0011 | 0/0 | 9372 | 3 | 0 | 3 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0012 | 0/0 | 9372 | 2 | 0 | 0 | 2 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0013 | 0/0 | 9372 | 2 | 2 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0014 | 0/0 | 9366 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9361): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0015 | 0/0 | 9366 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9361): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0017 | 0/0 | 9372 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0018 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0019 | 0/0 | 9372 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0020 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0021 | 0/0 | 9372 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0022 | 0/0 | 9372 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0023 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0024 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0025 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0001t0027 | 0/0 | 9372 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0003t0001 | 0/0 | 9372 | 5 | 0 | 0 | 5 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0004t0002 | 0/0 | 9372 | 5 | 0 | 0 | 4 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0005t0001 | 0/0 | 9372 | 3 | 0 | 3 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0006t0002 | 0/0 | 9372 | 2 | 2 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0008t0002 | 0/0 | 9372 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0001c0009t0001 | 0/0 | 9372 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0002c0002t0001 | 0/0 | 9372 | 6 | 6 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0002c0002t0026 | 0/0 | 9372 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0003c0016t0001 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0003c0017t0016 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9363): Show |
chr17 | 30373927 | 30474989 |
| a0004c0007t0001 | 0/0 | 9372 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0005c0013t0002 | 0/0 | 9372 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0006c0014t0002 | 0/0 | 9372 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0007c0010t0001 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0008c0015t0002 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0009c0018t0002 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0010c0012t0001 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9367): Show |
chr17 | 30373927 | 30474989 |
| a0011c0011t0008 | 0/0 | 9366 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | GCCCG others(9361): Show |
chr17 | 30373927 | 30474989 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0008g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0010g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0011g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0012g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0012g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0013g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0013g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0015g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0018g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0019g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0020g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0021g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0022g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0023g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0024g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0025g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0001t0027g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0005t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0005t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0006t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0006t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0008t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0001c0009t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0002c0002t0026g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0003c0016t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0003c0017t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0004c0007t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0005c0013t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0006c0014t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0007c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0008c0015t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0009c0018t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0010c0012t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| a0011c0011t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0154 | EUR | GBR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0199 | EUR | GBR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0037 | EUR | GBR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | FIN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00438 | hp1 | a0001 | c0001 | t0025 | g0044 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00544 | hp1 | a0001 | c0001 | t0020 | g0191 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00597 | hp1 | a0001 | c0004 | t0002 | g0224 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00639 | hp2 | a0001 | c0008 | t0002 | g0227 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00738 | hp2 | a0001 | c0001 | t0015 | g0271 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0120 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01169 | hp1 | a0001 | c0005 | t0001 | g0008 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0008 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0023 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0158 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0266 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0087 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01346 | hp1 | a0002 | c0002 | t0026 | g0030 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0103 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0265 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0156 | EUR | IBS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0264 | EUR | IBS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01517 | hp1 | a0001 | c0001 | t0010 | g0157 | EUR | IBS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01891 | hp2 | a0001 | c0001 | t0022 | g0131 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01981 | hp2 | a0001 | c0001 | t0019 | g0246 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0024 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02293 | hp2 | a0001 | c0005 | t0001 | g0007 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02683 | hp1 | a0001 | c0004 | t0002 | g0201 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02717 | hp2 | a0001 | c0001 | t0027 | g0027 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02735 | hp2 | a0001 | c0009 | t0001 | g0108 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02886 | hp2 | a0001 | c0006 | t0002 | g0025 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0132 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02970 | hp2 | a0001 | c0006 | t0002 | g0202 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02976 | hp2 | a0004 | c0007 | t0001 | g0125 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | GWD | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0017 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | ESN | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0275 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03453 | hp1 | a0005 | c0013 | t0002 | g0210 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0133 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03491 | hp2 | a0001 | c0001 | t0017 | g0196 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | STU | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03710 | hp2 | a0006 | c0014 | t0002 | g0209 | SAS | PJL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | STU | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | STU | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | YRI | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | CHB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | CHB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | YRI | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18946 | hp1 | a0001 | c0004 | t0002 | g0260 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18951 | hp1 | a0007 | c0010 | t0001 | g0002 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0228 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18962 | hp1 | a0001 | c0001 | t0012 | g0237 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18965 | hp2 | a0009 | c0018 | t0002 | g0239 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19000 | hp2 | a0001 | c0001 | t0024 | g0112 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19001 | hp1 | a0003 | c0017 | t0016 | g0051 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19001 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19010 | hp1 | a0001 | c0001 | t0018 | g0247 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19011 | hp2 | a0010 | c0012 | t0001 | g0077 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | LWK | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19055 | hp2 | a0003 | c0016 | t0001 | g0053 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19068 | hp1 | a0001 | c0004 | t0002 | g0198 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19087 | hp1 | a0001 | c0001 | t0023 | g0085 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19087 | hp2 | a0001 | c0001 | t0012 | g0208 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | YRI | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ASW | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ASW | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | GIH | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0128 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0272 | AFR | MSL | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA18955 | hp2 | a0008 | c0015 | t0002 | g0218 | EAS | JPT | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | USA | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA20300 | hp2 | a0001 | c0001 | t0021 | g0137 | AFR | USA | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | LWK | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| NA21309 | hp2 | a0011 | c0011 | t0008 | g0018 | AFR | LWK | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0212 | REF | REF | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0226 | REF | REF | CPD_chr17_30373927_30474989 | CPD | chr17 | 30373927 | 30474989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30378994 | G | T | 1 | a0009 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.14G>T | p.Arg5Leu | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 68/9372 | 14/4143 | 5/1380 | chr17 | 30378994 | |||
| chr17:30379096 | C | T | 1 | a0003 | 2 | NA19001.hp1 NA19055.hp2 |
missense_variant | MODERATE | c.116C>T | p.Ala39Val | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 170/9372 | 116/4143 | 39/1380 | chr17 | 30379096 | |||
| chr17:30379410 | G | T | 1 | a0008 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.430G>T | p.Val144Leu | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 484/9372 | 430/4143 | 144/1380 | chr17 | 30379410 | |||
| chr17:30379441 | G | A | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.461G>A | p.Arg154His | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 515/9372 | 461/4143 | 154/1380 | chr17 | 30379441 | |||
| chr17:30385152 | A | G | 1 | a0005 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.910A>G | p.Thr304Ala | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/21 | 964/9372 | 910/4143 | 304/1380 | chr17 | 30385152 | |||
| chr17:30420919 | C | T | 1 | a0006 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1073C>T | p.Pro358Leu | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 3/21 | 1127/9372 | 1073/4143 | 358/1380 | chr17 | 30420919 | |||
| chr17:30422775 | C | G | 1 | a0010 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1409C>G | p.Thr470Arg | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 5/21 | 1463/9372 | 1409/4143 | 470/1380 | chr17 | 30422775 | |||
| chr17:30422862 | A | G | 1 | a0002 | 7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
missense_variant | MODERATE | c.1496A>G | p.Lys499Arg | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 5/21 | 1550/9372 | 1496/4143 | 499/1380 | chr17 | 30422862 | |||
| chr17:30449581 | A | G | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2902A>G | p.Ile968Val | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/21 | 2956/9372 | 2902/4143 | 968/1380 | chr17 | 30449581 | |||
| chr17:30462007 | C | T | 1 | a0007 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.3761C>T | p.Pro1254Leu | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 19/21 | 3815/9372 | 3761/4143 | 1254/1380 | chr17 | 30462007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30378993 | C | A | 1 | a0001c0006 | 2 | HG02886.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.13C>A | p.Arg5Arg | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 67/9372 | 13/4143 | 5/1380 | chr17 | 30378993 | |||
| chr17:30379325 | C | T | 1 | a0001c0005 | 3 | HG01169.hp1 HG01192.hp1 HG02293.hp2 |
synonymous_variant | LOW | c.345C>T | p.Asp115Asp | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 399/9372 | 345/4143 | 115/1380 | chr17 | 30379325 | |||
| chr17:30385019 | C | T | 3 | a0001c0004 a0006c0014 a0008c0015 |
7 | HG00597.hp1 HG02683.hp1 HG03710.hp2 others(4): Show |
synonymous_variant | LOW | c.777C>T | p.Gly259Gly | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/21 | 831/9372 | 777/4143 | 259/1380 | chr17 | 30385019 | |||
| chr17:30422746 | G | A | 1 | a0001c0008 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1380G>A | p.Arg460Arg | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 5/21 | 1434/9372 | 1380/4143 | 460/1380 | chr17 | 30422746 | |||
| chr17:30461284 | G | A | 1 | a0001c0009 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.3603G>A | p.Lys1201Lys | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/21 | 3657/9372 | 3603/4143 | 1201/1380 | chr17 | 30461284 | |||
| chr17:30464601 | G | A | 2 | a0001c0003 a0003c0016 |
6 | HG00544.hp2 HG00597.hp2 NA18612.hp1 others(3): Show |
synonymous_variant | LOW | c.3930G>A | p.Ser1310Ser | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 3984/9372 | 3930/4143 | 1310/1380 | chr17 | 30464601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30378951 | C | T | 1 | a0001c0001t0027 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/21 | 30 | chr17 | 30378951 | ||||||
| chr17:30464859 | T | C | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*45T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 45 | chr17 | 30464859 | ||||||
| chr17:30465048 | ACTTTTT | A | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0014 others(2): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*241_*246delCTTTTT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 241 | INFO_REALIGN_3_PRIME | chr17 | 30465048 | |||||
| chr17:30465131 | A | C | 1 | a0002c0002t0026 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*317A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 317 | chr17 | 30465131 | ||||||
| chr17:30465426 | C | A | 1 | a0001c0001t0010 | 3 | HG01243.hp1 HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*612C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 612 | chr17 | 30465426 | ||||||
| chr17:30466299 | T | C | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0014 others(2): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1485T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 1485 | chr17 | 30466299 | ||||||
| chr17:30466339 | C | A | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1525C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 1525 | chr17 | 30466339 | ||||||
| chr17:30466555 | ATAGT | A | 2 | a0001c0001t0004 a0003c0017t0016 |
11 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1746_*1749delTAGT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 1746 | INFO_REALIGN_3_PRIME | chr17 | 30466555 | |||||
| chr17:30466612 | A | G | 1 | a0001c0001t0011 | 3 | HG01109.hp2 HG01261.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1798A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 1798 | chr17 | 30466612 | ||||||
| chr17:30466797 | G | A | 1 | a0001c0001t0017 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1983G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 1983 | chr17 | 30466797 | ||||||
| chr17:30467002 | A | G | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(26): Show |
185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*2188A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2188 | chr17 | 30467002 | ||||||
| chr17:30467195 | C | T | 1 | a0001c0001t0006 | 5 | HG02145.hp2 HG02486.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2381C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2381 | chr17 | 30467195 | ||||||
| chr17:30467259 | C | T | 1 | a0001c0001t0025 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2445C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2445 | chr17 | 30467259 | ||||||
| chr17:30467357 | T | A | 1 | a0001c0001t0012 | 2 | NA18962.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2543T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2543 | chr17 | 30467357 | ||||||
| chr17:30467393 | T | C | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2579T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2579 | chr17 | 30467393 | ||||||
| chr17:30467502 | G | T | 1 | a0003c0017t0016 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2688G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2688 | chr17 | 30467502 | ||||||
| chr17:30467530 | G | C | 1 | a0001c0001t0021 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2716G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2716 | chr17 | 30467530 | ||||||
| chr17:30467718 | A | G | 1 | a0001c0001t0003 | 13 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2904A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2904 | chr17 | 30467718 | ||||||
| chr17:30467725 | G | A | 1 | a0001c0001t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2911G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 2911 | chr17 | 30467725 | ||||||
| chr17:30468339 | A | G | 1 | a0001c0001t0015 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3525A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 3525 | chr17 | 30468339 | ||||||
| chr17:30468408 | CAG | C | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3595_*3596delAG | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 3595 | chr17 | 30468408 | ||||||
| chr17:30468411 | T | G | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3597T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 3597 | chr17 | 30468411 | ||||||
| chr17:30468677 | C | T | 3 | a0001c0001t0008 a0001c0001t0014 a0011c0011t0008 |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3863C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 3863 | chr17 | 30468677 | ||||||
| chr17:30468734 | G | A | 2 | a0001c0001t0004 a0003c0017t0016 |
11 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3920G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 3920 | chr17 | 30468734 | ||||||
| chr17:30468871 | T | C | 1 | a0001c0001t0023 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4057T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4057 | chr17 | 30468871 | ||||||
| chr17:30469167 | A | T | 1 | a0001c0001t0020 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4353A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4353 | chr17 | 30469167 | ||||||
| chr17:30469177 | T | A | 1 | a0001c0001t0014 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4363T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4363 | chr17 | 30469177 | ||||||
| chr17:30469186 | A | G | 1 | a0001c0001t0009 | 4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4372A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4372 | chr17 | 30469186 | ||||||
| chr17:30469339 | C | T | 1 | a0001c0001t0019 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4525C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4525 | chr17 | 30469339 | ||||||
| chr17:30469588 | G | A | 1 | a0001c0001t0013 | 2 | HG02896.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4774G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4774 | chr17 | 30469588 | ||||||
| chr17:30469647 | G | T | 1 | a0001c0001t0018 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4833G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 4833 | chr17 | 30469647 | ||||||
| chr17:30469920 | T | C | 1 | a0001c0001t0024 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5106T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 21/21 | 5106 | chr17 | 30469920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30379796 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+70A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30379796 | |||||||
| chr17:30379917 | T | C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+191T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30379917 | |||||||
| chr17:30379979 | G | T | 14 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(11): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.746+253G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30379979 | |||||||
| chr17:30379985 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.746+259A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30379985 | |||||||
| chr17:30380218 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.746+492T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30380218 | |||||||
| chr17:30380223 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.746+497T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30380223 | |||||||
| chr17:30380499 | G | A | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+773G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30380499 | |||||||
| chr17:30380501 | G | T | 1 | a0001c0004t0002g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.746+775G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30380501 | |||||||
| chr17:30380985 | T | C | 1 | a0001c0006t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.746+1259T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30380985 | |||||||
| chr17:30380993 | A | ATTTCTTC others(3): Show |
1 | a0001c0001t0001g0259 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.746+1268_746+1277d others(12): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | 30380993 | ||||||
| chr17:30381047 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.746+1321T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381047 | |||||||
| chr17:30381097 | TTGATAAG others(25): Show |
T | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1372_746+1403d others(34): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381097 | |||||||
| chr17:30381138 | T | C | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.746+1412T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381138 | |||||||
| chr17:30381225 | T | A | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1499T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381225 | |||||||
| chr17:30381285 | T | A | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1559T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381285 | |||||||
| chr17:30381424 | T | G | 1 | a0001c0001t0027g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.746+1698T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381424 | |||||||
| chr17:30381544 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1818A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381544 | |||||||
| chr17:30381582 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1856A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381582 | |||||||
| chr17:30381671 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1945A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381671 | |||||||
| chr17:30381703 | T | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+1977T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381703 | |||||||
| chr17:30381703 | T | TGGAATAT others(20): Show |
1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+1977_746+1978i others(29): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381703 | |||||||
| chr17:30381806 | A | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.746+2080A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381806 | |||||||
| chr17:30381845 | G | GTTA | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.746+2122_746+2124d others(5): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | 30381845 | ||||||
| chr17:30381853 | G | A | 11 | a0001c0001t0001g0036 a0001c0001t0004g0035 a0001c0001t0004g0037 others(8): Show |
11 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.746+2127G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381853 | |||||||
| chr17:30381971 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.746+2245A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30381971 | |||||||
| chr17:30382037 | G | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.746+2311G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382037 | |||||||
| chr17:30382277 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.746+2551A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382277 | |||||||
| chr17:30382408 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.747-2581C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382408 | |||||||
| chr17:30382598 | T | A | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-2391T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382598 | |||||||
| chr17:30382868 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.747-2121G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382868 | |||||||
| chr17:30382945 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.747-2044T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382945 | |||||||
| chr17:30382946 | G | T | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.747-2043G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382946 | |||||||
| chr17:30382947 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.747-2042T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30382947 | |||||||
| chr17:30383005 | A | C | 11 | a0001c0001t0002g0001 a0001c0001t0002g0238 a0001c0001t0002g0240 others(8): Show |
15 | HG01978.hp2 HG01981.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.747-1984A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383005 | |||||||
| chr17:30383280 | C | T | 1 | a0001c0001t0009g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.747-1709C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383280 | |||||||
| chr17:30383316 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.747-1673T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383316 | |||||||
| chr17:30383382 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-1607C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383382 | |||||||
| chr17:30383393 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.747-1596G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383393 | |||||||
| chr17:30383606 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.747-1383T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383606 | |||||||
| chr17:30383740 | T | A | 1 | a0001c0001t0001g0026 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.747-1249T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383740 | |||||||
| chr17:30383790 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.747-1199A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383790 | |||||||
| chr17:30383862 | T | C | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.747-1127T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383862 | |||||||
| chr17:30383978 | G | A | 1 | a0001c0001t0005g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.747-1011G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383978 | |||||||
| chr17:30383983 | T | G | 1 | a0001c0001t0002g0012 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.747-1006T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30383983 | |||||||
| chr17:30384030 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.747-959T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30384030 | |||||||
| chr17:30384388 | A | T | 1 | a0001c0001t0012g0237 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.747-601A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30384388 | |||||||
| chr17:30384392 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.747-597A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30384392 | |||||||
| chr17:30384578 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.747-411C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30384578 | |||||||
| chr17:30384936 | A | T | 1 | a0001c0001t0007g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.747-53A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 1/20 | chr17 | 30384936 | |||||||
| chr17:30385345 | TATTTATT others(231): Show |
T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0047 |
3 | HG03710.hp1 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.994+111_994+348del | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30385345 | ||||||
| chr17:30385393 | C | T | 10 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(7): Show |
11 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.994+157C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30385393 | |||||||
| chr17:30385504 | G | GCA | 3 | a0001c0001t0002g0236 a0001c0001t0012g0237 a0001c0001t0020g0191 |
3 | HG00544.hp1 HG01261.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.994+295_994+296dup others(2): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30385504 | ||||||
| chr17:30385504 | GCA | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0076 a0001c0001t0001g0080 others(6): Show |
9 | HG00099.hp1 HG00323.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+295_994+296del others(2): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30385504 | ||||||
| chr17:30385504 | GCACA | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(112): Show |
121 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.994+293_994+296del others(4): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30385504 | ||||||
| chr17:30385504 | GCACACA | G | 52 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0036 others(49): Show |
54 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.994+291_994+296del others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30385504 | ||||||
| chr17:30385533 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.994+297A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30385533 | |||||||
| chr17:30386107 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.994+871G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30386107 | |||||||
| chr17:30386237 | G | A | 3 | a0001c0001t0010g0156 a0001c0001t0010g0157 a0001c0001t0010g0158 |
3 | HG01243.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.994+1001G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30386237 | |||||||
| chr17:30386688 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+1452A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30386688 | |||||||
| chr17:30386708 | T | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.994+1472T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30386708 | |||||||
| chr17:30386771 | T | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.994+1535T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30386771 | |||||||
| chr17:30386995 | G | A | 1 | a0001c0006t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.994+1759G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30386995 | |||||||
| chr17:30387208 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.994+1972C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30387208 | |||||||
| chr17:30387225 | C | T | 3 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG03490.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.994+1989C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30387225 | |||||||
| chr17:30387365 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.994+2129T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30387365 | |||||||
| chr17:30387407 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+2171G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30387407 | |||||||
| chr17:30387782 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.994+2546T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30387782 | |||||||
| chr17:30387793 | C | T | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.994+2557C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30387793 | |||||||
| chr17:30388058 | C | T | 1 | a0001c0003t0001g0138 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.994+2822C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388058 | |||||||
| chr17:30388175 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
106 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.994+2939G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388175 | |||||||
| chr17:30388202 | G | A | 1 | a0001c0001t0005g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.994+2966G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388202 | |||||||
| chr17:30388467 | C | T | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.994+3231C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388467 | |||||||
| chr17:30388536 | A | G | 1 | a0001c0001t0011g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.994+3300A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388536 | |||||||
| chr17:30388649 | C | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(8): Show |
12 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.994+3413C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388649 | |||||||
| chr17:30388660 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.994+3424C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388660 | |||||||
| chr17:30388777 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(8): Show |
12 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.994+3541C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388777 | |||||||
| chr17:30388876 | G | A | 1 | a0001c0001t0005g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.994+3640G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388876 | |||||||
| chr17:30388963 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+3727A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388963 | |||||||
| chr17:30388966 | G | C | 16 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(13): Show |
17 | HG00544.hp2 HG00597.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.994+3730G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30388966 | |||||||
| chr17:30389098 | G | A | 2 | a0001c0001t0006g0121 a0001c0001t0006g0122 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.994+3862G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389098 | |||||||
| chr17:30389635 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.994+4399A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389635 | |||||||
| chr17:30389662 | C | A | 1 | a0001c0001t0002g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.994+4426C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389662 | |||||||
| chr17:30389671 | G | C | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.994+4435G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389671 | |||||||
| chr17:30389737 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.994+4501A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389737 | |||||||
| chr17:30389756 | C | G | 1 | a0002c0002t0001g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.994+4520C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389756 | |||||||
| chr17:30389757 | T | A | 1 | a0002c0002t0001g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.994+4521T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389757 | |||||||
| chr17:30389917 | T | C | 1 | a0002c0002t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.994+4681T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389917 | |||||||
| chr17:30389935 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.994+4699G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30389935 | |||||||
| chr17:30390316 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.994+5080G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390316 | |||||||
| chr17:30390318 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.994+5082G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390318 | |||||||
| chr17:30390491 | T | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0016 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.994+5255T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390491 | |||||||
| chr17:30390499 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.994+5263G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390499 | |||||||
| chr17:30390627 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.994+5391C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390627 | |||||||
| chr17:30390631 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.994+5395G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390631 | |||||||
| chr17:30390700 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.994+5464T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390700 | |||||||
| chr17:30390860 | G | A | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 |
3 | HG01192.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.994+5624G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390860 | |||||||
| chr17:30390990 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.994+5754C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30390990 | |||||||
| chr17:30391064 | A | G | 1 | a0001c0004t0002g0228 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.994+5828A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30391064 | |||||||
| chr17:30391120 | G | A | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+5884G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30391120 | |||||||
| chr17:30391132 | CT | C | 120 | a0001c0001t0001g0020 a0001c0001t0001g0057 a0001c0001t0001g0117 others(117): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.994+5917delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30391132 | ||||||
| chr17:30391132 | CTT | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.994+5916_994+5917d others(4): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30391132 | ||||||
| chr17:30391132 | CTTT | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
7 | HG01069.hp2 HG01074.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.994+5915_994+5917d others(5): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30391132 | ||||||
| chr17:30391188 | A | T | 1 | a0001c0001t0021g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.994+5952A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30391188 | |||||||
| chr17:30391190 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.994+5954C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30391190 | |||||||
| chr17:30391324 | G | A | 4 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(1): Show |
4 | HG00735.hp1 HG01069.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+6088G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30391324 | |||||||
| chr17:30392008 | C | CT | 17 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0140 others(14): Show |
21 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.994+6790dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30392008 | ||||||
| chr17:30392058 | G | A | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+6822G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30392058 | |||||||
| chr17:30392077 | T | G | 1 | a0001c0001t0002g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.994+6841T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30392077 | |||||||
| chr17:30392225 | C | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.994+6989C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30392225 | |||||||
| chr17:30392230 | T | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.994+6994T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30392230 | |||||||
| chr17:30392309 | C | T | 1 | a0001c0004t0002g0224 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.994+7073C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30392309 | |||||||
| chr17:30392574 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.994+7338A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30392574 | |||||||
| chr17:30393153 | A | G | 14 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(11): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.994+7917A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30393153 | |||||||
| chr17:30393379 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0060 others(2): Show |
7 | HG00438.hp2 HG02056.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.994+8143C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30393379 | |||||||
| chr17:30393442 | C | T | 5 | a0001c0001t0005g0263 a0001c0001t0005g0267 a0001c0001t0005g0268 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+8206C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30393442 | |||||||
| chr17:30393723 | A | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.994+8487A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30393723 | |||||||
| chr17:30394102 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.994+8866C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30394102 | |||||||
| chr17:30394116 | C | CT | 25 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0002g0001 others(22): Show |
29 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.994+8909dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394116 | ||||||
| chr17:30394116 | CT | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(108): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.994+8909delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394116 | ||||||
| chr17:30394116 | CTT | C | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
18 | HG00738.hp2 HG01069.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.994+8908_994+8909d others(4): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394116 | ||||||
| chr17:30394116 | CTTT | C | 7 | a0001c0001t0021g0137 a0002c0002t0001g0028 a0002c0002t0001g0029 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.994+8907_994+8909d others(5): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394116 | ||||||
| chr17:30394116 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+8900_994+8909d others(12): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394116 | ||||||
| chr17:30394176 | G | GA | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.994+8950dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394176 | ||||||
| chr17:30394305 | G | A | 2 | a0001c0001t0001g0124 a0004c0007t0001g0125 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.994+9069G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30394305 | |||||||
| chr17:30394408 | A | G | 2 | a0001c0001t0013g0132 a0001c0001t0013g0133 |
2 | HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.994+9172A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30394408 | |||||||
| chr17:30394483 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+9247T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30394483 | |||||||
| chr17:30394733 | G | A | 5 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(2): Show |
5 | NA18962.hp2 NA18986.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+9497G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30394733 | |||||||
| chr17:30394833 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.994+9597G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30394833 | |||||||
| chr17:30394901 | A | ATG | 8 | a0001c0001t0001g0140 a0001c0001t0002g0167 a0001c0001t0002g0168 others(5): Show |
8 | HG00438.hp2 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.994+9689_994+9690d others(4): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394901 | ||||||
| chr17:30394901 | A | ATGTG | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(129): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.994+9687_994+9690d others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394901 | ||||||
| chr17:30394901 | A | ATGTGTG | 7 | a0001c0001t0001g0065 a0001c0001t0001g0261 a0001c0001t0011g0103 others(4): Show |
7 | HG00738.hp2 HG01358.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.994+9685_994+9690d others(8): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394901 | ||||||
| chr17:30394901 | A | ATGTGTGT others(1): Show |
4 | a0001c0001t0006g0121 a0001c0001t0006g0122 a0001c0001t0006g0126 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+9683_994+9690d others(10): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30394901 | ||||||
| chr17:30395196 | C | CT | 18 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0140 others(15): Show |
19 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.994+9981dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30395196 | ||||||
| chr17:30395216 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.994+9980T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30395216 | |||||||
| chr17:30395235 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+9999A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30395235 | |||||||
| chr17:30395619 | G | T | 1 | a0004c0007t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.994+10383G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30395619 | |||||||
| chr17:30395689 | T | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+10453T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30395689 | |||||||
| chr17:30395720 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.994+10484C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30395720 | |||||||
| chr17:30395721 | A | AT | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.994+10488dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30395721 | ||||||
| chr17:30395724 | T | TA | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(135): Show |
145 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.994+10502dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30395724 | ||||||
| chr17:30396391 | A | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+11155A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30396391 | |||||||
| chr17:30396429 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.994+11193G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30396429 | |||||||
| chr17:30396506 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.994+11270A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30396506 | |||||||
| chr17:30396544 | GA | G | 5 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0145 others(2): Show |
5 | HG01433.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+11312delA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30396544 | ||||||
| chr17:30396601 | C | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(217): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.994+11365C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30396601 | |||||||
| chr17:30396822 | C | A | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.994+11586C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30396822 | |||||||
| chr17:30397499 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.994+12263G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30397499 | |||||||
| chr17:30397503 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.994+12267C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30397503 | |||||||
| chr17:30397612 | T | C | 4 | a0001c0001t0005g0267 a0001c0001t0005g0268 a0001c0001t0005g0269 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+12376T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30397612 | |||||||
| chr17:30397737 | C | CA | 44 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0062 others(41): Show |
45 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.994+12526dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30397737 | ||||||
| chr17:30397737 | CA | C | 19 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(16): Show |
19 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.994+12526delA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30397737 | ||||||
| chr17:30397920 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.994+12684G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30397920 | |||||||
| chr17:30397953 | G | A | 1 | a0001c0001t0022g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.994+12717G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30397953 | |||||||
| chr17:30398014 | C | CA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(23): Show |
29 | HG00673.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.994+12791dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30398014 | ||||||
| chr17:30398122 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.994+12886C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398122 | |||||||
| chr17:30398123 | G | A | 2 | a0001c0001t0013g0132 a0001c0001t0013g0133 |
2 | HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.994+12887G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398123 | |||||||
| chr17:30398233 | TAGAAC | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.994+13002_994+1300 others(9): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30398233 | ||||||
| chr17:30398235 | GAACAGAA others(6): Show |
G | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+13002_994+1301 others(17): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30398235 | ||||||
| chr17:30398238 | C | T | 26 | a0001c0001t0001g0140 a0001c0001t0003g0011 a0001c0001t0003g0142 others(23): Show |
28 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+13002C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398238 | |||||||
| chr17:30398264 | T | A | 25 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(22): Show |
27 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.994+13028T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398264 | |||||||
| chr17:30398285 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.994+13049C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398285 | |||||||
| chr17:30398570 | T | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.994+13334T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398570 | |||||||
| chr17:30398732 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.994+13496C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30398732 | |||||||
| chr17:30399342 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.994+14106T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30399342 | |||||||
| chr17:30399371 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.994+14135G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30399371 | |||||||
| chr17:30399521 | C | T | 1 | a0011c0011t0008g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+14285C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30399521 | |||||||
| chr17:30399561 | C | T | 2 | a0001c0001t0004g0042 a0001c0001t0004g0043 |
2 | HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.994+14325C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30399561 | |||||||
| chr17:30399650 | G | A | 10 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(7): Show |
11 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.994+14414G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30399650 | |||||||
| chr17:30399879 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.994+14643A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30399879 | |||||||
| chr17:30400150 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.994+14914C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400150 | |||||||
| chr17:30400171 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0079 a0001c0001t0001g0104 |
3 | HG02698.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.994+14935T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400171 | |||||||
| chr17:30400370 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0001g0129 others(5): Show |
9 | HG01175.hp1 HG01891.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+15134C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400370 | |||||||
| chr17:30400410 | A | G | 1 | a0006c0014t0002g0209 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.994+15174A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400410 | |||||||
| chr17:30400420 | A | T | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.994+15184A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400420 | |||||||
| chr17:30400425 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.994+15189T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400425 | |||||||
| chr17:30400652 | C | CT | 8 | a0001c0001t0002g0160 a0001c0001t0002g0168 a0001c0001t0002g0169 others(5): Show |
8 | HG01884.hp1 HG01981.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.994+15440dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400652 | ||||||
| chr17:30400652 | C | CTTT | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(106): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.994+15438_994+1544 others(7): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400652 | ||||||
| chr17:30400652 | C | CTTTT | 21 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0095 others(18): Show |
21 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.994+15437_994+1544 others(8): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400652 | ||||||
| chr17:30400652 | C | CTTTTT | 10 | a0001c0001t0001g0068 a0001c0001t0007g0272 a0001c0001t0007g0273 others(7): Show |
10 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.994+15436_994+1544 others(9): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400652 | ||||||
| chr17:30400652 | CT | C | 15 | a0001c0001t0002g0155 a0001c0001t0002g0162 a0001c0001t0002g0197 others(12): Show |
16 | HG00323.hp1 HG01074.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.994+15440delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400652 | ||||||
| chr17:30400812 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.994+15576C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400812 | |||||||
| chr17:30400819 | G | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.994+15583G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400819 | |||||||
| chr17:30400820 | G | A | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.994+15584G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400820 | |||||||
| chr17:30400824 | A | AT | 8 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0102 others(5): Show |
8 | HG03688.hp1 NA18994.hp2 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.994+15607dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400824 | ||||||
| chr17:30400824 | AT | A | 8 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(5): Show |
8 | HG01192.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.994+15607delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30400824 | ||||||
| chr17:30400952 | C | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.994+15716C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30400952 | |||||||
| chr17:30401200 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.994+15964C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401200 | |||||||
| chr17:30401230 | C | T | 1 | a0001c0001t0015g0271 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.994+15994C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401230 | |||||||
| chr17:30401247 | T | G | 1 | a0001c0001t0005g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.994+16011T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401247 | |||||||
| chr17:30401247 | TCTTCTC | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
132 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.994+16026_994+1603 others(10): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30401247 | ||||||
| chr17:30401288 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.994+16052C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401288 | |||||||
| chr17:30401302 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.994+16066A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401302 | |||||||
| chr17:30401339 | T | C | 10 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(7): Show |
11 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.994+16103T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401339 | |||||||
| chr17:30401373 | T | C | 1 | a0002c0002t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.994+16137T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401373 | |||||||
| chr17:30401383 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.994+16147C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401383 | |||||||
| chr17:30401429 | CTCT | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0026 others(13): Show |
18 | HG00438.hp2 HG00735.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.994+16202_994+1620 others(7): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30401429 | ||||||
| chr17:30401546 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.994+16310C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401546 | |||||||
| chr17:30401846 | T | C | 1 | a0001c0001t0009g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.994+16610T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401846 | |||||||
| chr17:30401939 | CT | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.994+16718delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30401939 | ||||||
| chr17:30401980 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.994+16744C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30401980 | |||||||
| chr17:30402073 | C | T | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.994+16837C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402073 | |||||||
| chr17:30402218 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.994+16982T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402218 | |||||||
| chr17:30402259 | A | T | 14 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(11): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.994+17023A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402259 | |||||||
| chr17:30402369 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.994+17133C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402369 | |||||||
| chr17:30402430 | G | T | 1 | a0001c0001t0002g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.994+17194G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402430 | |||||||
| chr17:30402449 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.994+17213C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402449 | |||||||
| chr17:30402622 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.994+17386T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402622 | |||||||
| chr17:30402753 | T | A | 1 | a0001c0001t0002g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.994+17517T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402753 | |||||||
| chr17:30402849 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.994+17613A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30402849 | |||||||
| chr17:30403123 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(129): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.995-17718A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403123 | |||||||
| chr17:30403294 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.995-17547C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403294 | |||||||
| chr17:30403354 | T | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-17487T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403354 | |||||||
| chr17:30403595 | G | A | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-17246G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403595 | |||||||
| chr17:30403602 | A | G | 1 | a0001c0001t0008g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.995-17239A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403602 | |||||||
| chr17:30403678 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.995-17163C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403678 | |||||||
| chr17:30403754 | C | T | 2 | a0001c0001t0002g0240 a0001c0001t0002g0245 |
2 | NA18957.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.995-17087C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403754 | |||||||
| chr17:30403842 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.995-16999C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403842 | |||||||
| chr17:30403919 | G | A | 1 | a0002c0002t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.995-16922G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30403919 | |||||||
| chr17:30403972 | CAA | C | 14 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(11): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-16866_995-1686 others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30403972 | ||||||
| chr17:30404244 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(217): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.995-16597G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30404244 | |||||||
| chr17:30404397 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-16444G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30404397 | |||||||
| chr17:30404704 | ATC | A | 47 | a0001c0001t0001g0204 a0001c0001t0002g0012 a0001c0001t0002g0013 others(44): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.995-16133_995-1613 others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30404704 | ||||||
| chr17:30405131 | G | A | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-15710G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405131 | |||||||
| chr17:30405170 | G | T | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.995-15671G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405170 | |||||||
| chr17:30405182 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.995-15659T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405182 | |||||||
| chr17:30405270 | T | C | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-15571T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405270 | |||||||
| chr17:30405476 | A | G | 2 | a0001c0001t0003g0145 a0001c0001t0003g0146 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.995-15365A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405476 | |||||||
| chr17:30405587 | A | G | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.995-15254A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405587 | |||||||
| chr17:30405723 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.995-15118C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405723 | |||||||
| chr17:30405857 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.995-14984T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30405857 | |||||||
| chr17:30406359 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.995-14482T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30406359 | |||||||
| chr17:30406419 | T | C | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.995-14422T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30406419 | |||||||
| chr17:30406652 | C | T | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.995-14189C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30406652 | |||||||
| chr17:30406839 | A | G | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-14002A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30406839 | |||||||
| chr17:30406844 | T | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0106 others(1): Show |
4 | HG00099.hp1 HG01169.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-13997T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30406844 | |||||||
| chr17:30407110 | T | C | 1 | a0002c0002t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.995-13731T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407110 | |||||||
| chr17:30407211 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-13630G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407211 | |||||||
| chr17:30407340 | A | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-13501A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407340 | |||||||
| chr17:30407395 | A | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.995-13446A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407395 | |||||||
| chr17:30407660 | G | T | 1 | a0002c0002t0001g0032 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.995-13181G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407660 | |||||||
| chr17:30407956 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.995-12885C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407956 | |||||||
| chr17:30407976 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-12865C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30407976 | |||||||
| chr17:30408021 | A | G | 4 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 others(1): Show |
4 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-12820A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408021 | |||||||
| chr17:30408322 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.995-12519A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408322 | |||||||
| chr17:30408415 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.995-12426G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408415 | |||||||
| chr17:30408461 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.995-12380T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408461 | |||||||
| chr17:30408603 | CTGTATGT others(3): Show |
C | 1 | a0001c0001t0007g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.995-12236_995-1222 others(14): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30408603 | ||||||
| chr17:30408802 | T | C | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.995-12039T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408802 | |||||||
| chr17:30408808 | T | C | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.995-12033T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408808 | |||||||
| chr17:30408814 | G | A | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.995-12027G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408814 | |||||||
| chr17:30408954 | G | A | 1 | a0001c0001t0005g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.995-11887G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408954 | |||||||
| chr17:30408995 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.995-11846T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30408995 | |||||||
| chr17:30409029 | C | T | 1 | a0001c0001t0027g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.995-11812C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409029 | |||||||
| chr17:30409086 | A | C | 1 | a0001c0001t0005g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.995-11755A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409086 | |||||||
| chr17:30409088 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
2 | NA18983.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.995-11753G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409088 | |||||||
| chr17:30409251 | C | A | 1 | a0001c0001t0002g0152 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.995-11590C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409251 | |||||||
| chr17:30409363 | CT | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.995-11477delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409363 | |||||||
| chr17:30409407 | T | G | 9 | a0001c0004t0002g0198 a0001c0004t0002g0201 a0001c0004t0002g0224 others(6): Show |
9 | HG00597.hp1 HG02683.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-11434T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409407 | |||||||
| chr17:30409410 | T | C | 1 | a0001c0001t0022g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.995-11431T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409410 | |||||||
| chr17:30409470 | G | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-11371G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409470 | |||||||
| chr17:30409598 | C | T | 47 | a0001c0001t0001g0204 a0001c0001t0002g0012 a0001c0001t0002g0013 others(44): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.995-11243C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409598 | |||||||
| chr17:30409748 | CTTCTTT | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-11092_995-1108 others(10): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409748 | |||||||
| chr17:30409764 | G | T | 1 | a0001c0001t0002g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.995-11077G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409764 | |||||||
| chr17:30409902 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.995-10939T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30409902 | |||||||
| chr17:30410216 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0106 |
2 | HG00099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.995-10625G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30410216 | |||||||
| chr17:30410839 | A | G | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.995-10002A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30410839 | |||||||
| chr17:30410950 | C | CATGA | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(138): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.995-9887_995-9884d others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30410950 | ||||||
| chr17:30411002 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-9839C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30411002 | |||||||
| chr17:30411622 | G | T | 5 | a0001c0001t0003g0011 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
6 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-9219G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30411622 | |||||||
| chr17:30411685 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.995-9156C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30411685 | |||||||
| chr17:30411804 | A | G | 1 | a0002c0002t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.995-9037A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30411804 | |||||||
| chr17:30412189 | CTGCAGAA others(10): Show |
C | 1 | a0001c0001t0021g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.995-8631_995-8615d others(19): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30412189 | ||||||
| chr17:30412335 | G | A | 1 | a0001c0001t0004g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.995-8506G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30412335 | |||||||
| chr17:30412426 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.995-8415C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30412426 | |||||||
| chr17:30412667 | G | A | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.995-8174G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30412667 | |||||||
| chr17:30412750 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.995-8091G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30412750 | |||||||
| chr17:30412847 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.995-7994C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30412847 | |||||||
| chr17:30413200 | A | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
6 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-7641A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413200 | |||||||
| chr17:30413234 | C | T | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.995-7607C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413234 | |||||||
| chr17:30413477 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.995-7364A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413477 | |||||||
| chr17:30413514 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.995-7327G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413514 | |||||||
| chr17:30413617 | A | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.995-7224A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413617 | |||||||
| chr17:30413905 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-6936G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413905 | |||||||
| chr17:30413971 | A | G | 2 | a0001c0006t0002g0025 a0001c0006t0002g0202 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.995-6870A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30413971 | |||||||
| chr17:30414046 | G | A | 2 | a0001c0001t0003g0148 a0001c0001t0003g0151 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.995-6795G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414046 | |||||||
| chr17:30414239 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.995-6602A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414239 | |||||||
| chr17:30414396 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.995-6445A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414396 | |||||||
| chr17:30414452 | G | A | 1 | a0005c0013t0002g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.995-6389G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414452 | |||||||
| chr17:30414582 | G | GA | 7 | a0001c0001t0001g0123 a0001c0001t0002g0215 a0001c0001t0003g0143 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.995-6245dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30414582 | ||||||
| chr17:30414635 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.995-6206C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414635 | |||||||
| chr17:30414654 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.995-6187A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414654 | |||||||
| chr17:30414657 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.995-6184G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414657 | |||||||
| chr17:30414963 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.995-5878G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30414963 | |||||||
| chr17:30414983 | G | GT | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.995-5855dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30414983 | ||||||
| chr17:30415104 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.995-5737C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30415104 | |||||||
| chr17:30415118 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-5723A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30415118 | |||||||
| chr17:30415428 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.995-5413C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30415428 | |||||||
| chr17:30415454 | A | C | 2 | a0001c0001t0003g0148 a0001c0001t0003g0151 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.995-5387A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30415454 | |||||||
| chr17:30415755 | G | T | 1 | a0001c0001t0002g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.995-5086G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30415755 | |||||||
| chr17:30416009 | T | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0078 a0001c0001t0001g0098 others(3): Show |
6 | HG00673.hp1 HG03669.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-4832T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416009 | |||||||
| chr17:30416101 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0001g0129 others(5): Show |
9 | HG01175.hp1 HG01891.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-4740G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416101 | |||||||
| chr17:30416103 | C | T | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-4738C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416103 | |||||||
| chr17:30416130 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.995-4711C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416130 | |||||||
| chr17:30416138 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.995-4703G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416138 | |||||||
| chr17:30416175 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.995-4666A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416175 | |||||||
| chr17:30416273 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.995-4568G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416273 | |||||||
| chr17:30416359 | T | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-4482T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416359 | |||||||
| chr17:30416418 | A | C | 1 | a0001c0004t0002g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.995-4423A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416418 | |||||||
| chr17:30416419 | T | C | 1 | a0001c0001t0009g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.995-4422T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416419 | |||||||
| chr17:30416622 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.995-4219T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30416622 | |||||||
| chr17:30417101 | C | CA | 12 | a0001c0001t0001g0062 a0001c0001t0001g0109 a0001c0001t0003g0011 others(9): Show |
13 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.995-3725dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30417101 | ||||||
| chr17:30417244 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.995-3597A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417244 | |||||||
| chr17:30417250 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-3591C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417250 | |||||||
| chr17:30417347 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.995-3494G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417347 | |||||||
| chr17:30417510 | T | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-3331T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417510 | |||||||
| chr17:30417702 | G | A | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.995-3139G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417702 | |||||||
| chr17:30417728 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.995-3113G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417728 | |||||||
| chr17:30417754 | C | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(139): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.995-3087C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30417754 | |||||||
| chr17:30418040 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.995-2801C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418040 | |||||||
| chr17:30418180 | A | AT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.995-2654dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30418180 | ||||||
| chr17:30418383 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-2458A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418383 | |||||||
| chr17:30418461 | A | G | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.995-2380A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418461 | |||||||
| chr17:30418592 | T | TGTA | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-2248_995-2246d others(5): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30418592 | ||||||
| chr17:30418597 | C | G | 3 | a0001c0001t0009g0022 a0001c0001t0009g0023 a0001c0001t0009g0024 |
3 | HG01192.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.995-2244C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418597 | |||||||
| chr17:30418747 | T | A | 5 | a0001c0004t0002g0198 a0001c0004t0002g0201 a0001c0004t0002g0224 others(2): Show |
5 | HG00597.hp1 HG02683.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.995-2094T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418747 | |||||||
| chr17:30418786 | A | G | 6 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0089 others(3): Show |
6 | HG02027.hp1 HG02135.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-2055A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418786 | |||||||
| chr17:30418851 | G | T | 1 | a0001c0001t0003g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.995-1990G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30418851 | |||||||
| chr17:30419217 | T | C | 6 | a0001c0001t0002g0162 a0001c0001t0002g0182 a0001c0001t0002g0183 others(3): Show |
6 | NA18951.hp2 NA18972.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1624T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30419217 | |||||||
| chr17:30419386 | C | T | 26 | a0001c0001t0001g0204 a0001c0001t0002g0012 a0001c0001t0002g0013 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.995-1455C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30419386 | |||||||
| chr17:30419395 | A | G | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1446A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30419395 | |||||||
| chr17:30419530 | A | G | 1 | a0011c0011t0008g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.995-1311A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30419530 | |||||||
| chr17:30419587 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.995-1254C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30419587 | |||||||
| chr17:30419624 | GGCCATT | G | 10 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(7): Show |
11 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-1214_995-1209d others(8): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30419624 | ||||||
| chr17:30419654 | ATTTT | A | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 |
3 | HG01192.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.995-1185_995-1182d others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 30419654 | ||||||
| chr17:30419926 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.995-915C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30419926 | |||||||
| chr17:30420222 | T | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.995-619T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30420222 | |||||||
| chr17:30420329 | G | A | 1 | a0001c0001t0005g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.995-512G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30420329 | |||||||
| chr17:30420476 | T | A | 1 | a0001c0006t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995-365T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30420476 | |||||||
| chr17:30420755 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.995-86A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30420755 | |||||||
| chr17:30420832 | A | G | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-9A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 2/20 | chr17 | 30420832 | |||||||
| chr17:30421174 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1137+191T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 3/20 | chr17 | 30421174 | |||||||
| chr17:30421334 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1138-330A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 3/20 | chr17 | 30421334 | |||||||
| chr17:30421481 | T | C | 1 | a0006c0014t0002g0209 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1138-183T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 3/20 | chr17 | 30421481 | |||||||
| chr17:30421500 | A | C | 2 | a0001c0001t0003g0145 a0001c0001t0003g0146 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-164A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 3/20 | chr17 | 30421500 | |||||||
| chr17:30422012 | T | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307+179T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 4/20 | chr17 | 30422012 | |||||||
| chr17:30422451 | T | A | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1308-223T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 4/20 | chr17 | 30422451 | |||||||
| chr17:30422457 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0139 |
2 | HG01175.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1308-217A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 4/20 | chr17 | 30422457 | |||||||
| chr17:30422653 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1308-21T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 4/20 | chr17 | 30422653 | |||||||
| chr17:30423217 | C | A | 1 | a0001c0001t0002g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1657+194C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 5/20 | chr17 | 30423217 | |||||||
| chr17:30423305 | A | G | 1 | a0001c0001t0002g0193 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1658-201A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 5/20 | chr17 | 30423305 | |||||||
| chr17:30423448 | T | TGAGTCCA others(24): Show |
1 | a0001c0001t0005g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1658-57_1658-27dup others(31): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 30423448 | ||||||
| chr17:30423924 | A | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1849+227A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30423924 | |||||||
| chr17:30424104 | T | TGCAGCTT others(338): Show |
1 | a0001c0001t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1849+420_1849+421i others(347): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30424104 | ||||||
| chr17:30424145 | A | C | 1 | a0001c0001t0002g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1849+448A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30424145 | |||||||
| chr17:30424458 | T | C | 1 | a0001c0001t0012g0237 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1849+761T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30424458 | |||||||
| chr17:30424599 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1849+902A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30424599 | |||||||
| chr17:30424973 | C | G | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849+1276C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30424973 | |||||||
| chr17:30425125 | CTT | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(124): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1849+1429_1849+143 others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30425125 | |||||||
| chr17:30425305 | C | T | 1 | a0001c0001t0021g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1849+1608C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30425305 | |||||||
| chr17:30425325 | A | G | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849+1628A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30425325 | |||||||
| chr17:30425517 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1849+1820G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30425517 | |||||||
| chr17:30425655 | CA | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1850-1719delA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30425655 | ||||||
| chr17:30425731 | A | G | 2 | a0001c0001t0001g0124 a0004c0007t0001g0125 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1850-1660A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30425731 | |||||||
| chr17:30425945 | C | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1850-1446C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30425945 | |||||||
| chr17:30426050 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(108): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1850-1341A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426050 | |||||||
| chr17:30426165 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1850-1226A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426165 | |||||||
| chr17:30426194 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-1197C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426194 | |||||||
| chr17:30426195 | G | A | 2 | a0001c0001t0004g0037 a0001c0001t0004g0038 |
2 | HG00140.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1850-1196G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426195 | |||||||
| chr17:30426195 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1850-1196G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426195 | |||||||
| chr17:30426199 | C | CA | 17 | a0001c0001t0001g0204 a0001c0001t0002g0163 a0001c0001t0002g0174 others(14): Show |
18 | HG01106.hp1 HG01433.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1850-1172dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30426199 | ||||||
| chr17:30426199 | CA | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1850-1172delA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30426199 | ||||||
| chr17:30426199 | CAA | C | 8 | a0001c0001t0001g0080 a0001c0001t0001g0113 a0001c0001t0001g0261 others(5): Show |
8 | HG01993.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-1173_1850-117 others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30426199 | ||||||
| chr17:30426288 | G | T | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1850-1103G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426288 | |||||||
| chr17:30426462 | G | A | 10 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(7): Show |
11 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1850-929G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426462 | |||||||
| chr17:30426552 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1850-839G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426552 | |||||||
| chr17:30426607 | G | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1850-784G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426607 | |||||||
| chr17:30426762 | G | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1850-629G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426762 | |||||||
| chr17:30426818 | CTAAA | C | 3 | a0001c0001t0005g0267 a0001c0001t0005g0269 a0001c0001t0005g0270 |
3 | HG02572.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1850-571_1850-568d others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30426818 | ||||||
| chr17:30426902 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(155): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1850-489T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30426902 | |||||||
| chr17:30427138 | C | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850-253C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30427138 | |||||||
| chr17:30427163 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1850-228C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | chr17 | 30427163 | |||||||
| chr17:30427181 | C | CA | 8 | a0001c0001t0001g0026 a0001c0001t0001g0057 a0001c0001t0001g0073 others(5): Show |
8 | HG01109.hp1 HG02135.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1850-195dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 30427181 | ||||||
| chr17:30427563 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | splice_region_variant&intron_variant | LOW | c.2017+5G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30427563 | |||||||
| chr17:30427617 | T | G | 1 | a0001c0001t0004g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2017+59T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30427617 | |||||||
| chr17:30427748 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2017+190T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30427748 | |||||||
| chr17:30427808 | C | T | 1 | a0001c0001t0005g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2017+250C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30427808 | |||||||
| chr17:30427987 | A | C | 5 | a0001c0001t0006g0121 a0001c0001t0006g0122 a0001c0001t0006g0126 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+429A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30427987 | |||||||
| chr17:30428006 | T | G | 1 | a0001c0001t0002g0193 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2017+448T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30428006 | |||||||
| chr17:30428074 | T | C | 1 | a0001c0004t0002g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2017+516T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30428074 | |||||||
| chr17:30428436 | C | G | 1 | a0001c0001t0019g0246 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2017+878C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30428436 | |||||||
| chr17:30428449 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+891A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30428449 | |||||||
| chr17:30428641 | A | T | 1 | a0001c0001t0009g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2017+1083A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30428641 | |||||||
| chr17:30428730 | G | A | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+1172G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30428730 | |||||||
| chr17:30428882 | T | TA | 20 | a0001c0001t0001g0097 a0001c0001t0001g0254 a0001c0001t0001g0256 others(17): Show |
21 | HG01256.hp2 HG01433.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2017+1336dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | 30428882 | ||||||
| chr17:30428882 | T | TAA | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(125): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2017+1335_2017+133 others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | 30428882 | ||||||
| chr17:30429131 | T | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2017+1573T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30429131 | |||||||
| chr17:30429393 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0069 others(7): Show |
10 | HG00735.hp2 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.2017+1835C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30429393 | |||||||
| chr17:30430021 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2018-1751G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30430021 | |||||||
| chr17:30430286 | C | G | 3 | a0001c0001t0010g0156 a0001c0001t0010g0157 a0001c0001t0010g0158 |
3 | HG01243.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2018-1486C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30430286 | |||||||
| chr17:30430292 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2018-1480T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30430292 | |||||||
| chr17:30430400 | G | A | 1 | a0004c0007t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2018-1372G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30430400 | |||||||
| chr17:30430421 | G | A | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-1351G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30430421 | |||||||
| chr17:30430914 | C | G | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 |
3 | HG01192.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2018-858C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30430914 | |||||||
| chr17:30431152 | G | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 |
4 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-620G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30431152 | |||||||
| chr17:30431352 | G | A | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-420G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30431352 | |||||||
| chr17:30431592 | A | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2018-180A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 7/20 | chr17 | 30431592 | |||||||
| chr17:30432010 | C | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2127+129C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30432010 | |||||||
| chr17:30432017 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.2127+136T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30432017 | |||||||
| chr17:30432077 | C | G | 2 | a0001c0001t0002g0203 a0001c0001t0002g0220 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2127+196C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30432077 | |||||||
| chr17:30432315 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2127+434G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30432315 | |||||||
| chr17:30433089 | T | C | 1 | a0001c0001t0002g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2127+1208T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433089 | |||||||
| chr17:30433161 | G | A | 2 | a0001c0001t0002g0240 a0001c0001t0002g0245 |
2 | NA18957.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2127+1280G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433161 | |||||||
| chr17:30433315 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2127+1434A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433315 | |||||||
| chr17:30433589 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2127+1708T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433589 | |||||||
| chr17:30433657 | T | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0106 others(1): Show |
4 | HG00099.hp1 HG01169.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2127+1776T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433657 | |||||||
| chr17:30433713 | A | G | 1 | a0004c0007t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2127+1832A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433713 | |||||||
| chr17:30433921 | C | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2127+2040C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433921 | |||||||
| chr17:30433949 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2127+2068A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30433949 | |||||||
| chr17:30434104 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0098 |
2 | HG00673.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2127+2223A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434104 | |||||||
| chr17:30434108 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2127+2227T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434108 | |||||||
| chr17:30434123 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2127+2242A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434123 | |||||||
| chr17:30434165 | T | C | 9 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
9 | HG01070.hp1 HG01952.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.2127+2284T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434165 | |||||||
| chr17:30434295 | T | A | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2127+2414T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434295 | |||||||
| chr17:30434296 | A | T | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2127+2415A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434296 | |||||||
| chr17:30434363 | G | A | 1 | a0001c0001t0024g0112 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2127+2482G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434363 | |||||||
| chr17:30434605 | T | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(8): Show |
12 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2127+2724T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434605 | |||||||
| chr17:30434607 | G | A | 2 | a0001c0001t0002g0205 a0001c0001t0002g0217 |
2 | HG00738.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2127+2726G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434607 | |||||||
| chr17:30434717 | A | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.2127+2836A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434717 | |||||||
| chr17:30434829 | A | G | 4 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 others(1): Show |
4 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2127+2948A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434829 | |||||||
| chr17:30434966 | C | T | 3 | a0001c0001t0002g0203 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG02615.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2127+3085C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434966 | |||||||
| chr17:30434974 | A | G | 1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2127+3093A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30434974 | |||||||
| chr17:30435091 | A | G | 8 | a0001c0001t0001g0204 a0001c0001t0002g0197 a0001c0001t0002g0200 others(5): Show |
8 | HG00738.hp1 HG01074.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2127+3210A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435091 | |||||||
| chr17:30435318 | G | GCATGACT others(195): Show |
1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2127+3437_2127+343 others(206): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435318 | |||||||
| chr17:30435321 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2127+3440A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435321 | |||||||
| chr17:30435322 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2127+3441T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435322 | |||||||
| chr17:30435324 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2127+3443G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435324 | |||||||
| chr17:30435329 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2127+3448G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435329 | |||||||
| chr17:30435331 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2127+3450G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435331 | |||||||
| chr17:30435334 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2127+3453C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435334 | |||||||
| chr17:30435368 | AT | A | 12 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(9): Show |
12 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2127+3498delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 30435368 | ||||||
| chr17:30435536 | A | G | 1 | a0001c0001t0004g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2128-3439A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435536 | |||||||
| chr17:30435763 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2128-3212C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30435763 | |||||||
| chr17:30436293 | A | G | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2128-2682A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30436293 | |||||||
| chr17:30436653 | A | G | 1 | a0001c0001t0002g0004 | 3 | NA18983.hp2 NA19003.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2128-2322A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30436653 | |||||||
| chr17:30436790 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2128-2185A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30436790 | |||||||
| chr17:30437133 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.2128-1842G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437133 | |||||||
| chr17:30437409 | G | A | 7 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0031 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2128-1566G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437409 | |||||||
| chr17:30437451 | G | T | 4 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0002g0193 others(1): Show |
4 | HG01070.hp1 HG01952.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.2128-1524G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437451 | |||||||
| chr17:30437470 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0115 |
2 | HG01106.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2128-1505A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437470 | |||||||
| chr17:30437607 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2128-1368C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437607 | |||||||
| chr17:30437774 | AAG | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2128-1196_2128-119 others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 30437774 | ||||||
| chr17:30437861 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2128-1114G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437861 | |||||||
| chr17:30437879 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2128-1096C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30437879 | |||||||
| chr17:30438000 | C | CT | 71 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0056 others(68): Show |
72 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2128-951dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 30438000 | ||||||
| chr17:30438091 | A | G | 1 | a0003c0016t0001g0053 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2128-884A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438091 | |||||||
| chr17:30438142 | G | T | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2128-833G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438142 | |||||||
| chr17:30438750 | T | G | 1 | a0001c0001t0002g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2128-225T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438750 | |||||||
| chr17:30438916 | T | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-59T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438916 | |||||||
| chr17:30438917 | A | AT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0067 a0001c0001t0001g0093 others(4): Show |
7 | HG01106.hp2 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2128-49dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 30438917 | ||||||
| chr17:30438919 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-56T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438919 | |||||||
| chr17:30438920 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-55T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438920 | |||||||
| chr17:30438922 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-53T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438922 | |||||||
| chr17:30438923 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-52T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438923 | |||||||
| chr17:30438924 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-51T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438924 | |||||||
| chr17:30438925 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-50T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438925 | |||||||
| chr17:30438926 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-49T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438926 | |||||||
| chr17:30438927 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2128-48G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 8/20 | chr17 | 30438927 | |||||||
| chr17:30439287 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2230+210A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439287 | |||||||
| chr17:30439294 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2230+217G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439294 | |||||||
| chr17:30439368 | C | CTTTTT | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2230+295_2230+299d others(7): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr17 | 30439368 | ||||||
| chr17:30439394 | C | CT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(159): Show |
170 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.2230+330dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr17 | 30439394 | ||||||
| chr17:30439430 | T | C | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2230+353T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439430 | |||||||
| chr17:30439501 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2230+424G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439501 | |||||||
| chr17:30439560 | C | A | 1 | a0002c0002t0001g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2230+483C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439560 | |||||||
| chr17:30439565 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2230+488C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439565 | |||||||
| chr17:30439677 | C | T | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2230+600C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439677 | |||||||
| chr17:30439723 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2230+646G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439723 | |||||||
| chr17:30439804 | A | G | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2230+727A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439804 | |||||||
| chr17:30439905 | G | C | 1 | a0001c0001t0002g0185 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2230+828G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439905 | |||||||
| chr17:30439931 | G | A | 1 | a0001c0001t0027g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2230+854G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30439931 | |||||||
| chr17:30440235 | C | T | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2230+1158C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440235 | |||||||
| chr17:30440236 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0119 |
2 | HG03491.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2230+1159G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440236 | |||||||
| chr17:30440312 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(8): Show |
12 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2230+1235C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440312 | |||||||
| chr17:30440384 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0060 others(2): Show |
7 | HG00438.hp1 HG02056.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2230+1307C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440384 | |||||||
| chr17:30440415 | T | G | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2230+1338T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440415 | |||||||
| chr17:30440437 | T | G | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2230+1360T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440437 | |||||||
| chr17:30440491 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2230+1414A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440491 | |||||||
| chr17:30440603 | G | C | 4 | a0001c0004t0002g0198 a0001c0004t0002g0201 a0001c0004t0002g0228 others(1): Show |
4 | HG02683.hp1 NA18954.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2230+1526G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440603 | |||||||
| chr17:30440807 | C | G | 14 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(11): Show |
15 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.2231-1501C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440807 | |||||||
| chr17:30440820 | G | A | 3 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG03490.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2231-1488G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440820 | |||||||
| chr17:30440968 | G | T | 2 | a0001c0006t0002g0025 a0001c0006t0002g0202 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2231-1340G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30440968 | |||||||
| chr17:30441005 | T | C | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2231-1303T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441005 | |||||||
| chr17:30441018 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2231-1290A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441018 | |||||||
| chr17:30441444 | T | C | 4 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 others(1): Show |
4 | NA18972.hp1 NA18974.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2231-864T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441444 | |||||||
| chr17:30441451 | A | C | 1 | a0001c0005t0001g0008 | 2 | HG01169.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2231-857A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441451 | |||||||
| chr17:30441535 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2231-773T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441535 | |||||||
| chr17:30441580 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2231-728G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441580 | |||||||
| chr17:30441616 | A | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
6 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2231-692A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441616 | |||||||
| chr17:30441724 | C | T | 28 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(25): Show |
31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.2231-584C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441724 | |||||||
| chr17:30441836 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.2231-472C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441836 | |||||||
| chr17:30441924 | A | T | 1 | a0001c0001t0003g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2231-384A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30441924 | |||||||
| chr17:30442153 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2231-155A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30442153 | |||||||
| chr17:30442156 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2231-152G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30442156 | |||||||
| chr17:30442180 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2231-128G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 9/20 | chr17 | 30442180 | |||||||
| chr17:30442571 | A | G | 1 | a0001c0001t0004g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2373+121A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 10/20 | chr17 | 30442571 | |||||||
| chr17:30443007 | G | GT | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.2373+565dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | 30443007 | ||||||
| chr17:30443082 | A | C | 1 | a0001c0001t0021g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2373+632A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 10/20 | chr17 | 30443082 | |||||||
| chr17:30443981 | T | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2543+10T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30443981 | |||||||
| chr17:30444079 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2543+108G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30444079 | |||||||
| chr17:30444089 | G | A | 1 | a0001c0001t0007g0272 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2543+118G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30444089 | |||||||
| chr17:30444477 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(171): Show |
183 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2543+506T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30444477 | |||||||
| chr17:30444516 | C | CT | 37 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0066 others(34): Show |
38 | HG00597.hp1 HG00738.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.2543+571dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr17 | 30444516 | ||||||
| chr17:30444516 | C | CTT | 6 | a0001c0001t0002g0159 a0001c0001t0002g0162 a0001c0001t0002g0194 others(3): Show |
6 | NA18951.hp2 NA18960.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.2543+570_2543+571d others(4): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr17 | 30444516 | ||||||
| chr17:30444516 | CT | C | 13 | a0001c0001t0001g0107 a0001c0001t0002g0186 a0001c0001t0002g0188 others(10): Show |
14 | HG01070.hp1 HG01346.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.2543+571delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr17 | 30444516 | ||||||
| chr17:30444645 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2543+674T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30444645 | |||||||
| chr17:30444685 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(125): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2543+714G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30444685 | |||||||
| chr17:30445076 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2544-615G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30445076 | |||||||
| chr17:30445178 | A | G | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2544-513A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30445178 | |||||||
| chr17:30445343 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.2544-348C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30445343 | |||||||
| chr17:30445548 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2544-143T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 11/20 | chr17 | 30445548 | |||||||
| chr17:30446042 | CT | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0254 others(6): Show |
9 | HG01515.hp1 HG02109.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2873+35delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr17 | 30446042 | ||||||
| chr17:30446097 | A | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0179 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2873+77A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30446097 | |||||||
| chr17:30446229 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2873+209G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30446229 | |||||||
| chr17:30446283 | G | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(8): Show |
12 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2873+263G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30446283 | |||||||
| chr17:30446425 | G | A | 1 | a0001c0001t0006g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2873+405G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30446425 | |||||||
| chr17:30446745 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(24): Show |
30 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2873+725T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30446745 | |||||||
| chr17:30446828 | C | T | 4 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0145 others(1): Show |
4 | HG02486.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2873+808C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30446828 | |||||||
| chr17:30447049 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2873+1029A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447049 | |||||||
| chr17:30447202 | G | T | 1 | a0001c0001t0002g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2873+1182G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447202 | |||||||
| chr17:30447212 | G | C | 5 | a0001c0001t0006g0121 a0001c0001t0006g0122 a0001c0001t0006g0126 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2873+1192G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447212 | |||||||
| chr17:30447278 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2873+1258A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447278 | |||||||
| chr17:30447344 | A | G | 1 | a0002c0002t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2873+1324A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447344 | |||||||
| chr17:30447415 | G | T | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 |
3 | HG01192.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2873+1395G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447415 | |||||||
| chr17:30447665 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2873+1645T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447665 | |||||||
| chr17:30447909 | T | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 |
4 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2874-1644T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30447909 | |||||||
| chr17:30448375 | A | T | 1 | a0005c0013t0002g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2874-1178A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448375 | |||||||
| chr17:30448548 | G | A | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00738.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2874-1005G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448548 | |||||||
| chr17:30448557 | A | C | 1 | a0001c0001t0006g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2874-996A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448557 | |||||||
| chr17:30448679 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874-874A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448679 | |||||||
| chr17:30448836 | C | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2874-717C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448836 | |||||||
| chr17:30448837 | G | A | 1 | a0003c0017t0016g0051 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2874-716G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448837 | |||||||
| chr17:30448953 | A | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0001g0129 others(7): Show |
11 | HG01175.hp1 HG01891.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2874-600A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448953 | |||||||
| chr17:30448969 | A | G | 1 | a0001c0001t0007g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2874-584A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30448969 | |||||||
| chr17:30449129 | T | TATAA | 8 | a0001c0001t0007g0272 a0002c0002t0001g0028 a0002c0002t0001g0029 others(5): Show |
8 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2874-403_2874-400d others(6): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr17 | 30449129 | ||||||
| chr17:30449129 | T | TATAAATA others(1): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0259 |
3 | NA18947.hp2 NA18983.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2874-407_2874-400d others(10): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr17 | 30449129 | ||||||
| chr17:30449129 | TATAAATA others(1): Show |
T | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG01255.hp1 HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2874-407_2874-400d others(10): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr17 | 30449129 | ||||||
| chr17:30449159 | G | A | 1 | a0001c0001t0009g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2874-394G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30449159 | |||||||
| chr17:30449245 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2874-308T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30449245 | |||||||
| chr17:30449325 | TAATCTTT others(4): Show |
T | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2874-211_2874-201d others(13): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr17 | 30449325 | ||||||
| chr17:30449367 | T | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(8): Show |
12 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2874-186T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 12/20 | chr17 | 30449367 | |||||||
| chr17:30449830 | A | T | 1 | a0001c0001t0002g0244 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3069+82A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30449830 | |||||||
| chr17:30449935 | A | G | 6 | a0001c0004t0002g0198 a0001c0004t0002g0201 a0001c0004t0002g0224 others(3): Show |
6 | HG00597.hp1 HG02683.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.3069+187A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30449935 | |||||||
| chr17:30450057 | CT | C | 6 | a0001c0001t0002g0152 a0001c0001t0003g0011 a0001c0001t0003g0147 others(3): Show |
7 | HG01256.hp1 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3069+326delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | 30450057 | ||||||
| chr17:30450117 | CATGATCT others(106): Show |
C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0016 a0001c0001t0014g0017 others(1): Show |
5 | HG02622.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3069+372_3069+484d others(2): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | 30450117 | ||||||
| chr17:30450152 | A | C | 1 | a0001c0001t0002g0163 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3069+404A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30450152 | |||||||
| chr17:30450248 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3069+500G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30450248 | |||||||
| chr17:30450306 | C | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.3069+558C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30450306 | |||||||
| chr17:30450784 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3070-927A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30450784 | |||||||
| chr17:30450859 | C | CAAACA | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3070-837_3070-833d others(7): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | 30450859 | ||||||
| chr17:30451040 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0139 |
3 | HG01175.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3070-671G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30451040 | |||||||
| chr17:30451171 | G | T | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3070-540G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30451171 | |||||||
| chr17:30451688 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0104 |
2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3070-23G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30451688 | |||||||
| chr17:30451702 | G | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.3070-9G>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 13/20 | chr17 | 30451702 | |||||||
| chr17:30452037 | T | G | 1 | a0001c0001t0022g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3205+191T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30452037 | |||||||
| chr17:30452150 | G | A | 1 | a0001c0001t0021g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3205+304G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30452150 | |||||||
| chr17:30452282 | C | CT | 16 | a0001c0001t0002g0205 a0001c0001t0003g0011 a0001c0001t0003g0142 others(13): Show |
17 | HG00738.hp1 HG01192.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.3205+450dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr17 | 30452282 | ||||||
| chr17:30452499 | C | T | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 |
3 | HG01192.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3205+653C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30452499 | |||||||
| chr17:30452603 | A | G | 1 | a0001c0001t0027g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3205+757A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30452603 | |||||||
| chr17:30452760 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3205+914C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30452760 | |||||||
| chr17:30452893 | A | G | 1 | a0001c0001t0002g0014 | 2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3205+1047A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30452893 | |||||||
| chr17:30453011 | C | T | 10 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(7): Show |
11 | HG01433.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3205+1165C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30453011 | |||||||
| chr17:30453102 | C | A | 1 | a0001c0001t0007g0272 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3205+1256C>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30453102 | |||||||
| chr17:30453160 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0110 a0001c0001t0011g0087 others(2): Show |
5 | HG01109.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.3205+1314G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30453160 | |||||||
| chr17:30453209 | A | G | 3 | a0001c0001t0001g0254 a0001c0001t0001g0257 a0001c0001t0003g0255 |
3 | HG02109.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3205+1363A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30453209 | |||||||
| chr17:30453515 | G | A | 1 | a0001c0001t0005g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3205+1669G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30453515 | |||||||
| chr17:30454005 | C | T | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 |
3 | HG01192.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3206-1334C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454005 | |||||||
| chr17:30454051 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3206-1288G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454051 | |||||||
| chr17:30454703 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3206-636C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454703 | |||||||
| chr17:30454774 | G | A | 48 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.3206-565G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454774 | |||||||
| chr17:30454908 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3206-431C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454908 | |||||||
| chr17:30454909 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0178 a0001c0001t0002g0187 |
5 | HG02027.hp2 HG02083.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.3206-430G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454909 | |||||||
| chr17:30454926 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3206-413A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30454926 | |||||||
| chr17:30455129 | A | G | 1 | a0001c0005t0001g0008 | 2 | HG01169.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3206-210A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30455129 | |||||||
| chr17:30455317 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3206-22A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 14/20 | chr17 | 30455317 | |||||||
| chr17:30455972 | C | T | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3338-284C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 15/20 | chr17 | 30455972 | |||||||
| chr17:30456135 | A | T | 1 | a0001c0001t0002g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3338-121A>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 15/20 | chr17 | 30456135 | |||||||
| chr17:30456231 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3338-25G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 15/20 | chr17 | 30456231 | |||||||
| chr17:30456584 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0060 |
2 | NA18992.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3498+58G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30456584 | |||||||
| chr17:30456846 | C | CA | 27 | a0001c0001t0002g0175 a0001c0001t0002g0179 a0001c0001t0002g0184 others(24): Show |
29 | HG01192.hp2 HG01346.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.3498+343dupA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30456846 | ||||||
| chr17:30456846 | CA | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(108): Show |
117 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.3498+343delA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30456846 | ||||||
| chr17:30456846 | CAA | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG00099.hp1 HG03195.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.3498+342_3498+343d others(4): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30456846 | ||||||
| chr17:30457364 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.3498+838A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30457364 | |||||||
| chr17:30457590 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3498+1064T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30457590 | |||||||
| chr17:30457665 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3498+1139G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30457665 | |||||||
| chr17:30457809 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0075 |
3 | NA19003.hp1 NA19074.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3498+1283G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30457809 | |||||||
| chr17:30457915 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3498+1389C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30457915 | |||||||
| chr17:30458203 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3498+1677G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30458203 | |||||||
| chr17:30458354 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3498+1828C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30458354 | |||||||
| chr17:30458511 | G | A | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3498+1985G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30458511 | |||||||
| chr17:30458737 | G | A | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3498+2211G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30458737 | |||||||
| chr17:30458851 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0001g0129 others(5): Show |
9 | HG01175.hp1 HG01891.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3498+2325G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30458851 | |||||||
| chr17:30458865 | CA | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(216): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.3499-2301delA | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30458865 | ||||||
| chr17:30459102 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3499-2078A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30459102 | |||||||
| chr17:30459146 | C | CT | 31 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0072 others(28): Show |
33 | HG00438.hp1 HG00544.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.3499-2016dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30459146 | ||||||
| chr17:30459146 | CT | C | 52 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0084 others(49): Show |
55 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.3499-2016delT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30459146 | ||||||
| chr17:30459178 | C | CT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.3499-1994dupT | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30459178 | ||||||
| chr17:30459199 | ATTTATT | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0129 a0001c0001t0011g0103 others(1): Show |
4 | HG01358.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3499-1973_3499-196 others(10): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30459199 | ||||||
| chr17:30459206 | T | TA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.3499-1974_3499-197 others(5): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30459206 | |||||||
| chr17:30459206 | TTTATTTA others(7): Show |
T | 1 | a0001c0001t0002g0154 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3499-1957_3499-194 others(18): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30459206 | ||||||
| chr17:30459596 | A | AGCTTTAT others(75): Show |
1 | a0001c0001t0001g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3499-1570_3499-156 others(86): Show |
CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 30459596 | ||||||
| chr17:30459716 | G | T | 1 | a0001c0001t0009g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3499-1464G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30459716 | |||||||
| chr17:30459861 | G | A | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3499-1319G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30459861 | |||||||
| chr17:30460016 | C | T | 2 | a0001c0001t0009g0022 a0001c0001t0009g0023 |
2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3499-1164C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30460016 | |||||||
| chr17:30460087 | T | G | 11 | a0001c0001t0003g0011 a0001c0001t0003g0143 a0001c0001t0003g0144 others(8): Show |
12 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3499-1093T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30460087 | |||||||
| chr17:30460129 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3499-1051T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30460129 | |||||||
| chr17:30460856 | C | T | 7 | a0001c0001t0004g0035 a0001c0001t0004g0039 a0001c0001t0004g0041 others(4): Show |
7 | HG00438.hp2 HG00673.hp2 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.3499-324C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30460856 | |||||||
| chr17:30460982 | C | T | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3499-198C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30460982 | |||||||
| chr17:30460983 | T | A | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3499-197T>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 17/20 | chr17 | 30460983 | |||||||
| chr17:30461403 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3630+92A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461403 | |||||||
| chr17:30461454 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3630+143T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461454 | |||||||
| chr17:30461568 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(135): Show |
145 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.3630+257G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461568 | |||||||
| chr17:30461602 | T | G | 4 | a0001c0001t0002g0160 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3631-275T>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461602 | |||||||
| chr17:30461604 | G | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(272): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3631-273G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461604 | |||||||
| chr17:30461700 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3631-177G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461700 | |||||||
| chr17:30461719 | G | A | 1 | a0001c0001t0012g0208 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3631-158G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461719 | |||||||
| chr17:30461761 | T | C | 3 | a0001c0001t0002g0189 a0001c0001t0002g0195 a0001c0001t0002g0216 |
3 | NA18947.hp1 NA19011.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.3631-116T>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461761 | |||||||
| chr17:30461856 | A | C | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0009g0023 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3631-21A>C | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 18/20 | chr17 | 30461856 | |||||||
| chr17:30462723 | A | G | 4 | a0001c0001t0007g0272 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916+254A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | chr17 | 30462723 | |||||||
| chr17:30462906 | TG | T | 12 | a0001c0001t0003g0011 a0001c0001t0003g0142 a0001c0001t0003g0143 others(9): Show |
13 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3916+440delG | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 30462906 | ||||||
| chr17:30463527 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3916+1058C>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | chr17 | 30463527 | |||||||
| chr17:30464101 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3917-487A>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | chr17 | 30464101 | |||||||
| chr17:30464126 | C | G | 1 | a0001c0001t0002g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3917-462C>G | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | chr17 | 30464126 | |||||||
| chr17:30464185 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3917-403G>A | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | chr17 | 30464185 | |||||||
| chr17:30464254 | G | T | 1 | a0001c0001t0005g0270 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3917-334G>T | CPD | ENSG00000108582.12 | transcript | ENST00000225719.9 | protein_coding | 20/20 | chr17 | 30464254 |