Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 324 |
| ensemblid | ENSG00000134982.18 |
| hgncid | 583 |
| symbol | APC |
| name | APC regulator of WNT signaling pathway |
| refseq_nuc | NM_000038.6 |
| refseq_prot | NP_000029.2 |
| ensembl_nuc | ENST00000257430.9 |
| ensembl_prot | ENSP00000257430.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 112737885 |
| end | 112846239 |
| strand | + |
| ver | v1.2 |
| region | chr5:112737885-112846239 |
| region5000 | chr5:112732885-112851239 |
| regionname0 | APC_chr5_112737885_112846239 |
| regionname5000 | APC_chr5_112732885_112851239 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2843 | 234 | 75 | 43 | 88 | 4 | 23 | 67 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0002 | 1/0 | 2843 | 42 | 3 | 11 | 18 | 2 | 7 | 17 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0003 | 0/0 | 2843 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0004 | 0/0 | 2842 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2837): Show |
chr5 | 112732885 | 112851239 |
| a0005 | 0/0 | 2843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0006 | 0/0 | 2843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0007 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0008 | 0/0 | 2843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0009 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0010 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0011 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0012 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0013 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| a0014 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | MAAAS others(2838): Show |
chr5 | 112732885 | 112851239 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 8529 | 96 | 5 | 26 | 47 | 2 | 15 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0002 | 0/0 | 8529 | 67 | 30 | 6 | 26 | 1 | 4 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0003 | 0/0 | 8529 | 44 | 20 | 8 | 13 | 1 | 2 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0005 | 0/0 | 8529 | 8 | 8 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0007 | 0/0 | 8529 | 3 | 1 | 2 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0008 | 0/0 | 8529 | 3 | 3 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0010 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0011 | 0/0 | 8529 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0014 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0015 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0016 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0019 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0026 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0027 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0029 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0030 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0001c0031 | 0/0 | 8529 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0002c0004 | 1/0 | 8529 | 40 | 2 | 11 | 17 | 2 | 7 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0002c0020 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0002c0025 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0003c0006 | 0/0 | 8529 | 3 | 1 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0004c0009 | 0/0 | 8526 | 3 | 2 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8521): Show |
chr5 | 112732885 | 112851239 | ||
| a0005c0013 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0006c0012 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0007c0023 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0008c0032 | 0/0 | 8529 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0009c0018 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0010c0017 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0011c0021 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0012c0022 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0013c0028 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 | ||
| a0014c0024 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ATGGC others(8524): Show |
chr5 | 112732885 | 112851239 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 10705 | 89 | 4 | 23 | 47 | 2 | 12 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0001t0004 | 0/0 | 10705 | 7 | 1 | 3 | 0 | 0 | 3 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0001 | 0/0 | 10705 | 4 | 0 | 0 | 4 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0003 | 0/0 | 10705 | 37 | 9 | 2 | 22 | 0 | 4 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0004 | 0/0 | 10705 | 16 | 13 | 3 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0005 | 0/0 | 10705 | 4 | 4 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0008 | 0/0 | 10705 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0009 | 0/0 | 10705 | 2 | 1 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0013 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0002t0015 | 0/0 | 10705 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0003t0002 | 0/0 | 10704 | 34 | 12 | 7 | 12 | 1 | 2 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0003t0006 | 0/0 | 10704 | 8 | 7 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0003t0010 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0003t0014 | 0/0 | 10704 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0005t0005 | 0/0 | 10705 | 7 | 7 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0005t0011 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0007t0004 | 0/0 | 10705 | 3 | 1 | 2 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0008t0002 | 0/0 | 10704 | 3 | 3 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0010t0007 | 0/0 | 10705 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0011t0002 | 0/0 | 10704 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0014t0007 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0015t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0016t0001 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0019t0002 | 0/0 | 10704 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0026t0006 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0027t0004 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0001c0029t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0030t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0001c0031t0002 | 0/0 | 10704 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0002c0004t0002 | 1/0 | 10704 | 40 | 2 | 11 | 17 | 2 | 7 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0002c0020t0012 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0002c0025t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0003c0006t0001 | 0/0 | 10705 | 3 | 1 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0004c0009t0002 | 0/0 | 10701 | 3 | 2 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10696): Show |
chr5 | 112732885 | 112851239 |
| a0005c0013t0002 | 0/0 | 10704 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0006c0012t0002 | 0/0 | 10704 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0007c0023t0004 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0008c0032t0002 | 0/0 | 10704 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0009c0018t0001 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0010c0017t0001 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0011c0021t0003 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0012c0022t0003 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| a0013c0028t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10699): Show |
chr5 | 112732885 | 112851239 |
| a0014c0024t0003 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | ACTGG others(10700): Show |
chr5 | 112732885 | 112851239 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0002t0015g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0003t0014g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0005t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0007t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0007t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0007t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0008t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0008t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0008t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0010t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0010t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0011t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0011t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0014t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0015t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0016t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0019t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0026t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0027t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0029t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0030t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0001c0031t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0020t0012g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0002c0025t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0003c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0003c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0003c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0004c0009t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0004c0009t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0004c0009t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0005c0013t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0005c0013t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0006c0012t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0006c0012t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0007c0023t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0008c0032t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0009c0018t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0010c0017t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0011c0021t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0012c0022t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0013c0028t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| a0014c0024t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0002 | t0015 | g0191 | EUR | FIN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00323 | hp2 | a0002 | c0004 | t0002 | g0016 | EUR | FIN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00408 | hp2 | a0002 | c0004 | t0002 | g0041 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00639 | hp2 | a0002 | c0004 | t0002 | g0086 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00733 | hp2 | a0002 | c0004 | t0002 | g0061 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG00741 | hp2 | a0001 | c0003 | t0006 | g0140 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01070 | hp1 | a0003 | c0006 | t0001 | g0263 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0188 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0189 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01081 | hp1 | a0001 | c0007 | t0004 | g0118 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01081 | hp2 | a0001 | c0031 | t0002 | g0073 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01099 | hp2 | a0002 | c0004 | t0002 | g0055 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0057 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01106 | hp2 | a0001 | c0007 | t0004 | g0119 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01109 | hp1 | a0002 | c0004 | t0002 | g0037 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0088 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01175 | hp2 | a0002 | c0004 | t0002 | g0036 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01243 | hp1 | a0004 | c0009 | t0002 | g0106 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01243 | hp2 | a0001 | c0002 | t0009 | g0131 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01256 | hp2 | a0002 | c0004 | t0002 | g0084 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01257 | hp1 | a0002 | c0004 | t0002 | g0034 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01258 | hp2 | a0002 | c0004 | t0002 | g0035 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0039 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0123 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01433 | hp1 | a0002 | c0004 | t0002 | g0070 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0137 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0138 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0053 | EUR | IBS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0134 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01891 | hp1 | a0001 | c0030 | t0002 | g0129 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0170 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01975 | hp1 | a0002 | c0004 | t0002 | g0072 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0190 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01993 | hp1 | a0002 | c0004 | t0002 | g0069 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02056 | hp1 | a0001 | c0019 | t0002 | g0079 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0043 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02145 | hp2 | a0001 | c0005 | t0005 | g0010 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0153 | EAS | CDX | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | CDX | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0128 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02258 | hp1 | a0001 | c0005 | t0011 | g0007 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02280 | hp1 | a0001 | c0005 | t0005 | g0009 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0151 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0060 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0169 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0032 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0178 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02523 | hp2 | a0001 | c0016 | t0001 | g0244 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02572 | hp1 | a0001 | c0003 | t0006 | g0142 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02572 | hp2 | a0004 | c0009 | t0002 | g0103 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02602 | hp2 | a0002 | c0004 | t0002 | g0013 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0030 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02615 | hp2 | a0001 | c0002 | t0008 | g0184 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02622 | hp1 | a0001 | c0003 | t0006 | g0144 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02622 | hp2 | a0001 | c0010 | t0007 | g0132 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02630 | hp1 | a0001 | c0015 | t0002 | g0135 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0145 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0157 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0092 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0159 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0019 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02717 | hp2 | a0001 | c0007 | t0004 | g0120 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02735 | hp1 | a0002 | c0004 | t0002 | g0038 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02818 | hp1 | a0001 | c0005 | t0005 | g0011 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0149 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02895 | hp1 | a0005 | c0013 | t0002 | g0148 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02895 | hp2 | a0001 | c0008 | t0002 | g0100 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02896 | hp1 | a0001 | c0003 | t0010 | g0139 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0126 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02897 | hp1 | a0005 | c0013 | t0002 | g0150 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0127 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02922 | hp1 | a0001 | c0008 | t0002 | g0104 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0152 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0179 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02965 | hp2 | a0001 | c0003 | t0002 | g0136 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0185 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02976 | hp2 | a0001 | c0005 | t0005 | g0006 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03098 | hp1 | a0007 | c0023 | t0004 | g0093 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0112 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03130 | hp1 | a0001 | c0026 | t0006 | g0143 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03130 | hp2 | a0001 | c0010 | t0007 | g0094 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0033 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0115 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0161 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0111 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03225 | hp1 | a0001 | c0003 | t0006 | g0147 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03225 | hp2 | a0001 | c0014 | t0007 | g0133 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03239 | hp2 | a0002 | c0004 | t0002 | g0083 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03453 | hp1 | a0006 | c0012 | t0002 | g0102 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0166 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03486 | hp2 | a0001 | c0008 | t0002 | g0130 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03490 | hp2 | a0001 | c0011 | t0002 | g0052 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03491 | hp1 | a0002 | c0004 | t0002 | g0062 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03492 | hp2 | a0001 | c0011 | t0002 | g0059 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03516 | hp1 | a0001 | c0002 | t0013 | g0003 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03516 | hp2 | a0001 | c0003 | t0006 | g0146 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0020 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03579 | hp2 | a0001 | c0003 | t0006 | g0141 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03654 | hp1 | a0002 | c0004 | t0002 | g0085 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0121 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0066 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0015 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0160 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03710 | hp2 | a0008 | c0032 | t0002 | g0017 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03927 | hp1 | a0003 | c0006 | t0001 | g0278 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG04115 | hp2 | a0002 | c0004 | t0002 | g0014 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG04184 | hp2 | a0002 | c0004 | t0002 | g0113 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18747 | hp1 | a0001 | c0003 | t0014 | g0049 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0067 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18953 | hp1 | a0002 | c0020 | t0012 | g0054 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0045 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18957 | hp1 | a0002 | c0004 | t0002 | g0099 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18963 | hp1 | a0002 | c0004 | t0002 | g0097 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18968 | hp2 | a0001 | c0003 | t0002 | g0044 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18970 | hp1 | a0002 | c0004 | t0002 | g0071 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18975 | hp1 | a0009 | c0018 | t0001 | g0284 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18975 | hp2 | a0002 | c0004 | t0002 | g0096 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18980 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18980 | hp2 | a0010 | c0017 | t0001 | g0197 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18985 | hp1 | a0002 | c0004 | t0002 | g0040 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18994 | hp1 | a0002 | c0004 | t0002 | g0078 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18998 | hp2 | a0002 | c0004 | t0002 | g0114 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19000 | hp1 | a0002 | c0004 | t0002 | g0087 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19006 | hp1 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19009 | hp2 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19010 | hp1 | a0002 | c0004 | t0002 | g0090 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0182 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19030 | hp2 | a0001 | c0005 | t0005 | g0008 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19058 | hp2 | a0002 | c0004 | t0002 | g0098 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19064 | hp2 | a0002 | c0004 | t0002 | g0089 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19065 | hp1 | a0011 | c0021 | t0003 | g0164 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19070 | hp2 | a0002 | c0004 | t0002 | g0095 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0080 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19082 | hp2 | a0002 | c0004 | t0002 | g0081 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19084 | hp1 | a0002 | c0004 | t0002 | g0077 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19085 | hp1 | a0012 | c0022 | t0003 | g0173 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0065 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19087 | hp2 | a0001 | c0003 | t0002 | g0192 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19091 | hp1 | a0002 | c0004 | t0002 | g0042 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19240 | hp1 | a0013 | c0028 | t0002 | g0105 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA20129 | hp1 | a0001 | c0002 | t0009 | g0125 | AFR | ASW | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA20129 | hp2 | a0001 | c0029 | t0002 | g0018 | AFR | ASW | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA20805 | hp1 | a0002 | c0004 | t0002 | g0063 | EUR | TSI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02109 | hp1 | a0002 | c0025 | t0002 | g0064 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02109 | hp2 | a0003 | c0006 | t0001 | g0277 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02486 | hp1 | a0001 | c0005 | t0005 | g0012 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02486 | hp2 | a0004 | c0009 | t0002 | g0107 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG02559 | hp2 | a0001 | c0005 | t0005 | g0005 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0058 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0177 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| HG06807 | hp2 | a0002 | c0004 | t0002 | g0082 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18955 | hp1 | a0002 | c0004 | t0002 | g0091 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA20300 | hp1 | a0002 | c0004 | t0002 | g0068 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA20300 | hp2 | a0001 | c0027 | t0004 | g0027 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA21309 | hp1 | a0006 | c0012 | t0002 | g0101 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| NA21309 | hp2 | a0014 | c0024 | t0003 | g0183 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0002 | g0109 | REF | REF | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:112827167 | A | G | 1 | a0005 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1468A>G | p.Asn490Asp | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/16 | 1527/10704 | 1468/8532 | 490/2843 | chr5 | 112827167 | |||
| chr5:112838180 | C | G | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2586C>G | p.Asn862Lys | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2645/10704 | 2586/8532 | 862/2843 | chr5 | 112838180 | |||
| chr5:112838202 | C | T | 1 | a0006 | 2 | HG03453.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2608C>T | p.Pro870Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2667/10704 | 2608/8532 | 870/2843 | chr5 | 112838202 | |||
| chr5:112838542 | T | C | 1 | a0011 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2948T>C | p.Ile983Thr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3007/10704 | 2948/8532 | 983/2843 | chr5 | 112838542 | |||
| chr5:112839053 | TGAA | T | 1 | a0004 | 3 | HG01243.hp1 HG02486.hp2 HG02572.hp2 |
disruptive_inframe_deletion | MODERATE | c.3468_3470delAGA | p.Glu1157del | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3527/10704 | 3468/8532 | 1156/2843 | INFO_REALIGN_3_PRIME | chr5 | 112839053 | ||
| chr5:112839244 | A | C | 1 | a0014 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3650A>C | p.Asn1217Thr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3709/10704 | 3650/8532 | 1217/2843 | chr5 | 112839244 | |||
| chr5:112839284 | G | C | 1 | a0012 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.3690G>C | p.Gln1230His | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3749/10704 | 3690/8532 | 1230/2843 | chr5 | 112839284 | |||
| chr5:112840212 | G | C | 1 | a0013 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.4618G>C | p.Glu1540Gln | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4677/10704 | 4618/8532 | 1540/2843 | chr5 | 112840212 | |||
| chr5:112840957 | G | A | 1 | a0010 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.5363G>A | p.Arg1788His | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5422/10704 | 5363/8532 | 1788/2843 | chr5 | 112840957 | |||
| chr5:112841059 | T | A | 12 | a0001 a0003 a0004 others(9): Show |
250 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(247): Show |
missense_variant | MODERATE | c.5465T>A | p.Val1822Asp | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5524/10704 | 5465/8532 | 1822/2843 | chr5 | 112841059 | |||
| chr5:112843098 | G | A | 1 | a0003 | 3 | HG01070.hp1 HG02109.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.7504G>A | p.Gly2502Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7563/10704 | 7504/8532 | 2502/2843 | chr5 | 112843098 | |||
| chr5:112843219 | A | G | 1 | a0007 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.7625A>G | p.Asn2542Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7684/10704 | 7625/8532 | 2542/2843 | chr5 | 112843219 | |||
| chr5:112843240 | G | A | 1 | a0009 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.7646G>A | p.Arg2549His | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7705/10704 | 7646/8532 | 2549/2843 | chr5 | 112843240 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:112755010 | G | A | 1 | a0001c0014 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.120G>A | p.Glu40Glu | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/16 | 179/10704 | 120/8532 | 40/2843 | chr5 | 112755010 | |||
| chr5:112827142 | G | A | 1 | a0001c0015 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1443G>A | p.Val481Val | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/16 | 1502/10704 | 1443/8532 | 481/2843 | chr5 | 112827142 | |||
| chr5:112827157 | T | C | 11 | a0001c0001 a0001c0005 a0001c0007 others(8): Show |
117 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(114): Show |
synonymous_variant | LOW | c.1458T>C | p.Tyr486Tyr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/16 | 1517/10704 | 1458/8532 | 486/2843 | chr5 | 112827157 | |||
| chr5:112828864 | G | A | 13 | a0001c0001 a0001c0002 a0001c0005 others(10): Show |
183 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(180): Show |
synonymous_variant | LOW | c.1635G>A | p.Ala545Ala | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/16 | 1694/10704 | 1635/8532 | 545/2843 | chr5 | 112828864 | |||
| chr5:112828924 | A | G | 1 | a0001c0005 | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.1695A>G | p.Glu565Glu | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/16 | 1754/10704 | 1695/8532 | 565/2843 | chr5 | 112828924 | |||
| chr5:112837553 | G | A | 1 | a0002c0025 | 1 | HG02109.hp1 | splice_region_variant&synonymous_variant | LOW | c.1959G>A | p.Arg653Arg | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2018/10704 | 1959/8532 | 653/2843 | chr5 | 112837553 | |||
| chr5:112838234 | C | T | 1 | a0001c0031 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.2640C>T | p.Ile880Ile | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2699/10704 | 2640/8532 | 880/2843 | chr5 | 112838234 | |||
| chr5:112838759 | A | T | 1 | a0001c0011 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.3165A>T | p.Ile1055Ile | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3224/10704 | 3165/8532 | 1055/2843 | chr5 | 112838759 | |||
| chr5:112838858 | G | A | 1 | a0001c0026 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.3264G>A | p.Lys1088Lys | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3323/10704 | 3264/8532 | 1088/2843 | chr5 | 112838858 | |||
| chr5:112839326 | A | G | 1 | a0001c0005 | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.3732A>G | p.Gln1244Gln | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3791/10704 | 3732/8532 | 1244/2843 | chr5 | 112839326 | |||
| chr5:112839959 | T | C | 1 | a0001c0016 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.4365T>C | p.Asn1455Asn | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4424/10704 | 4365/8532 | 1455/2843 | chr5 | 112839959 | |||
| chr5:112840073 | G | A | 14 | a0001c0001 a0001c0002 a0001c0005 others(11): Show |
184 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(181): Show |
synonymous_variant | LOW | c.4479G>A | p.Thr1493Thr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4538/10704 | 4479/8532 | 1493/2843 | chr5 | 112840073 | |||
| chr5:112840379 | C | G | 1 | a0002c0020 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.4785C>G | p.Ala1595Ala | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4844/10704 | 4785/8532 | 1595/2843 | chr5 | 112840379 | |||
| chr5:112840628 | G | A | 15 | a0001c0001 a0001c0002 a0001c0005 others(12): Show |
185 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(182): Show |
synonymous_variant | LOW | c.5034G>A | p.Gly1678Gly | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5093/10704 | 5034/8532 | 1678/2843 | chr5 | 112840628 | |||
| chr5:112840844 | C | G | 2 | a0001c0010 a0001c0014 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.5250C>G | p.Val1750Val | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5309/10704 | 5250/8532 | 1750/2843 | chr5 | 112840844 | |||
| chr5:112840862 | T | G | 15 | a0001c0001 a0001c0002 a0001c0005 others(12): Show |
185 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(182): Show |
synonymous_variant | LOW | c.5268T>G | p.Ser1756Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5327/10704 | 5268/8532 | 1756/2843 | chr5 | 112840862 | |||
| chr5:112841474 | G | A | 14 | a0001c0001 a0001c0002 a0001c0005 others(11): Show |
184 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(181): Show |
synonymous_variant | LOW | c.5880G>A | p.Pro1960Pro | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5939/10704 | 5880/8532 | 1960/2843 | chr5 | 112841474 | |||
| chr5:112842788 | C | T | 1 | a0001c0030 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.7194C>T | p.Ser2398Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7253/10704 | 7194/8532 | 2398/2843 | chr5 | 112842788 | |||
| chr5:112842795 | C | T | 1 | a0001c0007 | 3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.7201C>T | p.Leu2401Leu | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7260/10704 | 7201/8532 | 2401/2843 | chr5 | 112842795 | |||
| chr5:112843298 | A | G | 5 | a0001c0008 a0001c0030 a0004c0009 others(2): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.7704A>G | p.Gly2568Gly | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7763/10704 | 7704/8532 | 2568/2843 | chr5 | 112843298 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:112844212 | C | A | 7 | a0001c0002t0003 a0001c0003t0006 a0001c0003t0010 others(4): Show |
50 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*86C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 86 | chr5 | 112844212 | ||||||
| chr5:112844374 | A | G | 1 | a0001c0002t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 248 | chr5 | 112844374 | ||||||
| chr5:112844531 | C | CA | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0002t0001 others(22): Show |
188 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*414dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 415 | INFO_REALIGN_3_PRIME | chr5 | 112844531 | |||||
| chr5:112844560 | C | T | 6 | a0001c0002t0003 a0001c0003t0006 a0001c0026t0006 others(3): Show |
49 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 434 | chr5 | 112844560 | ||||||
| chr5:112844635 | C | A | 1 | a0001c0003t0014 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 509 | chr5 | 112844635 | ||||||
| chr5:112844781 | G | T | 1 | a0001c0002t0009 | 2 | HG01243.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 655 | chr5 | 112844781 | ||||||
| chr5:112845176 | T | C | 3 | a0001c0002t0005 a0001c0005t0005 a0001c0005t0011 |
12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1050T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1050 | chr5 | 112845176 | ||||||
| chr5:112845224 | T | C | 7 | a0001c0001t0001 a0001c0002t0001 a0001c0016t0001 others(4): Show |
99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1098 | chr5 | 112845224 | ||||||
| chr5:112845314 | C | G | 1 | a0001c0005t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1188C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1188 | chr5 | 112845314 | ||||||
| chr5:112845329 | A | C | 1 | a0001c0002t0008 | 2 | HG02615.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1203A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1203 | chr5 | 112845329 | ||||||
| chr5:112845430 | G | A | 1 | a0001c0002t0013 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1304G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1304 | chr5 | 112845430 | ||||||
| chr5:112845586 | C | T | 6 | a0001c0002t0003 a0001c0003t0006 a0001c0026t0006 others(3): Show |
49 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1460C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1460 | chr5 | 112845586 | ||||||
| chr5:112845682 | C | G | 9 | a0001c0001t0001 a0001c0002t0001 a0001c0010t0007 others(6): Show |
102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1556C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1556 | chr5 | 112845682 | ||||||
| chr5:112845879 | G | A | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0002t0001 others(23): Show |
196 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1753G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1753 | chr5 | 112845879 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:112737970 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+45G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112737970 | |||||||
| chr5:112737978 | T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+53T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112737978 | |||||||
| chr5:112738420 | T | C | 1 | a0001c0003t0002g0004 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-19+495T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738420 | |||||||
| chr5:112738564 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+639G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738564 | |||||||
| chr5:112738572 | A | G | 100 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19+647A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738572 | |||||||
| chr5:112738659 | C | T | 162 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(159): Show |
164 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(161): Show |
intron_variant | MODIFIER | c.-19+734C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738659 | |||||||
| chr5:112738768 | T | A | 2 | a0001c0010t0007g0132 a0001c0014t0007g0133 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+843T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738768 | |||||||
| chr5:112738890 | A | G | 1 | a0001c0002t0009g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19+965A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738890 | |||||||
| chr5:112738893 | C | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+968C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738893 | |||||||
| chr5:112738910 | A | G | 2 | a0001c0008t0002g0130 a0001c0030t0002g0129 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-19+985A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738910 | |||||||
| chr5:112739025 | C | G | 100 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19+1100C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739025 | |||||||
| chr5:112739072 | A | G | 2 | a0001c0002t0003g0186 a0001c0002t0003g0187 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-19+1147A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739072 | |||||||
| chr5:112739271 | C | G | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+1346C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739271 | |||||||
| chr5:112739299 | G | T | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+1374G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739299 | |||||||
| chr5:112739447 | C | T | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19+1522C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739447 | |||||||
| chr5:112739492 | C | G | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-19+1567C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739492 | |||||||
| chr5:112739662 | C | T | 1 | a0014c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+1737C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739662 | |||||||
| chr5:112739788 | C | T | 10 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(7): Show |
10 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+1863C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739788 | |||||||
| chr5:112739888 | T | C | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+1963T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739888 | |||||||
| chr5:112740067 | CAG | C | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19+2145_-19+2146d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112740067 | ||||||
| chr5:112740081 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+2156A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740081 | |||||||
| chr5:112740159 | A | G | 1 | a0002c0004t0002g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-19+2234A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740159 | |||||||
| chr5:112740250 | T | C | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19+2325T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740250 | |||||||
| chr5:112740503 | T | C | 1 | a0001c0015t0002g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19+2578T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740503 | |||||||
| chr5:112740523 | TC | T | 9 | a0001c0001t0001g0122 a0001c0001t0004g0117 a0001c0001t0004g0121 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+2599delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740523 | |||||||
| chr5:112740524 | C | CT | 10 | a0001c0001t0001g0075 a0001c0002t0003g0076 a0001c0002t0004g0188 others(7): Show |
10 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+2618dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112740524 | ||||||
| chr5:112740524 | C | T | 39 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(36): Show |
41 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-19+2599C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740524 | |||||||
| chr5:112740524 | CT | C | 121 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(118): Show |
121 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.-19+2618delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112740524 | ||||||
| chr5:112740525 | T | C | 38 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(35): Show |
40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19+2600T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740525 | |||||||
| chr5:112740526 | T | C | 9 | a0001c0001t0001g0122 a0001c0001t0004g0117 a0001c0001t0004g0121 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+2601T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740526 | |||||||
| chr5:112740547 | A | G | 1 | a0002c0004t0002g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+2622A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740547 | |||||||
| chr5:112740580 | G | A | 2 | a0002c0004t0002g0013 a0002c0004t0002g0014 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-19+2655G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740580 | |||||||
| chr5:112740594 | G | A | 19 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(16): Show |
19 | HG00741.hp2 HG01496.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+2669G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740594 | |||||||
| chr5:112740645 | C | T | 1 | a0001c0005t0005g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+2720C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740645 | |||||||
| chr5:112740704 | T | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+2779T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740704 | |||||||
| chr5:112740752 | G | C | 286 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(283): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-19+2827G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740752 | |||||||
| chr5:112740856 | T | C | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2931T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740856 | |||||||
| chr5:112740907 | A | C | 1 | a0001c0003t0006g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19+2982A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740907 | |||||||
| chr5:112740924 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-19+2999T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740924 | |||||||
| chr5:112741124 | TATC | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | NA18953.hp2 NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-19+3203_-19+3205d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112741124 | ||||||
| chr5:112741182 | C | T | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+3257C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741182 | |||||||
| chr5:112741560 | T | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+3635T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741560 | |||||||
| chr5:112741600 | A | T | 1 | a0001c0003t0002g0137 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-19+3675A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741600 | |||||||
| chr5:112741620 | A | C | 5 | a0002c0004t0002g0095 a0002c0004t0002g0096 a0002c0004t0002g0097 others(2): Show |
5 | NA18957.hp1 NA18963.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+3695A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741620 | |||||||
| chr5:112741652 | T | C | 1 | a0010c0017t0001g0197 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-19+3727T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741652 | |||||||
| chr5:112741750 | T | A | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.-19+3825T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741750 | |||||||
| chr5:112741759 | A | G | 2 | a0001c0002t0003g0186 a0001c0002t0003g0187 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-19+3834A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741759 | |||||||
| chr5:112741983 | T | C | 3 | a0001c0003t0002g0015 a0002c0004t0002g0016 a0008c0032t0002g0017 |
3 | HG00323.hp2 HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-19+4058T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741983 | |||||||
| chr5:112741984 | C | T | 58 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(55): Show |
60 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19+4059C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741984 | |||||||
| chr5:112741991 | A | G | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4066A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741991 | |||||||
| chr5:112742073 | A | G | 170 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(167): Show |
172 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(169): Show |
intron_variant | MODIFIER | c.-19+4148A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742073 | |||||||
| chr5:112742082 | G | A | 16 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(13): Show |
16 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4157G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742082 | |||||||
| chr5:112742106 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-19+4181G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742106 | |||||||
| chr5:112742223 | G | C | 103 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(100): Show |
103 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.-19+4298G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742223 | |||||||
| chr5:112742398 | C | T | 1 | a0009c0018t0001g0284 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-19+4473C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742398 | |||||||
| chr5:112742896 | G | A | 3 | a0001c0002t0003g0153 a0001c0002t0003g0154 a0001c0002t0003g0155 |
3 | HG02155.hp1 NA18990.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-19+4971G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742896 | |||||||
| chr5:112742955 | C | G | 1 | a0001c0001t0001g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19+5030C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742955 | |||||||
| chr5:112743054 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-19+5129C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743054 | |||||||
| chr5:112743085 | A | G | 5 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0121 others(2): Show |
5 | HG01358.hp1 HG01361.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+5160A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743085 | |||||||
| chr5:112743129 | CCT | C | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+5207_-19+5208d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112743129 | ||||||
| chr5:112743174 | T | C | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+5249T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743174 | |||||||
| chr5:112743234 | T | C | 3 | a0002c0004t0002g0034 a0002c0004t0002g0035 a0002c0004t0002g0036 |
3 | HG01175.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-19+5309T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743234 | |||||||
| chr5:112743420 | AT | A | 157 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(154): Show |
159 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.-19+5503delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112743420 | ||||||
| chr5:112743470 | T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+5545T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743470 | |||||||
| chr5:112743510 | A | G | 15 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(12): Show |
15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+5585A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743510 | |||||||
| chr5:112743906 | C | T | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-19+5981C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743906 | |||||||
| chr5:112744160 | T | C | 10 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(7): Show |
10 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+6235T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744160 | |||||||
| chr5:112744178 | A | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+6253A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744178 | |||||||
| chr5:112744185 | T | G | 100 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19+6260T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744185 | |||||||
| chr5:112744582 | A | G | 9 | a0001c0002t0013g0003 a0001c0005t0005g0005 a0001c0005t0005g0006 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+6657A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744582 | |||||||
| chr5:112744600 | A | G | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19+6675A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744600 | |||||||
| chr5:112744697 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-19+6772T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744697 | |||||||
| chr5:112744815 | T | G | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-19+6890T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744815 | |||||||
| chr5:112744993 | G | A | 10 | a0001c0003t0006g0140 a0001c0003t0006g0141 a0001c0003t0006g0142 others(7): Show |
10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+7068G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744993 | |||||||
| chr5:112745031 | G | A | 71 | a0001c0001t0001g0075 a0001c0002t0003g0074 a0001c0002t0003g0076 others(68): Show |
71 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19+7106G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745031 | |||||||
| chr5:112745059 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+7134T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745059 | |||||||
| chr5:112745130 | G | GTA | 166 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(163): Show |
168 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(165): Show |
intron_variant | MODIFIER | c.-19+7205_-19+7206i others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745130 | |||||||
| chr5:112745205 | A | G | 1 | a0002c0004t0002g0091 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-19+7280A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745205 | |||||||
| chr5:112745341 | A | G | 15 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(12): Show |
15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+7416A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745341 | |||||||
| chr5:112745548 | T | TTTA | 98 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-19+7650_-19+7652d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | ||||||
| chr5:112745548 | T | TTTATTA | 10 | a0001c0001t0001g0199 a0001c0003t0002g0149 a0001c0010t0007g0094 others(7): Show |
10 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+7647_-19+7652d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | ||||||
| chr5:112745548 | TTTA | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+7650_-19+7652d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | ||||||
| chr5:112745548 | TTTATTA | T | 4 | a0001c0001t0001g0279 a0001c0002t0008g0184 a0001c0002t0008g0185 others(1): Show |
4 | HG01346.hp2 HG02615.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+7647_-19+7652d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | ||||||
| chr5:112745548 | TTTATTAT others(2): Show |
T | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0003g0179 |
3 | HG02965.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-19+7644_-19+7652d others(11): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | ||||||
| chr5:112745565 | T | C | 1 | a0002c0004t0002g0037 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+7640T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745565 | |||||||
| chr5:112745575 | A | T | 1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+7650A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745575 | |||||||
| chr5:112745644 | A | G | 13 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(10): Show |
13 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+7719A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745644 | |||||||
| chr5:112745670 | CT | C | 15 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(12): Show |
15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+7747delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745670 | ||||||
| chr5:112745679 | C | G | 2 | a0001c0003t0002g0032 a0001c0003t0002g0033 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-19+7754C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745679 | |||||||
| chr5:112745682 | C | A | 79 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(76): Show |
79 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.-19+7757C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745682 | |||||||
| chr5:112745725 | G | A | 2 | a0001c0003t0002g0032 a0001c0003t0002g0033 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-19+7800G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745725 | |||||||
| chr5:112745815 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-19+7890A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745815 | |||||||
| chr5:112746136 | GGAAA | G | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19+8216_-19+8219d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112746136 | ||||||
| chr5:112746227 | A | G | 100 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19+8302A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746227 | |||||||
| chr5:112746307 | G | T | 1 | a0002c0004t0002g0037 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+8382G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746307 | |||||||
| chr5:112746449 | T | A | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-8424T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746449 | |||||||
| chr5:112746476 | T | C | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-8397T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746476 | |||||||
| chr5:112746951 | TTA | T | 97 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(94): Show |
97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.-18-7920_-18-7919d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112746951 | ||||||
| chr5:112747122 | C | T | 1 | a0001c0002t0003g0178 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-18-7751C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747122 | |||||||
| chr5:112747192 | A | G | 2 | a0003c0006t0001g0277 a0003c0006t0001g0278 |
2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-18-7681A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747192 | |||||||
| chr5:112747241 | A | AG | 184 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(181): Show |
186 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(183): Show |
intron_variant | MODIFIER | c.-18-7626dupG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112747241 | ||||||
| chr5:112747387 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-18-7486G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747387 | |||||||
| chr5:112747598 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-18-7275C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747598 | |||||||
| chr5:112747607 | C | T | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-18-7266C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747607 | |||||||
| chr5:112747643 | A | G | 1 | a0004c0009t0002g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-7230A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747643 | |||||||
| chr5:112747672 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-18-7201G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747672 | |||||||
| chr5:112747720 | A | G | 15 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(12): Show |
15 | HG01981.hp1 HG01993.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-7153A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747720 | |||||||
| chr5:112747761 | A | G | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18-7112A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747761 | |||||||
| chr5:112747844 | A | G | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18-7029A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747844 | |||||||
| chr5:112747862 | A | G | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-18-7011A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747862 | |||||||
| chr5:112747956 | T | C | 1 | a0001c0003t0002g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18-6917T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747956 | |||||||
| chr5:112748072 | A | G | 1 | a0001c0002t0015g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18-6801A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748072 | |||||||
| chr5:112748109 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-18-6764G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748109 | |||||||
| chr5:112748148 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-6725C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748148 | |||||||
| chr5:112748205 | A | T | 1 | a0001c0003t0002g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18-6668A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748205 | |||||||
| chr5:112748259 | A | G | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-6614A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748259 | |||||||
| chr5:112748329 | A | T | 2 | a0001c0003t0006g0146 a0001c0003t0006g0147 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-18-6544A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748329 | |||||||
| chr5:112748343 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-6530G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748343 | |||||||
| chr5:112748392 | G | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-6481G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748392 | |||||||
| chr5:112748599 | C | T | 3 | a0001c0002t0003g0176 a0001c0002t0003g0177 a0001c0002t0003g0182 |
3 | HG03471.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-6274C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748599 | |||||||
| chr5:112748855 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-18-6018G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748855 | |||||||
| chr5:112749046 | G | T | 1 | a0008c0032t0002g0017 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-5827G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749046 | |||||||
| chr5:112749132 | G | A | 1 | a0001c0003t0002g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18-5741G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749132 | |||||||
| chr5:112749138 | C | G | 1 | a0001c0003t0002g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-18-5735C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749138 | |||||||
| chr5:112749194 | C | T | 1 | a0002c0004t0002g0016 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-18-5679C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749194 | |||||||
| chr5:112749311 | A | T | 1 | a0007c0023t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18-5562A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749311 | |||||||
| chr5:112749373 | A | G | 1 | a0002c0004t0002g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-18-5500A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749373 | |||||||
| chr5:112749479 | A | AT | 110 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(107): Show |
110 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.-18-5371dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749479 | ||||||
| chr5:112749479 | A | ATT | 31 | a0001c0001t0001g0200 a0001c0001t0001g0241 a0001c0001t0001g0242 others(28): Show |
31 | HG00639.hp2 HG00673.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-5372_-18-5371d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749479 | ||||||
| chr5:112749479 | A | ATTT | 29 | a0001c0001t0001g0259 a0001c0002t0003g0001 a0001c0002t0003g0002 others(26): Show |
31 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18-5373_-18-5371d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749479 | ||||||
| chr5:112749502 | TG | T | 13 | a0001c0003t0002g0138 a0001c0003t0006g0140 a0001c0003t0006g0141 others(10): Show |
13 | HG00741.hp2 HG01496.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-5370delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749502 | |||||||
| chr5:112749510 | A | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-5363A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749510 | |||||||
| chr5:112749517 | C | T | 4 | a0001c0002t0003g0174 a0001c0002t0003g0175 a0001c0002t0003g0178 others(1): Show |
4 | HG00609.hp1 HG02523.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-5356C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749517 | |||||||
| chr5:112749564 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-18-5309A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749564 | |||||||
| chr5:112749590 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-18-5283C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749590 | |||||||
| chr5:112749623 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-5250G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749623 | |||||||
| chr5:112749648 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-18-5225C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749648 | |||||||
| chr5:112749662 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18-5211A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749662 | |||||||
| chr5:112749676 | C | T | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-5197C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749676 | |||||||
| chr5:112749740 | C | G | 21 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(18): Show |
21 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-5133C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749740 | |||||||
| chr5:112749776 | C | T | 1 | a0001c0002t0003g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-18-5097C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749776 | |||||||
| chr5:112749803 | A | G | 40 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(37): Show |
42 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-18-5070A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749803 | |||||||
| chr5:112749914 | T | G | 100 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-18-4959T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749914 | |||||||
| chr5:112749932 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG02071.hp2 HG02132.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-4941A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749932 | |||||||
| chr5:112749968 | G | GT | 25 | a0001c0001t0001g0200 a0001c0001t0001g0248 a0001c0001t0001g0249 others(22): Show |
25 | HG00642.hp1 HG00673.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-4893dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749968 | ||||||
| chr5:112749968 | G | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-4905G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749968 | |||||||
| chr5:112750023 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18-4850C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750023 | |||||||
| chr5:112750025 | C | T | 2 | a0001c0002t0003g0186 a0001c0002t0003g0187 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-18-4848C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750025 | |||||||
| chr5:112750032 | G | A | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-4841G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750032 | |||||||
| chr5:112750218 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-4655C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750218 | |||||||
| chr5:112750353 | C | T | 2 | a0001c0008t0002g0130 a0001c0030t0002g0129 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-18-4520C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750353 | |||||||
| chr5:112750468 | T | A | 98 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-18-4405T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750468 | |||||||
| chr5:112750488 | A | ATGTT | 98 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-18-4375_-18-4372d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112750488 | ||||||
| chr5:112750679 | C | A | 1 | a0002c0004t0002g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-18-4194C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750679 | |||||||
| chr5:112750700 | A | G | 1 | a0002c0004t0002g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-18-4173A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750700 | |||||||
| chr5:112751005 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-18-3868C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751005 | |||||||
| chr5:112751050 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-3823C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751050 | |||||||
| chr5:112751067 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18-3806T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751067 | |||||||
| chr5:112751177 | C | T | 54 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(51): Show |
56 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18-3696C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751177 | |||||||
| chr5:112751228 | AC | A | 3 | a0001c0002t0003g0169 a0001c0002t0003g0170 a0001c0002t0003g0171 |
3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-18-3644delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751228 | |||||||
| chr5:112751249 | A | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-3624A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751249 | |||||||
| chr5:112751293 | A | G | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-18-3580A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751293 | |||||||
| chr5:112751343 | A | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-3530A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751343 | |||||||
| chr5:112751416 | TAA | T | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-3456_-18-3455d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751416 | |||||||
| chr5:112751478 | A | C | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3395A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751478 | |||||||
| chr5:112751523 | T | C | 1 | a0001c0002t0003g0162 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-3350T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751523 | |||||||
| chr5:112751630 | T | G | 171 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(168): Show |
173 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(170): Show |
intron_variant | MODIFIER | c.-18-3243T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751630 | |||||||
| chr5:112751684 | A | T | 4 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0001g0275 others(1): Show |
4 | HG00741.hp1 HG01109.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3189A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751684 | |||||||
| chr5:112751808 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18-3065A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751808 | |||||||
| chr5:112752015 | T | C | 48 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(45): Show |
50 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-2858T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752015 | |||||||
| chr5:112752803 | C | T | 2 | a0002c0004t0002g0016 a0008c0032t0002g0017 |
2 | HG00323.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-18-2070C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752803 | |||||||
| chr5:112752810 | G | A | 286 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(283): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-18-2063G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752810 | |||||||
| chr5:112752907 | T | C | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-1966T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752907 | |||||||
| chr5:112752907 | T | G | 37 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(34): Show |
39 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18-1966T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752907 | |||||||
| chr5:112752948 | C | T | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-1925C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752948 | |||||||
| chr5:112752969 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-1904G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752969 | |||||||
| chr5:112753564 | A | T | 1 | a0001c0005t0005g0009 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-1309A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753564 | |||||||
| chr5:112753585 | T | C | 96 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(93): Show |
96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.-18-1288T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753585 | |||||||
| chr5:112753667 | G | A | 2 | a0001c0003t0002g0138 a0001c0003t0002g0151 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-18-1206G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753667 | |||||||
| chr5:112753747 | C | T | 1 | a0003c0006t0001g0263 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-18-1126C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753747 | |||||||
| chr5:112753748 | G | A | 1 | a0001c0003t0002g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-18-1125G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753748 | |||||||
| chr5:112753783 | T | C | 202 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(199): Show |
204 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(201): Show |
intron_variant | MODIFIER | c.-18-1090T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753783 | |||||||
| chr5:112753847 | A | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18-1026A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753847 | |||||||
| chr5:112753865 | C | G | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-1008C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753865 | |||||||
| chr5:112754002 | T | C | 2 | a0001c0002t0004g0188 a0001c0002t0004g0189 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18-871T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754002 | |||||||
| chr5:112754116 | T | C | 10 | a0001c0003t0006g0140 a0001c0003t0006g0141 a0001c0003t0006g0142 others(7): Show |
10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-757T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754116 | |||||||
| chr5:112754239 | A | G | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-18-634A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754239 | |||||||
| chr5:112754258 | A | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-615A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754258 | |||||||
| chr5:112754312 | C | A | 2 | a0002c0004t0002g0077 a0002c0004t0002g0091 |
2 | NA18955.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-18-561C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754312 | |||||||
| chr5:112755248 | T | G | 4 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+223T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112755248 | |||||||
| chr5:112755707 | C | T | 1 | a0001c0003t0002g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.135+682C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112755707 | |||||||
| chr5:112755944 | C | CA | 21 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0242 others(18): Show |
21 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+934dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112755944 | ||||||
| chr5:112755944 | CA | C | 8 | a0001c0001t0001g0276 a0001c0002t0003g0171 a0001c0002t0008g0185 others(5): Show |
8 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+934delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112755944 | ||||||
| chr5:112756007 | C | G | 167 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(164): Show |
169 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(166): Show |
intron_variant | MODIFIER | c.135+982C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756007 | |||||||
| chr5:112756013 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.135+988T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756013 | |||||||
| chr5:112756276 | C | T | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.135+1251C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756276 | |||||||
| chr5:112756358 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.135+1333A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756358 | |||||||
| chr5:112756367 | CATTTT | C | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+1346_135+1350d others(7): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112756367 | ||||||
| chr5:112756481 | A | T | 1 | a0001c0002t0003g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.135+1456A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756481 | |||||||
| chr5:112756619 | G | A | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+1594G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756619 | |||||||
| chr5:112756672 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.135+1647A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756672 | |||||||
| chr5:112756705 | T | G | 102 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(99): Show |
102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.135+1680T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756705 | |||||||
| chr5:112756801 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.135+1776A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756801 | |||||||
| chr5:112756803 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+1778A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756803 | |||||||
| chr5:112756928 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+1903G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756928 | |||||||
| chr5:112757185 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.135+2160A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757185 | |||||||
| chr5:112757259 | A | G | 1 | a0001c0002t0003g0002 | 2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.135+2234A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757259 | |||||||
| chr5:112757335 | A | C | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.135+2310A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757335 | |||||||
| chr5:112757353 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+2328T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757353 | |||||||
| chr5:112757407 | G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.135+2382G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757407 | |||||||
| chr5:112757411 | C | G | 2 | a0001c0002t0003g0186 a0001c0002t0003g0187 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.135+2386C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757411 | |||||||
| chr5:112757728 | G | C | 1 | a0002c0004t0002g0041 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.135+2703G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757728 | |||||||
| chr5:112757874 | C | T | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.135+2849C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757874 | |||||||
| chr5:112757876 | C | T | 5 | a0002c0004t0002g0095 a0002c0004t0002g0096 a0002c0004t0002g0097 others(2): Show |
5 | NA18957.hp1 NA18963.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+2851C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757876 | |||||||
| chr5:112758182 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+3157T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758182 | |||||||
| chr5:112758251 | G | A | 3 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0078 |
3 | HG00408.hp2 NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.135+3226G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758251 | |||||||
| chr5:112758258 | A | G | 286 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(283): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.135+3233A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758258 | |||||||
| chr5:112758305 | T | TTTTG | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+3292_135+3295d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112758305 | ||||||
| chr5:112758313 | GTTTGTTT | G | 101 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(98): Show |
101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.135+3311_135+3317d others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112758313 | ||||||
| chr5:112758412 | C | T | 6 | a0002c0004t0002g0068 a0002c0004t0002g0069 a0002c0004t0002g0070 others(3): Show |
6 | HG01433.hp1 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+3387C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758412 | |||||||
| chr5:112758430 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.135+3405G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758430 | |||||||
| chr5:112758515 | C | T | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3490C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758515 | |||||||
| chr5:112758638 | T | A | 2 | a0001c0001t0004g0121 a0001c0001t0004g0124 |
2 | HG01358.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.135+3613T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758638 | |||||||
| chr5:112758647 | A | G | 1 | a0001c0003t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.135+3622A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758647 | |||||||
| chr5:112758707 | G | A | 165 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(162): Show |
167 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.135+3682G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758707 | |||||||
| chr5:112758755 | C | T | 1 | a0001c0005t0005g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135+3730C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758755 | |||||||
| chr5:112758757 | C | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3732C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758757 | |||||||
| chr5:112758919 | A | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG00642.hp2 HG01074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.135+3894A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758919 | |||||||
| chr5:112759036 | C | T | 1 | a0002c0004t0002g0085 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.135+4011C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759036 | |||||||
| chr5:112759139 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+4114C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759139 | |||||||
| chr5:112759245 | G | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+4220G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759245 | |||||||
| chr5:112759335 | A | G | 2 | a0001c0002t0003g0168 a0001c0002t0003g0180 |
2 | NA18974.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.135+4310A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759335 | |||||||
| chr5:112759356 | C | CT | 72 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0242 others(69): Show |
74 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.135+4351dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112759356 | ||||||
| chr5:112759356 | CT | C | 8 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0205 others(5): Show |
8 | HG01169.hp1 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+4351delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112759356 | ||||||
| chr5:112759360 | T | C | 15 | a0001c0003t0002g0004 a0001c0003t0002g0032 a0001c0003t0002g0043 others(12): Show |
15 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+4335T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759360 | |||||||
| chr5:112759385 | G | A | 1 | a0001c0003t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.135+4360G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759385 | |||||||
| chr5:112759443 | C | T | 96 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(93): Show |
96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.135+4418C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759443 | |||||||
| chr5:112759444 | G | A | 1 | a0002c0004t0002g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.135+4419G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759444 | |||||||
| chr5:112759451 | G | A | 15 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(12): Show |
15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+4426G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759451 | |||||||
| chr5:112759502 | C | T | 1 | a0002c0004t0002g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.135+4477C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759502 | |||||||
| chr5:112759566 | C | G | 1 | a0002c0004t0002g0037 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+4541C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759566 | |||||||
| chr5:112759635 | G | A | 56 | a0001c0001t0001g0075 a0001c0002t0003g0074 a0001c0002t0003g0076 others(53): Show |
56 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.135+4610G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759635 | |||||||
| chr5:112759672 | A | T | 2 | a0001c0002t0003g0159 a0001c0002t0003g0160 |
2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.135+4647A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759672 | |||||||
| chr5:112759796 | T | C | 1 | a0001c0002t0003g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.135+4771T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759796 | |||||||
| chr5:112760078 | T | A | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.135+5053T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760078 | |||||||
| chr5:112760171 | A | G | 1 | a0001c0002t0003g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.135+5146A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760171 | |||||||
| chr5:112760255 | G | A | 1 | a0002c0004t0002g0081 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.135+5230G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760255 | |||||||
| chr5:112760570 | C | A | 1 | a0002c0004t0002g0091 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.135+5545C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760570 | |||||||
| chr5:112760679 | G | C | 1 | a0001c0002t0003g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.136-5647G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760679 | |||||||
| chr5:112760812 | AT | A | 11 | a0001c0001t0001g0075 a0001c0008t0002g0100 a0001c0008t0002g0104 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-5500delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112760812 | ||||||
| chr5:112760929 | C | T | 98 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.136-5397C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760929 | |||||||
| chr5:112760968 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.136-5358C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760968 | |||||||
| chr5:112760973 | C | A | 8 | a0001c0002t0004g0022 a0001c0002t0004g0023 a0001c0002t0004g0024 others(5): Show |
8 | HG02258.hp2 HG02559.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5353C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760973 | |||||||
| chr5:112761014 | T | C | 2 | a0006c0012t0002g0101 a0006c0012t0002g0102 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.136-5312T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761014 | |||||||
| chr5:112761020 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.136-5306A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761020 | |||||||
| chr5:112761045 | G | A | 1 | a0001c0003t0002g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.136-5281G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761045 | |||||||
| chr5:112761089 | G | A | 1 | a0001c0002t0003g0159 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.136-5237G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761089 | |||||||
| chr5:112761108 | G | A | 1 | a0002c0025t0002g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.136-5218G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761108 | |||||||
| chr5:112761507 | C | T | 2 | a0001c0003t0002g0138 a0001c0003t0002g0151 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.136-4819C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761507 | |||||||
| chr5:112761534 | C | G | 1 | a0001c0001t0004g0116 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.136-4792C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761534 | |||||||
| chr5:112761537 | G | A | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.136-4789G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761537 | |||||||
| chr5:112761558 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-4768A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761558 | |||||||
| chr5:112761792 | A | G | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4534A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761792 | |||||||
| chr5:112761819 | A | G | 1 | a0001c0002t0003g0156 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.136-4507A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761819 | |||||||
| chr5:112761859 | A | C | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.136-4467A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761859 | |||||||
| chr5:112761996 | CAGTTCAG others(4): Show |
C | 1 | a0007c0023t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.136-4329_136-4319d others(13): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761996 | |||||||
| chr5:112762060 | A | G | 109 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(106): Show |
109 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.136-4266A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762060 | |||||||
| chr5:112762073 | T | TA | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.136-4249dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112762073 | ||||||
| chr5:112762313 | A | G | 1 | a0001c0003t0002g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.136-4013A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762313 | |||||||
| chr5:112762398 | A | G | 4 | a0001c0001t0001g0122 a0001c0001t0004g0121 a0001c0001t0004g0123 others(1): Show |
4 | HG01358.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-3928A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762398 | |||||||
| chr5:112762399 | C | T | 1 | a0001c0002t0009g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136-3927C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762399 | |||||||
| chr5:112762406 | A | G | 1 | a0002c0004t0002g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.136-3920A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762406 | |||||||
| chr5:112762630 | C | T | 14 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(11): Show |
14 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-3696C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762630 | |||||||
| chr5:112762943 | T | TA | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0283 |
3 | HG00673.hp1 NA19011.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.136-3381dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112762943 | ||||||
| chr5:112763162 | A | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.136-3164A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763162 | |||||||
| chr5:112763214 | G | A | 286 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(283): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.136-3112G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763214 | |||||||
| chr5:112763221 | CA | C | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3097delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112763221 | ||||||
| chr5:112763241 | T | A | 102 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(99): Show |
102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.136-3085T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763241 | |||||||
| chr5:112763252 | A | T | 2 | a0001c0003t0002g0033 a0001c0005t0005g0011 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-3074A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763252 | |||||||
| chr5:112763331 | A | G | 101 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(98): Show |
101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.136-2995A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763331 | |||||||
| chr5:112763362 | GT | G | 203 | a0001c0001t0001g0122 a0001c0001t0001g0194 a0001c0001t0001g0195 others(200): Show |
205 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(202): Show |
intron_variant | MODIFIER | c.136-2954delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112763362 | ||||||
| chr5:112763363 | T | G | 2 | a0002c0004t0002g0013 a0002c0004t0002g0014 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.136-2963T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763363 | |||||||
| chr5:112763396 | C | T | 1 | a0001c0002t0004g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-2930C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763396 | |||||||
| chr5:112763457 | A | C | 1 | a0001c0003t0002g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136-2869A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763457 | |||||||
| chr5:112763765 | T | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-2561T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763765 | |||||||
| chr5:112763766 | A | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-2560A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763766 | |||||||
| chr5:112763799 | G | A | 49 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(46): Show |
51 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.136-2527G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763799 | |||||||
| chr5:112763839 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.136-2487C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763839 | |||||||
| chr5:112763849 | C | T | 1 | a0002c0004t0002g0091 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.136-2477C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763849 | |||||||
| chr5:112763964 | G | A | 1 | a0003c0006t0001g0277 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-2362G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763964 | |||||||
| chr5:112763993 | T | C | 14 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(11): Show |
14 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-2333T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763993 | |||||||
| chr5:112764013 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136-2313G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764013 | |||||||
| chr5:112764033 | C | G | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-2293C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764033 | |||||||
| chr5:112764078 | TA | T | 251 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(248): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.136-2230delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112764078 | ||||||
| chr5:112764245 | C | CA | 7 | a0001c0002t0005g0115 a0001c0002t0009g0125 a0001c0002t0009g0131 others(4): Show |
7 | HG01243.hp2 HG03139.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2063dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112764245 | ||||||
| chr5:112764245 | CA | C | 168 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(165): Show |
170 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(167): Show |
intron_variant | MODIFIER | c.136-2063delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112764245 | ||||||
| chr5:112764311 | G | A | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-2015G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764311 | |||||||
| chr5:112764330 | G | A | 173 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(170): Show |
175 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(172): Show |
intron_variant | MODIFIER | c.136-1996G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764330 | |||||||
| chr5:112764392 | A | G | 2 | a0001c0003t0002g0032 a0001c0003t0002g0033 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.136-1934A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764392 | |||||||
| chr5:112764423 | G | C | 1 | a0001c0001t0001g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.136-1903G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764423 | |||||||
| chr5:112764598 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0247 |
2 | NA18981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.136-1728A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764598 | |||||||
| chr5:112764719 | C | T | 14 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(11): Show |
14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-1607C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764719 | |||||||
| chr5:112764774 | A | T | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.136-1552A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764774 | |||||||
| chr5:112764830 | A | G | 1 | a0002c0004t0002g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.136-1496A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764830 | |||||||
| chr5:112764858 | G | T | 28 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(25): Show |
28 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-1468G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764858 | |||||||
| chr5:112764898 | A | C | 288 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(285): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.136-1428A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764898 | |||||||
| chr5:112765016 | A | C | 2 | a0001c0008t0002g0130 a0001c0030t0002g0129 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136-1310A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765016 | |||||||
| chr5:112765197 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.136-1129T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765197 | |||||||
| chr5:112765285 | T | G | 5 | a0001c0002t0003g0001 a0001c0002t0003g0153 a0001c0002t0003g0154 others(2): Show |
6 | HG00408.hp1 HG02155.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-1041T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765285 | |||||||
| chr5:112765322 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01109.hp2 HG01433.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.136-1004C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765322 | |||||||
| chr5:112765431 | A | G | 3 | a0002c0004t0002g0062 a0002c0004t0002g0089 a0002c0004t0002g0090 |
3 | HG03491.hp1 NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.136-895A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765431 | |||||||
| chr5:112765677 | CAAAGTTC others(3): Show |
C | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-646_136-637del others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112765677 | ||||||
| chr5:112765760 | G | T | 143 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(140): Show |
145 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.136-566G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765760 | |||||||
| chr5:112765799 | G | A | 286 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(283): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.136-527G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765799 | |||||||
| chr5:112765808 | A | T | 1 | a0003c0006t0001g0263 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.136-518A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765808 | |||||||
| chr5:112765815 | C | G | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136-511C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765815 | |||||||
| chr5:112765937 | C | CA | 4 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-388dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112765937 | ||||||
| chr5:112765954 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.136-372A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765954 | |||||||
| chr5:112765976 | A | G | 30 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(27): Show |
32 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.136-350A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765976 | |||||||
| chr5:112766096 | C | A | 216 | a0001c0001t0001g0122 a0001c0001t0001g0194 a0001c0001t0001g0195 others(213): Show |
218 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.136-230C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766096 | |||||||
| chr5:112766143 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0274 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-183A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766143 | |||||||
| chr5:112766162 | C | T | 1 | a0002c0004t0002g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.136-164C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766162 | |||||||
| chr5:112766273 | T | C | 50 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(47): Show |
52 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.136-53T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766273 | |||||||
| chr5:112766534 | C | G | 3 | a0003c0006t0001g0263 a0003c0006t0001g0277 a0003c0006t0001g0278 |
3 | HG01070.hp1 HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.220+124C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112766534 | |||||||
| chr5:112766659 | C | T | 1 | a0002c0004t0002g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.220+249C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112766659 | |||||||
| chr5:112766689 | C | T | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.220+279C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112766689 | |||||||
| chr5:112767038 | G | C | 13 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(10): Show |
13 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-151G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112767038 | |||||||
| chr5:112767465 | T | C | 2 | a0001c0008t0002g0130 a0001c0030t0002g0129 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.422+75T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767465 | |||||||
| chr5:112767526 | A | G | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+136A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767526 | |||||||
| chr5:112767619 | T | C | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422+229T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767619 | |||||||
| chr5:112767632 | T | C | 1 | a0002c0004t0002g0041 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.422+242T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767632 | |||||||
| chr5:112767949 | C | A | 1 | a0002c0004t0002g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.422+559C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767949 | |||||||
| chr5:112767950 | A | T | 1 | a0002c0004t0002g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.422+560A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767950 | |||||||
| chr5:112767983 | G | A | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.422+593G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767983 | |||||||
| chr5:112768043 | CT | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0269 others(6): Show |
9 | HG00639.hp1 HG01070.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+670delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112768043 | ||||||
| chr5:112768230 | A | G | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422+840A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768230 | |||||||
| chr5:112768266 | C | G | 99 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(96): Show |
99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.422+876C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768266 | |||||||
| chr5:112768430 | TATTCAGT others(20): Show |
T | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.422+1041_422+1067d others(29): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768430 | |||||||
| chr5:112768434 | C | G | 1 | a0002c0004t0002g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422+1044C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768434 | |||||||
| chr5:112768537 | T | A | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+1147T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768537 | |||||||
| chr5:112768585 | A | G | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+1195A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768585 | |||||||
| chr5:112768600 | A | G | 98 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.422+1210A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768600 | |||||||
| chr5:112768715 | A | G | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+1325A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768715 | |||||||
| chr5:112768734 | CCCTGTAC others(18): Show |
C | 51 | a0001c0001t0001g0230 a0001c0001t0001g0259 a0001c0002t0001g0286 others(48): Show |
53 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.422+1446_422+1470d others(27): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112768734 | ||||||
| chr5:112768848 | G | A | 1 | a0001c0002t0003g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422+1458G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768848 | |||||||
| chr5:112768863 | A | G | 2 | a0001c0010t0007g0132 a0001c0014t0007g0133 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.422+1473A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768863 | |||||||
| chr5:112768900 | A | G | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.422+1510A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768900 | |||||||
| chr5:112768987 | C | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.422+1597C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768987 | |||||||
| chr5:112769050 | C | CT | 99 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0198 others(96): Show |
99 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.422+1680dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769050 | ||||||
| chr5:112769050 | C | CTT | 35 | a0001c0001t0001g0239 a0001c0001t0001g0242 a0001c0001t0001g0248 others(32): Show |
35 | HG00323.hp1 HG00673.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.422+1679_422+1680d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769050 | ||||||
| chr5:112769050 | C | CTTT | 45 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0002t0001g0286 others(42): Show |
47 | HG00408.hp1 HG00609.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.422+1678_422+1680d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769050 | ||||||
| chr5:112769071 | G | T | 43 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(40): Show |
43 | HG00741.hp2 HG01496.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.422+1681G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769071 | |||||||
| chr5:112769097 | G | GC | 15 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.422+1708dupC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769097 | ||||||
| chr5:112769099 | T | A | 15 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.422+1709T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769099 | |||||||
| chr5:112769113 | G | A | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.422+1723G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769113 | |||||||
| chr5:112769128 | G | A | 3 | a0001c0002t0003g0169 a0001c0002t0003g0170 a0001c0002t0003g0171 |
3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422+1738G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769128 | |||||||
| chr5:112769176 | G | A | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.422+1786G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769176 | |||||||
| chr5:112769379 | T | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.422+1989T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769379 | |||||||
| chr5:112769458 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.422+2068A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769458 | |||||||
| chr5:112769511 | T | G | 49 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(46): Show |
51 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.422+2121T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769511 | |||||||
| chr5:112769515 | T | C | 1 | a0001c0003t0002g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.422+2125T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769515 | |||||||
| chr5:112769520 | TG | T | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.422+2131delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769520 | |||||||
| chr5:112769526 | A | T | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.422+2136A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769526 | |||||||
| chr5:112769712 | A | G | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+2322A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769712 | |||||||
| chr5:112769817 | T | G | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+2427T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769817 | |||||||
| chr5:112769837 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | NA18953.hp2 NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.422+2447G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769837 | |||||||
| chr5:112769918 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.422+2528T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769918 | |||||||
| chr5:112769986 | TTTCCCCT others(5): Show |
T | 7 | a0002c0004t0002g0055 a0002c0004t0002g0082 a0002c0004t0002g0083 others(4): Show |
7 | HG00639.hp2 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.422+2597_422+2608d others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769986 | |||||||
| chr5:112770024 | A | C | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+2634A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770024 | |||||||
| chr5:112770137 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.422+2747A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770137 | |||||||
| chr5:112770229 | C | G | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.422+2839C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770229 | |||||||
| chr5:112770524 | C | T | 1 | a0001c0008t0002g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.422+3134C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770524 | |||||||
| chr5:112770527 | T | C | 4 | a0001c0001t0001g0122 a0001c0001t0004g0121 a0001c0001t0004g0123 others(1): Show |
4 | HG01358.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+3137T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770527 | |||||||
| chr5:112770551 | A | G | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422+3161A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770551 | |||||||
| chr5:112770567 | A | G | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+3177A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770567 | |||||||
| chr5:112770568 | T | A | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.422+3178T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770568 | |||||||
| chr5:112770573 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.422+3183T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770573 | |||||||
| chr5:112770891 | C | A | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.422+3501C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770891 | |||||||
| chr5:112771090 | G | A | 1 | a0001c0002t0003g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.422+3700G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771090 | |||||||
| chr5:112771351 | G | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+3961G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771351 | |||||||
| chr5:112771361 | G | A | 96 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(93): Show |
96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.422+3971G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771361 | |||||||
| chr5:112771432 | T | A | 3 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0078 |
3 | HG00408.hp2 NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.422+4042T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771432 | |||||||
| chr5:112771439 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.422+4049T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771439 | |||||||
| chr5:112771533 | T | C | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.423-4096T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771533 | |||||||
| chr5:112771819 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423-3810A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771819 | |||||||
| chr5:112771907 | T | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-3722T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771907 | |||||||
| chr5:112771999 | T | C | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.423-3630T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771999 | |||||||
| chr5:112772021 | G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.423-3608G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772021 | |||||||
| chr5:112772029 | C | T | 95 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.423-3600C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772029 | |||||||
| chr5:112772384 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0260 |
2 | NA18612.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.423-3245C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772384 | |||||||
| chr5:112772455 | C | G | 3 | a0001c0007t0004g0118 a0001c0007t0004g0119 a0001c0007t0004g0120 |
3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.423-3174C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772455 | |||||||
| chr5:112772472 | C | T | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.423-3157C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772472 | |||||||
| chr5:112772516 | C | CT | 12 | a0001c0001t0001g0240 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.423-3095dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112772516 | ||||||
| chr5:112772516 | CT | C | 28 | a0001c0001t0001g0122 a0001c0001t0001g0194 a0001c0001t0001g0205 others(25): Show |
28 | HG00639.hp2 HG00733.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.423-3095delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112772516 | ||||||
| chr5:112772539 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.423-3090C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772539 | |||||||
| chr5:112772564 | T | C | 2 | a0001c0010t0007g0132 a0001c0014t0007g0133 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.423-3065T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772564 | |||||||
| chr5:112772672 | G | A | 15 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(12): Show |
15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.423-2957G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772672 | |||||||
| chr5:112772737 | G | A | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-2892G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772737 | |||||||
| chr5:112772761 | C | T | 1 | a0001c0010t0007g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.423-2868C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772761 | |||||||
| chr5:112772806 | C | A | 1 | a0001c0003t0002g0080 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.423-2823C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772806 | |||||||
| chr5:112772860 | GAA | G | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-2767_423-2766d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112772860 | ||||||
| chr5:112772863 | A | T | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-2766A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772863 | |||||||
| chr5:112772889 | C | G | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.423-2740C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772889 | |||||||
| chr5:112772984 | C | G | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.423-2645C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772984 | |||||||
| chr5:112773156 | A | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.423-2473A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773156 | |||||||
| chr5:112773168 | T | C | 110 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(107): Show |
110 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.423-2461T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773168 | |||||||
| chr5:112773308 | A | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.423-2321A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773308 | |||||||
| chr5:112773375 | C | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.423-2254C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773375 | |||||||
| chr5:112773497 | G | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.423-2132G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773497 | |||||||
| chr5:112773504 | A | G | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423-2125A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773504 | |||||||
| chr5:112773619 | T | C | 2 | a0001c0002t0004g0092 a0007c0023t0004g0093 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.423-2010T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773619 | |||||||
| chr5:112774082 | G | C | 181 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(178): Show |
183 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(180): Show |
intron_variant | MODIFIER | c.423-1547G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774082 | |||||||
| chr5:112774306 | A | G | 16 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(13): Show |
16 | HG00673.hp2 HG01981.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.423-1323A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774306 | |||||||
| chr5:112774371 | A | G | 2 | a0001c0008t0002g0130 a0001c0030t0002g0129 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.423-1258A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774371 | |||||||
| chr5:112774375 | A | G | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.423-1254A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774375 | |||||||
| chr5:112774464 | A | AT | 17 | a0001c0001t0001g0210 a0001c0001t0001g0252 a0001c0001t0004g0116 others(14): Show |
17 | HG00609.hp1 HG00733.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.423-1145dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112774464 | ||||||
| chr5:112774464 | A | ATT | 89 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(86): Show |
89 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.423-1146_423-1145d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112774464 | ||||||
| chr5:112774464 | A | ATTT | 9 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0243 others(6): Show |
9 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-1147_423-1145d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112774464 | ||||||
| chr5:112774637 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.423-992T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774637 | |||||||
| chr5:112774677 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.423-952A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774677 | |||||||
| chr5:112774736 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423-893C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774736 | |||||||
| chr5:112774963 | G | A | 31 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(28): Show |
33 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.423-666G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774963 | |||||||
| chr5:112774965 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.423-664G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774965 | |||||||
| chr5:112775125 | G | A | 1 | a0001c0002t0003g0156 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.423-504G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775125 | |||||||
| chr5:112775373 | G | A | 285 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.423-256G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775373 | |||||||
| chr5:112775459 | A | G | 2 | a0001c0008t0002g0104 a0013c0028t0002g0105 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.423-170A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775459 | |||||||
| chr5:112775494 | T | A | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.423-135T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775494 | |||||||
| chr5:112775605 | C | CT | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-17dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112775605 | ||||||
| chr5:112775612 | TA | T | 11 | a0001c0001t0001g0205 a0001c0003t0002g0053 a0001c0003t0002g0060 others(8): Show |
11 | HG01243.hp1 HG01515.hp1 HG02293.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.423-4delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112775612 | ||||||
| chr5:112775958 | A | G | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+221A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112775958 | |||||||
| chr5:112776169 | G | C | 97 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(94): Show |
97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.531+432G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776169 | |||||||
| chr5:112776178 | C | T | 3 | a0001c0002t0009g0125 a0001c0002t0009g0131 a0001c0003t0002g0111 |
3 | HG01243.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.531+441C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776178 | |||||||
| chr5:112776325 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.531+588C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776325 | |||||||
| chr5:112776414 | C | T | 1 | a0001c0003t0002g0149 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.531+677C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776414 | |||||||
| chr5:112776416 | A | G | 6 | a0001c0003t0002g0043 a0001c0003t0002g0048 a0001c0003t0002g0050 others(3): Show |
6 | HG02132.hp1 NA18747.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+679A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776416 | |||||||
| chr5:112776659 | G | A | 1 | a0001c0003t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.531+922G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776659 | |||||||
| chr5:112776829 | A | C | 1 | a0001c0007t0004g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.531+1092A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776829 | |||||||
| chr5:112776862 | T | TA | 38 | a0001c0001t0001g0075 a0001c0002t0003g0001 a0001c0002t0003g0002 others(35): Show |
40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.531+1136dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112776862 | ||||||
| chr5:112776870 | A | T | 6 | a0002c0004t0002g0068 a0002c0004t0002g0069 a0002c0004t0002g0070 others(3): Show |
6 | HG01433.hp1 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+1133A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776870 | |||||||
| chr5:112776887 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0260 |
2 | NA18612.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.531+1150A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776887 | |||||||
| chr5:112776895 | CT | C | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+1161delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112776895 | ||||||
| chr5:112776903 | G | A | 10 | a0001c0003t0006g0140 a0001c0003t0006g0141 a0001c0003t0006g0142 others(7): Show |
10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.531+1166G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776903 | |||||||
| chr5:112776939 | A | T | 1 | a0001c0003t0002g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.531+1202A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776939 | |||||||
| chr5:112777158 | G | A | 38 | a0001c0001t0001g0075 a0001c0002t0003g0001 a0001c0002t0003g0002 others(35): Show |
40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.531+1421G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777158 | |||||||
| chr5:112777254 | T | C | 31 | a0001c0002t0008g0184 a0001c0002t0008g0185 a0001c0003t0002g0004 others(28): Show |
31 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.531+1517T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777254 | |||||||
| chr5:112777415 | A | G | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.531+1678A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777415 | |||||||
| chr5:112777500 | T | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+1763T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777500 | |||||||
| chr5:112777559 | A | G | 2 | a0001c0002t0004g0092 a0007c0023t0004g0093 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.531+1822A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777559 | |||||||
| chr5:112777730 | T | C | 12 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(9): Show |
12 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.531+1993T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777730 | |||||||
| chr5:112777830 | A | T | 101 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(98): Show |
101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.531+2093A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777830 | |||||||
| chr5:112777981 | G | A | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+2244G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777981 | |||||||
| chr5:112778038 | C | T | 100 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(97): Show |
100 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.531+2301C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778038 | |||||||
| chr5:112778063 | T | C | 217 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(214): Show |
219 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(216): Show |
intron_variant | MODIFIER | c.531+2326T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778063 | |||||||
| chr5:112778075 | G | A | 100 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.531+2338G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778075 | |||||||
| chr5:112778236 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.531+2499C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778236 | |||||||
| chr5:112778262 | T | A | 13 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(10): Show |
13 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.531+2525T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778262 | |||||||
| chr5:112778307 | C | A | 1 | a0012c0022t0003g0173 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.532-2483C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778307 | |||||||
| chr5:112778309 | A | C | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.532-2481A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778309 | |||||||
| chr5:112778467 | TA | T | 10 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0001t0001g0291 others(7): Show |
10 | HG01975.hp1 HG02622.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.532-2308delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778467 | ||||||
| chr5:112778550 | A | AT | 129 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(126): Show |
129 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(126): Show |
intron_variant | MODIFIER | c.532-2226dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778550 | ||||||
| chr5:112778550 | A | ATT | 7 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
7 | HG00642.hp2 HG01074.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-2227_532-2226d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778550 | ||||||
| chr5:112778551 | T | A | 1 | a0001c0003t0002g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.532-2239T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778551 | |||||||
| chr5:112778681 | G | A | 1 | a0001c0002t0004g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.532-2109G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778681 | |||||||
| chr5:112778688 | A | AGGC | 184 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(181): Show |
186 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(183): Show |
intron_variant | MODIFIER | c.532-2101_532-2100i others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778688 | ||||||
| chr5:112779034 | A | T | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.532-1756A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779034 | |||||||
| chr5:112779641 | T | G | 2 | a0001c0002t0003g0159 a0001c0002t0003g0160 |
2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.532-1149T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779641 | |||||||
| chr5:112779652 | A | G | 1 | a0003c0006t0001g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.532-1138A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779652 | |||||||
| chr5:112779660 | A | G | 1 | a0001c0002t0003g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.532-1130A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779660 | |||||||
| chr5:112779667 | A | AT | 44 | a0001c0001t0001g0075 a0001c0001t0001g0259 a0001c0002t0001g0286 others(41): Show |
46 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.532-1111dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112779667 | ||||||
| chr5:112779726 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.532-1064T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779726 | |||||||
| chr5:112779794 | G | T | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.532-996G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779794 | |||||||
| chr5:112779795 | C | T | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.532-995C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779795 | |||||||
| chr5:112779870 | C | T | 1 | a0001c0002t0003g0076 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.532-920C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779870 | |||||||
| chr5:112779945 | A | G | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0274 |
3 | HG00639.hp1 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.532-845A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779945 | |||||||
| chr5:112780046 | G | T | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.532-744G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780046 | |||||||
| chr5:112780327 | C | T | 134 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(131): Show |
134 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.532-463C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780327 | |||||||
| chr5:112780372 | G | A | 187 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(184): Show |
189 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(186): Show |
intron_variant | MODIFIER | c.532-418G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780372 | |||||||
| chr5:112780406 | T | C | 3 | a0001c0007t0004g0118 a0001c0007t0004g0119 a0001c0007t0004g0120 |
3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.532-384T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780406 | |||||||
| chr5:112780758 | T | C | 2 | a0001c0008t0002g0130 a0001c0030t0002g0129 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.532-32T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780758 | |||||||
| chr5:112780935 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+32C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780935 | |||||||
| chr5:112780953 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.645+50A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780953 | |||||||
| chr5:112780964 | C | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+61C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780964 | |||||||
| chr5:112780981 | A | G | 1 | a0002c0004t0002g0090 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.645+78A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780981 | |||||||
| chr5:112781032 | A | C | 29 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(26): Show |
29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.645+129A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781032 | |||||||
| chr5:112781076 | A | G | 103 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(100): Show |
103 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.645+173A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781076 | |||||||
| chr5:112781213 | C | T | 1 | a0003c0006t0001g0263 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.645+310C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781213 | |||||||
| chr5:112781526 | G | T | 2 | a0001c0002t0003g0001 a0011c0021t0003g0164 |
3 | HG00408.hp1 NA18983.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.645+623G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781526 | |||||||
| chr5:112781549 | A | G | 1 | a0001c0003t0002g0015 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.645+646A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781549 | |||||||
| chr5:112781763 | A | AT | 49 | a0001c0001t0001g0075 a0001c0001t0001g0255 a0001c0001t0001g0259 others(46): Show |
51 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.645+875dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112781763 | ||||||
| chr5:112781763 | AT | A | 12 | a0001c0001t0001g0265 a0001c0003t0006g0140 a0001c0003t0006g0141 others(9): Show |
12 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.645+875delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112781763 | ||||||
| chr5:112781831 | G | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0211 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.645+928G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781831 | |||||||
| chr5:112781852 | C | T | 1 | a0001c0002t0003g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.645+949C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781852 | |||||||
| chr5:112781902 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+999C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781902 | |||||||
| chr5:112781934 | A | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0232 a0010c0017t0001g0197 |
3 | NA18948.hp2 NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.645+1031A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781934 | |||||||
| chr5:112781935 | T | C | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+1032T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781935 | |||||||
| chr5:112781981 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+1078G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781981 | |||||||
| chr5:112782074 | G | A | 1 | a0001c0002t0003g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.645+1171G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782074 | |||||||
| chr5:112782077 | G | A | 8 | a0001c0002t0004g0022 a0001c0002t0004g0023 a0001c0002t0004g0024 others(5): Show |
8 | HG02258.hp2 HG02559.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+1174G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782077 | |||||||
| chr5:112782194 | A | G | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+1291A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782194 | |||||||
| chr5:112782244 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+1341C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782244 | |||||||
| chr5:112782276 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+1373C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782276 | |||||||
| chr5:112782482 | A | G | 1 | a0001c0003t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645+1579A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782482 | |||||||
| chr5:112782498 | G | A | 174 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(171): Show |
176 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.645+1595G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782498 | |||||||
| chr5:112782556 | T | G | 1 | a0001c0001t0001g0265 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.645+1653T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782556 | |||||||
| chr5:112782582 | C | T | 1 | a0006c0012t0002g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.645+1679C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782582 | |||||||
| chr5:112782583 | G | A | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.645+1680G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782583 | |||||||
| chr5:112782641 | G | A | 78 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(75): Show |
78 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.645+1738G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782641 | |||||||
| chr5:112782766 | A | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.645+1863A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782766 | |||||||
| chr5:112782852 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645+1949T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782852 | |||||||
| chr5:112782857 | A | T | 1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.645+1954A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782857 | |||||||
| chr5:112783050 | G | T | 1 | a0002c0004t0002g0042 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.645+2147G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783050 | |||||||
| chr5:112783094 | G | A | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+2191G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783094 | |||||||
| chr5:112783225 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.645+2322T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783225 | |||||||
| chr5:112783259 | C | T | 94 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(91): Show |
94 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.645+2356C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783259 | |||||||
| chr5:112783378 | A | G | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.645+2475A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783378 | |||||||
| chr5:112783435 | T | G | 29 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(26): Show |
29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.645+2532T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783435 | |||||||
| chr5:112783510 | A | C | 44 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0001g0259 others(41): Show |
46 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.645+2607A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783510 | |||||||
| chr5:112783630 | C | CA | 20 | a0001c0002t0003g0153 a0001c0002t0003g0154 a0001c0002t0003g0155 others(17): Show |
20 | HG01243.hp1 HG02056.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.645+2745dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783630 | ||||||
| chr5:112783765 | C | CA | 18 | a0001c0001t0004g0116 a0001c0002t0003g0001 a0001c0002t0003g0153 others(15): Show |
19 | HG00408.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.645+2881dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783765 | ||||||
| chr5:112783765 | CA | C | 32 | a0001c0001t0001g0255 a0001c0002t0001g0286 a0001c0002t0003g0174 others(29): Show |
32 | HG00741.hp2 HG01515.hp1 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.645+2881delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783765 | ||||||
| chr5:112783785 | GAGAA | G | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+2889_645+2892d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783785 | ||||||
| chr5:112783826 | C | G | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.645+2923C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783826 | |||||||
| chr5:112783896 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0004g0124 |
2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.645+2993A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783896 | |||||||
| chr5:112784460 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+3557A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784460 | |||||||
| chr5:112784515 | C | T | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.645+3612C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784515 | |||||||
| chr5:112784628 | C | T | 1 | a0001c0002t0008g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645+3725C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784628 | |||||||
| chr5:112784797 | C | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.645+3894C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784797 | |||||||
| chr5:112784892 | C | G | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.645+3989C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784892 | |||||||
| chr5:112784913 | T | C | 1 | a0002c0004t0002g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.645+4010T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784913 | |||||||
| chr5:112784944 | C | A | 1 | a0001c0003t0002g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.645+4041C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784944 | |||||||
| chr5:112785013 | A | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+4110A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112785013 | |||||||
| chr5:112785557 | C | T | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.645+4654C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112785557 | |||||||
| chr5:112786015 | A | T | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.645+5112A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786015 | |||||||
| chr5:112786261 | G | GT | 41 | a0001c0003t0002g0015 a0002c0004t0002g0016 a0002c0004t0002g0034 others(38): Show |
41 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.645+5364dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786261 | ||||||
| chr5:112786390 | G | T | 12 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.645+5487G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786390 | |||||||
| chr5:112786687 | T | G | 1 | a0010c0017t0001g0197 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.646-5759T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786687 | |||||||
| chr5:112786835 | G | C | 102 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(99): Show |
102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.646-5611G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786835 | |||||||
| chr5:112786873 | C | CCTTTTT | 14 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(11): Show |
14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.646-5560_646-5555d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786873 | ||||||
| chr5:112786873 | C | G | 1 | a0001c0003t0006g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.646-5573C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786873 | |||||||
| chr5:112786886 | C | CT | 11 | a0001c0002t0001g0286 a0001c0002t0004g0188 a0001c0002t0004g0189 others(8): Show |
11 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-5541dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786886 | ||||||
| chr5:112786886 | C | CTT | 40 | a0001c0001t0001g0243 a0001c0001t0001g0259 a0001c0002t0001g0287 others(37): Show |
42 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.646-5542_646-5541d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786886 | ||||||
| chr5:112786890 | T | C | 1 | a0001c0002t0008g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646-5556T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786890 | |||||||
| chr5:112786906 | GAGTC | G | 95 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.646-5537_646-5534d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786906 | ||||||
| chr5:112786910 | C | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0271 |
2 | HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.646-5536C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786910 | |||||||
| chr5:112787168 | G | A | 17 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(14): Show |
17 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.646-5278G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787168 | |||||||
| chr5:112787169 | T | C | 1 | a0001c0003t0002g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.646-5277T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787169 | |||||||
| chr5:112787184 | G | A | 1 | a0014c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-5262G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787184 | |||||||
| chr5:112787312 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.646-5134G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787312 | |||||||
| chr5:112787329 | A | G | 1 | a0001c0027t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.646-5117A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787329 | |||||||
| chr5:112787339 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.646-5107A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787339 | |||||||
| chr5:112787448 | TTCTG | T | 39 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(36): Show |
39 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.646-4996_646-4993d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112787448 | ||||||
| chr5:112787472 | G | C | 1 | a0001c0002t0003g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.646-4974G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787472 | |||||||
| chr5:112787542 | C | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646-4904C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787542 | |||||||
| chr5:112787967 | CAT | C | 13 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(10): Show |
13 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.646-4478_646-4477d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787967 | |||||||
| chr5:112787993 | G | A | 1 | a0004c0009t0002g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.646-4453G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787993 | |||||||
| chr5:112788309 | A | T | 2 | a0001c0001t0001g0227 a0001c0001t0004g0124 |
2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.646-4137A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788309 | |||||||
| chr5:112788415 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.646-4031A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788415 | |||||||
| chr5:112788509 | A | C | 1 | a0001c0002t0003g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.646-3937A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788509 | |||||||
| chr5:112788522 | A | G | 33 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(30): Show |
33 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.646-3924A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788522 | |||||||
| chr5:112788590 | A | G | 1 | a0002c0004t0002g0083 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-3856A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788590 | |||||||
| chr5:112788672 | T | C | 217 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(214): Show |
219 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(216): Show |
intron_variant | MODIFIER | c.646-3774T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788672 | |||||||
| chr5:112788708 | C | T | 2 | a0002c0004t0002g0016 a0008c0032t0002g0017 |
2 | HG00323.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.646-3738C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788708 | |||||||
| chr5:112788783 | G | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-3663G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788783 | |||||||
| chr5:112788847 | A | G | 2 | a0001c0002t0003g0186 a0001c0002t0003g0187 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.646-3599A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788847 | |||||||
| chr5:112788883 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.646-3563A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788883 | |||||||
| chr5:112789031 | G | A | 1 | a0001c0003t0002g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.646-3415G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789031 | |||||||
| chr5:112789080 | A | G | 1 | a0001c0031t0002g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.646-3366A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789080 | |||||||
| chr5:112789100 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.646-3346A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789100 | |||||||
| chr5:112789217 | A | G | 1 | a0001c0003t0002g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.646-3229A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789217 | |||||||
| chr5:112789365 | A | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG00642.hp2 HG01074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.646-3081A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789365 | |||||||
| chr5:112789600 | T | A | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646-2846T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789600 | |||||||
| chr5:112789615 | G | A | 1 | a0001c0002t0015g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.646-2831G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789615 | |||||||
| chr5:112789722 | A | G | 90 | a0001c0001t0001g0122 a0001c0001t0001g0259 a0001c0001t0004g0116 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.646-2724A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789722 | |||||||
| chr5:112789857 | A | AT | 28 | a0001c0001t0001g0075 a0001c0001t0001g0248 a0001c0001t0001g0264 others(25): Show |
28 | HG00323.hp1 HG00673.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.646-2576dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112789857 | ||||||
| chr5:112789857 | AT | A | 38 | a0001c0001t0001g0217 a0001c0001t0004g0124 a0001c0002t0003g0001 others(35): Show |
40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.646-2576delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112789857 | ||||||
| chr5:112789946 | G | A | 16 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(13): Show |
16 | HG02132.hp1 HG02155.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-2500G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789946 | |||||||
| chr5:112789996 | A | G | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.646-2450A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789996 | |||||||
| chr5:112790000 | C | T | 7 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-2446C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790000 | |||||||
| chr5:112790314 | T | G | 2 | a0001c0001t0001g0285 a0001c0002t0013g0003 |
2 | HG02056.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.646-2132T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790314 | |||||||
| chr5:112790586 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.646-1860C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790586 | |||||||
| chr5:112790631 | G | A | 21 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(18): Show |
21 | HG00741.hp2 HG02132.hp1 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.646-1815G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790631 | |||||||
| chr5:112790648 | T | C | 40 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(37): Show |
42 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.646-1798T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790648 | |||||||
| chr5:112791032 | CAT | C | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1411_646-1410d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112791032 | ||||||
| chr5:112791118 | T | G | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.646-1328T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791118 | |||||||
| chr5:112791156 | A | AAC | 4 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1272_646-1271d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112791156 | ||||||
| chr5:112791156 | A | C | 1 | a0001c0003t0002g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.646-1290A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791156 | |||||||
| chr5:112791278 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0004g0121 a0001c0001t0004g0123 |
3 | HG01361.hp1 HG02257.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.646-1168C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791278 | |||||||
| chr5:112791331 | C | T | 1 | a0002c0004t0002g0041 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.646-1115C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791331 | |||||||
| chr5:112791482 | T | C | 16 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(13): Show |
16 | HG02132.hp1 HG02155.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-964T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791482 | |||||||
| chr5:112791566 | G | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-880G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791566 | |||||||
| chr5:112791633 | C | T | 2 | a0002c0004t0002g0013 a0002c0004t0002g0014 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.646-813C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791633 | |||||||
| chr5:112791756 | G | A | 9 | a0001c0003t0006g0140 a0001c0003t0006g0141 a0001c0003t0006g0142 others(6): Show |
9 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-690G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791756 | |||||||
| chr5:112792139 | G | A | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.646-307G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112792139 | |||||||
| chr5:112792245 | C | T | 5 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0163 others(2): Show |
5 | HG02071.hp1 NA18612.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-201C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112792245 | |||||||
| chr5:112792552 | T | C | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+23T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792552 | |||||||
| chr5:112792617 | T | C | 12 | a0001c0002t0003g0001 a0001c0002t0003g0153 a0001c0002t0003g0154 others(9): Show |
13 | HG00408.hp1 HG02071.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.729+88T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792617 | |||||||
| chr5:112792712 | C | T | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+183C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792712 | |||||||
| chr5:112792827 | T | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+298T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792827 | |||||||
| chr5:112792867 | A | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.729+338A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792867 | |||||||
| chr5:112792960 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.729+431C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792960 | |||||||
| chr5:112792976 | A | G | 39 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(36): Show |
41 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.729+447A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792976 | |||||||
| chr5:112793048 | C | T | 1 | a0001c0002t0003g0159 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.729+519C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793048 | |||||||
| chr5:112793057 | A | T | 1 | a0001c0003t0002g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.729+528A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793057 | |||||||
| chr5:112793146 | C | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+617C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793146 | |||||||
| chr5:112793373 | A | G | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.729+844A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793373 | |||||||
| chr5:112793406 | C | G | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.729+877C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793406 | |||||||
| chr5:112793497 | AC | A | 193 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(190): Show |
195 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(192): Show |
intron_variant | MODIFIER | c.729+969delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793497 | |||||||
| chr5:112793532 | A | C | 1 | a0001c0001t0001g0268 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.729+1003A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793532 | |||||||
| chr5:112793968 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+1439C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793968 | |||||||
| chr5:112793988 | G | C | 2 | a0001c0001t0004g0261 a0001c0001t0004g0262 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.729+1459G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793988 | |||||||
| chr5:112794042 | TA | T | 29 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(26): Show |
29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.729+1527delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112794042 | ||||||
| chr5:112794056 | AG | A | 176 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(173): Show |
178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.729+1529delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112794056 | ||||||
| chr5:112794057 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0255 a0001c0002t0003g0161 |
3 | HG01257.hp2 HG01993.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.729+1528G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794057 | |||||||
| chr5:112794183 | C | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG02071.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.729+1654C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794183 | |||||||
| chr5:112794265 | G | A | 1 | a0002c0004t0002g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.729+1736G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794265 | |||||||
| chr5:112794271 | A | G | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.729+1742A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794271 | |||||||
| chr5:112794362 | G | A | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.729+1833G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794362 | |||||||
| chr5:112794378 | C | A | 1 | a0001c0016t0001g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.729+1849C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794378 | |||||||
| chr5:112794389 | C | A | 198 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(195): Show |
200 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(197): Show |
intron_variant | MODIFIER | c.729+1860C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794389 | |||||||
| chr5:112794415 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+1886A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794415 | |||||||
| chr5:112794449 | A | G | 10 | a0001c0008t0002g0100 a0001c0008t0002g0104 a0001c0008t0002g0130 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.729+1920A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794449 | |||||||
| chr5:112794580 | C | T | 5 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(2): Show |
5 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+2051C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794580 | |||||||
| chr5:112794749 | T | C | 3 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0012 |
3 | HG02486.hp1 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.729+2220T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794749 | |||||||
| chr5:112794755 | C | G | 1 | a0008c0032t0002g0017 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.729+2226C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794755 | |||||||
| chr5:112795058 | G | T | 12 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.729+2529G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795058 | |||||||
| chr5:112795278 | G | A | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.729+2749G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795278 | |||||||
| chr5:112795323 | G | A | 2 | a0002c0004t0002g0089 a0002c0004t0002g0090 |
2 | NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.729+2794G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795323 | |||||||
| chr5:112795522 | A | G | 23 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(20): Show |
23 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.729+2993A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795522 | |||||||
| chr5:112795591 | A | G | 112 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(109): Show |
112 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.729+3062A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795591 | |||||||
| chr5:112795812 | G | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+3283G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795812 | |||||||
| chr5:112796006 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+3477C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796006 | |||||||
| chr5:112796090 | A | G | 104 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(101): Show |
104 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.729+3561A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796090 | |||||||
| chr5:112796262 | A | G | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.729+3733A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796262 | |||||||
| chr5:112796367 | C | A | 1 | a0001c0002t0003g0167 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.729+3838C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796367 | |||||||
| chr5:112797010 | T | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | NA18953.hp2 NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.730-4269T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797010 | |||||||
| chr5:112797139 | C | T | 1 | a0007c0023t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.730-4140C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797139 | |||||||
| chr5:112797202 | T | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.730-4077T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797202 | |||||||
| chr5:112797251 | A | G | 17 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(14): Show |
17 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.730-4028A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797251 | |||||||
| chr5:112797267 | AT | A | 4 | a0001c0003t0002g0053 a0001c0003t0002g0056 a0001c0003t0002g0057 others(1): Show |
4 | HG01106.hp1 HG01169.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-4008delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112797267 | ||||||
| chr5:112797311 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.730-3968A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797311 | |||||||
| chr5:112797393 | T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-3886T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797393 | |||||||
| chr5:112797441 | A | G | 28 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(25): Show |
28 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.730-3838A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797441 | |||||||
| chr5:112797487 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.730-3792T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797487 | |||||||
| chr5:112797494 | T | C | 1 | a0001c0002t0009g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.730-3785T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797494 | |||||||
| chr5:112797499 | G | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-3780G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797499 | |||||||
| chr5:112797787 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.730-3492G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797787 | |||||||
| chr5:112798150 | A | G | 2 | a0006c0012t0002g0101 a0006c0012t0002g0102 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.730-3129A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798150 | |||||||
| chr5:112798345 | G | A | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.730-2934G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798345 | |||||||
| chr5:112798480 | A | G | 1 | a0001c0003t0002g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730-2799A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798480 | |||||||
| chr5:112798660 | T | C | 1 | a0001c0003t0002g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730-2619T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798660 | |||||||
| chr5:112798931 | C | T | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.730-2348C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798931 | |||||||
| chr5:112798946 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.730-2333A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798946 | |||||||
| chr5:112798983 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-2296G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798983 | |||||||
| chr5:112799133 | G | A | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-2146G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799133 | |||||||
| chr5:112799140 | C | T | 86 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(83): Show |
88 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.730-2139C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799140 | |||||||
| chr5:112799183 | C | CA | 153 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0195 others(150): Show |
154 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.730-2075dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112799183 | ||||||
| chr5:112799183 | C | CAA | 32 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0243 others(29): Show |
33 | HG00408.hp1 HG00741.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.730-2076_730-2075d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112799183 | ||||||
| chr5:112799206 | G | A | 36 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(33): Show |
36 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.730-2073G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799206 | |||||||
| chr5:112799255 | C | G | 1 | a0001c0003t0002g0047 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.730-2024C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799255 | |||||||
| chr5:112799370 | T | C | 288 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(285): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.730-1909T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799370 | |||||||
| chr5:112799393 | G | A | 103 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(100): Show |
103 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.730-1886G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799393 | |||||||
| chr5:112799425 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-1854C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799425 | |||||||
| chr5:112799429 | C | T | 7 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.730-1850C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799429 | |||||||
| chr5:112799484 | T | C | 24 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(21): Show |
24 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.730-1795T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799484 | |||||||
| chr5:112799498 | A | G | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730-1781A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799498 | |||||||
| chr5:112799529 | T | C | 15 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.730-1750T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799529 | |||||||
| chr5:112799647 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.730-1632A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799647 | |||||||
| chr5:112799800 | C | T | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.730-1479C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799800 | |||||||
| chr5:112799802 | T | A | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.730-1477T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799802 | |||||||
| chr5:112799829 | C | G | 2 | a0003c0006t0001g0277 a0003c0006t0001g0278 |
2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.730-1450C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799829 | |||||||
| chr5:112799866 | C | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-1413C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799866 | |||||||
| chr5:112800040 | A | G | 101 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(98): Show |
101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.730-1239A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800040 | |||||||
| chr5:112800194 | T | TA | 7 | a0001c0008t0002g0104 a0004c0009t0002g0103 a0004c0009t0002g0106 others(4): Show |
7 | HG01243.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.730-1082dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112800194 | ||||||
| chr5:112800235 | T | C | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.730-1044T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800235 | |||||||
| chr5:112800278 | G | A | 50 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(47): Show |
50 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.730-1001G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800278 | |||||||
| chr5:112800507 | A | G | 101 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(98): Show |
101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.730-772A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800507 | |||||||
| chr5:112800542 | T | C | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.730-737T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800542 | |||||||
| chr5:112800618 | T | C | 9 | a0001c0003t0006g0140 a0001c0003t0006g0141 a0001c0003t0006g0142 others(6): Show |
9 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.730-661T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800618 | |||||||
| chr5:112800809 | C | T | 1 | a0001c0002t0003g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.730-470C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800809 | |||||||
| chr5:112800865 | C | A | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730-414C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800865 | |||||||
| chr5:112801040 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.730-239A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112801040 | |||||||
| chr5:112801250 | A | T | 7 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.730-29A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112801250 | |||||||
| chr5:112801638 | G | GT | 13 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(10): Show |
13 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+263dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112801638 | ||||||
| chr5:112801652 | C | A | 7 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(4): Show |
7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+269C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112801652 | |||||||
| chr5:112801663 | A | G | 1 | a0001c0031t0002g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.834+280A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112801663 | |||||||
| chr5:112802008 | A | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.834+625A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802008 | |||||||
| chr5:112802492 | G | A | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+1109G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802492 | |||||||
| chr5:112802530 | A | G | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.834+1147A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802530 | |||||||
| chr5:112802667 | A | G | 1 | a0001c0008t0002g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.834+1284A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802667 | |||||||
| chr5:112802676 | A | G | 2 | a0001c0002t0009g0125 a0001c0002t0009g0131 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.834+1293A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802676 | |||||||
| chr5:112802736 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.834+1353A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802736 | |||||||
| chr5:112802845 | A | G | 17 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(14): Show |
17 | HG01081.hp1 HG01106.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.834+1462A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802845 | |||||||
| chr5:112802870 | A | T | 5 | a0001c0003t0002g0108 a0001c0003t0002g0110 a0001c0003t0002g0111 others(2): Show |
5 | HG02818.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+1487A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802870 | |||||||
| chr5:112803037 | G | A | 216 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(213): Show |
218 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.834+1654G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803037 | |||||||
| chr5:112803046 | A | T | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+1663A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803046 | |||||||
| chr5:112803094 | G | T | 1 | a0001c0003t0002g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.834+1711G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803094 | |||||||
| chr5:112803161 | T | G | 1 | a0001c0003t0002g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.834+1778T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803161 | |||||||
| chr5:112803191 | G | C | 180 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(177): Show |
182 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(179): Show |
intron_variant | MODIFIER | c.834+1808G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803191 | |||||||
| chr5:112803308 | A | T | 8 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(5): Show |
8 | HG01358.hp1 HG01361.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+1925A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803308 | |||||||
| chr5:112803365 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+1982A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803365 | |||||||
| chr5:112803401 | A | G | 1 | a0002c0004t0002g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.834+2018A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803401 | |||||||
| chr5:112803694 | G | A | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+2311G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803694 | |||||||
| chr5:112803727 | A | G | 104 | a0001c0001t0001g0122 a0001c0001t0001g0259 a0001c0001t0001g0269 others(101): Show |
106 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.834+2344A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803727 | |||||||
| chr5:112803797 | T | G | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+2414T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803797 | |||||||
| chr5:112803846 | A | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+2463A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803846 | |||||||
| chr5:112803953 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.834+2570A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803953 | |||||||
| chr5:112803990 | A | G | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+2607A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803990 | |||||||
| chr5:112804048 | A | G | 100 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.834+2665A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804048 | |||||||
| chr5:112804068 | A | G | 1 | a0002c0025t0002g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.834+2685A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804068 | |||||||
| chr5:112804211 | G | A | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+2828G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804211 | |||||||
| chr5:112804325 | A | G | 32 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(29): Show |
32 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.834+2942A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804325 | |||||||
| chr5:112804335 | G | C | 2 | a0001c0003t0002g0045 a0001c0019t0002g0079 |
2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.834+2952G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804335 | |||||||
| chr5:112804390 | A | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.834+3007A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804390 | |||||||
| chr5:112804415 | G | A | 1 | a0001c0003t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.834+3032G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804415 | |||||||
| chr5:112804538 | C | G | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+3155C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804538 | |||||||
| chr5:112804610 | C | T | 1 | a0001c0002t0003g0181 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.834+3227C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804610 | |||||||
| chr5:112804671 | C | T | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+3288C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804671 | |||||||
| chr5:112804685 | A | C | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+3302A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804685 | |||||||
| chr5:112804772 | T | C | 14 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0209 others(11): Show |
14 | HG01071.hp1 HG01975.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+3389T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804772 | |||||||
| chr5:112804873 | T | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0247 |
2 | NA18981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.834+3490T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804873 | |||||||
| chr5:112804879 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.834+3496G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804879 | |||||||
| chr5:112805052 | A | G | 8 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0212 others(5): Show |
8 | HG01071.hp1 HG01975.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+3669A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805052 | |||||||
| chr5:112805075 | A | G | 11 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(8): Show |
11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+3692A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805075 | |||||||
| chr5:112805244 | T | C | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+3861T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805244 | |||||||
| chr5:112805417 | C | G | 2 | a0002c0004t0002g0016 a0008c0032t0002g0017 |
2 | HG00323.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.834+4034C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805417 | |||||||
| chr5:112805456 | G | A | 14 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(11): Show |
14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+4073G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805456 | |||||||
| chr5:112805602 | T | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.834+4219T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805602 | |||||||
| chr5:112805699 | T | C | 1 | a0001c0002t0003g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.834+4316T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805699 | |||||||
| chr5:112805853 | T | C | 1 | a0001c0002t0003g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.834+4470T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805853 | |||||||
| chr5:112805969 | A | G | 2 | a0001c0003t0002g0045 a0001c0019t0002g0079 |
2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.834+4586A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805969 | |||||||
| chr5:112806012 | C | G | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+4629C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806012 | |||||||
| chr5:112806116 | G | A | 13 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(10): Show |
13 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.834+4733G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806116 | |||||||
| chr5:112806124 | C | T | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+4741C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806124 | |||||||
| chr5:112806206 | G | A | 1 | a0001c0003t0002g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.834+4823G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806206 | |||||||
| chr5:112806339 | T | C | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+4956T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806339 | |||||||
| chr5:112806349 | C | G | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+4966C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806349 | |||||||
| chr5:112806552 | C | CTTTA | 58 | a0001c0001t0001g0122 a0001c0001t0001g0202 a0001c0001t0001g0205 others(55): Show |
58 | HG00609.hp1 HG00642.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.834+5208_834+5211d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | ||||||
| chr5:112806552 | C | CTTTATTT others(1): Show |
16 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(13): Show |
18 | HG00408.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.834+5204_834+5211d others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | ||||||
| chr5:112806552 | C | CTTTATTT others(5): Show |
2 | a0001c0002t0004g0026 a0001c0002t0004g0031 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.834+5200_834+5211d others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | ||||||
| chr5:112806552 | CTTTA | C | 54 | a0001c0001t0001g0249 a0001c0001t0001g0251 a0001c0001t0001g0256 others(51): Show |
54 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.834+5208_834+5211d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | ||||||
| chr5:112806552 | CTTTATTT others(1): Show |
C | 13 | a0001c0001t0001g0211 a0001c0002t0004g0188 a0001c0002t0004g0189 others(10): Show |
13 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+5204_834+5211d others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | ||||||
| chr5:112806552 | CTTTATTT others(9): Show |
C | 2 | a0001c0010t0007g0132 a0001c0014t0007g0133 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.834+5196_834+5211d others(18): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | ||||||
| chr5:112806579 | T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5196T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806579 | |||||||
| chr5:112806583 | T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5200T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806583 | |||||||
| chr5:112806587 | T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5204T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806587 | |||||||
| chr5:112806591 | T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5208T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806591 | |||||||
| chr5:112806722 | G | T | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+5339G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806722 | |||||||
| chr5:112806962 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.834+5579A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806962 | |||||||
| chr5:112807000 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0210 |
2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.834+5617G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807000 | |||||||
| chr5:112807136 | G | GA | 66 | a0001c0001t0001g0220 a0001c0001t0001g0231 a0001c0001t0001g0259 others(63): Show |
68 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.834+5769dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112807136 | ||||||
| chr5:112807136 | G | GAA | 7 | a0001c0002t0003g0170 a0001c0002t0005g0126 a0001c0002t0005g0127 others(4): Show |
7 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+5768_834+5769d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112807136 | ||||||
| chr5:112807188 | C | T | 3 | a0001c0003t0002g0032 a0001c0003t0002g0033 a0001c0029t0002g0018 |
3 | HG02451.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.834+5805C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807188 | |||||||
| chr5:112807217 | C | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+5834C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807217 | |||||||
| chr5:112807312 | A | G | 8 | a0001c0002t0003g0166 a0001c0002t0003g0169 a0001c0002t0003g0170 others(5): Show |
8 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+5929A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807312 | |||||||
| chr5:112807485 | A | G | 1 | a0007c0023t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.834+6102A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807485 | |||||||
| chr5:112807486 | T | G | 3 | a0001c0007t0004g0118 a0001c0007t0004g0119 a0001c0007t0004g0120 |
3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.834+6103T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807486 | |||||||
| chr5:112807503 | T | C | 1 | a0004c0009t0002g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834+6120T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807503 | |||||||
| chr5:112807542 | T | C | 1 | a0001c0002t0003g0159 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.834+6159T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807542 | |||||||
| chr5:112807584 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.834+6201C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807584 | |||||||
| chr5:112807924 | G | A | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+6541G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807924 | |||||||
| chr5:112808008 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.834+6625A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808008 | |||||||
| chr5:112808048 | G | T | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+6665G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808048 | |||||||
| chr5:112808090 | G | A | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+6707G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808090 | |||||||
| chr5:112808124 | C | T | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+6741C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808124 | |||||||
| chr5:112808154 | C | T | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+6771C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808154 | |||||||
| chr5:112808163 | A | T | 35 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0153 others(32): Show |
37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+6780A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808163 | |||||||
| chr5:112808326 | A | G | 104 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(101): Show |
104 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.834+6943A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808326 | |||||||
| chr5:112808487 | A | T | 1 | a0001c0002t0004g0190 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.835-7008A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808487 | |||||||
| chr5:112808542 | G | A | 1 | a0001c0003t0002g0060 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.835-6953G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808542 | |||||||
| chr5:112808607 | C | T | 1 | a0001c0003t0002g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.835-6888C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808607 | |||||||
| chr5:112808627 | G | A | 2 | a0006c0012t0002g0101 a0006c0012t0002g0102 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.835-6868G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808627 | |||||||
| chr5:112808714 | A | C | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.835-6781A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808714 | |||||||
| chr5:112808747 | A | T | 98 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.835-6748A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808747 | |||||||
| chr5:112809197 | C | CA | 25 | a0001c0001t0001g0237 a0001c0002t0003g0166 a0001c0002t0003g0169 others(22): Show |
25 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.835-6283dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112809197 | ||||||
| chr5:112809257 | T | C | 213 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(210): Show |
215 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(212): Show |
intron_variant | MODIFIER | c.835-6238T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809257 | |||||||
| chr5:112809564 | C | A | 95 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.835-5931C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809564 | |||||||
| chr5:112809709 | G | A | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835-5786G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809709 | |||||||
| chr5:112809767 | C | T | 1 | a0002c0004t0002g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.835-5728C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809767 | |||||||
| chr5:112810420 | A | G | 80 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(77): Show |
80 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.835-5075A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810420 | |||||||
| chr5:112810484 | A | G | 19 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(16): Show |
19 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.835-5011A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810484 | |||||||
| chr5:112810500 | T | G | 98 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.835-4995T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810500 | |||||||
| chr5:112810508 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.835-4987C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810508 | |||||||
| chr5:112810540 | G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.835-4955G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810540 | |||||||
| chr5:112810567 | C | T | 7 | a0001c0003t0002g0043 a0001c0003t0002g0045 a0001c0003t0002g0050 others(4): Show |
7 | HG02132.hp1 NA18747.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-4928C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810567 | |||||||
| chr5:112810571 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.835-4924A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810571 | |||||||
| chr5:112810625 | G | A | 3 | a0001c0003t0002g0032 a0001c0003t0002g0033 a0001c0029t0002g0018 |
3 | HG02451.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.835-4870G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810625 | |||||||
| chr5:112810647 | T | TA | 12 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0212 others(9): Show |
12 | HG01071.hp1 HG01975.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-4848_835-4847i others(3): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810647 | |||||||
| chr5:112810686 | A | C | 1 | a0002c0004t0002g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.835-4809A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810686 | |||||||
| chr5:112810879 | G | A | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-4616G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810879 | |||||||
| chr5:112811023 | TCA | T | 163 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(160): Show |
165 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(162): Show |
intron_variant | MODIFIER | c.835-4457_835-4456d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112811023 | ||||||
| chr5:112811040 | A | C | 7 | a0001c0003t0002g0151 a0001c0003t0006g0142 a0001c0003t0006g0144 others(4): Show |
7 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-4455A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811040 | |||||||
| chr5:112811074 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.835-4421C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811074 | |||||||
| chr5:112811402 | A | G | 11 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(8): Show |
11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.835-4093A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811402 | |||||||
| chr5:112811509 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.835-3986G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811509 | |||||||
| chr5:112811684 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.835-3811G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811684 | |||||||
| chr5:112811944 | T | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.835-3551T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811944 | |||||||
| chr5:112812055 | G | A | 1 | a0001c0002t0003g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.835-3440G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812055 | |||||||
| chr5:112812075 | G | C | 3 | a0001c0002t0003g0169 a0001c0002t0003g0170 a0001c0002t0003g0171 |
3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.835-3420G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812075 | |||||||
| chr5:112812106 | G | C | 3 | a0001c0002t0003g0169 a0001c0002t0003g0170 a0001c0002t0003g0171 |
3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.835-3389G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812106 | |||||||
| chr5:112812209 | A | G | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-3286A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812209 | |||||||
| chr5:112812252 | T | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.835-3243T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812252 | |||||||
| chr5:112812454 | AT | A | 3 | a0001c0002t0004g0022 a0001c0002t0004g0023 a0001c0002t0004g0024 |
3 | HG02559.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.835-3038delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112812454 | ||||||
| chr5:112812535 | G | A | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.835-2960G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812535 | |||||||
| chr5:112812626 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.835-2869A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812626 | |||||||
| chr5:112812934 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.835-2561C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812934 | |||||||
| chr5:112812976 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.835-2519G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812976 | |||||||
| chr5:112813049 | G | C | 1 | a0001c0005t0005g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.835-2446G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813049 | |||||||
| chr5:112813192 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.835-2303A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813192 | |||||||
| chr5:112813341 | G | T | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.835-2154G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813341 | |||||||
| chr5:112813342 | C | T | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.835-2153C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813342 | |||||||
| chr5:112813628 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.835-1867G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813628 | |||||||
| chr5:112813752 | T | TA | 23 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(20): Show |
23 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-1730dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112813752 | ||||||
| chr5:112813752 | T | TAA | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-1731_835-1730d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112813752 | ||||||
| chr5:112813779 | A | C | 16 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.835-1716A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813779 | |||||||
| chr5:112813828 | T | C | 1 | a0001c0003t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.835-1667T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813828 | |||||||
| chr5:112813878 | C | T | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.835-1617C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813878 | |||||||
| chr5:112813973 | T | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-1522T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813973 | |||||||
| chr5:112814060 | T | C | 229 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(226): Show |
231 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(228): Show |
intron_variant | MODIFIER | c.835-1435T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814060 | |||||||
| chr5:112814230 | A | G | 91 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(88): Show |
93 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.835-1265A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814230 | |||||||
| chr5:112814245 | A | G | 1 | a0001c0003t0002g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.835-1250A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814245 | |||||||
| chr5:112814272 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0247 |
2 | NA18981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.835-1223C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814272 | |||||||
| chr5:112814289 | G | A | 1 | a0001c0003t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.835-1206G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814289 | |||||||
| chr5:112814352 | A | G | 16 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.835-1143A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814352 | |||||||
| chr5:112814372 | A | G | 1 | a0002c0004t0002g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835-1123A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814372 | |||||||
| chr5:112814452 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.835-1043T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814452 | |||||||
| chr5:112814546 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.835-949T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814546 | |||||||
| chr5:112814549 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.835-946A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814549 | |||||||
| chr5:112814578 | A | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.835-917A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814578 | |||||||
| chr5:112814630 | C | G | 7 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(4): Show |
7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.835-865C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814630 | |||||||
| chr5:112814843 | G | A | 5 | a0001c0002t0003g0165 a0001c0002t0003g0174 a0001c0002t0003g0175 others(2): Show |
5 | HG00609.hp1 HG02129.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.835-652G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814843 | |||||||
| chr5:112814876 | T | C | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-619T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814876 | |||||||
| chr5:112814928 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.835-567A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814928 | |||||||
| chr5:112815043 | G | C | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-452G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815043 | |||||||
| chr5:112815184 | T | G | 1 | a0002c0020t0012g0054 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.835-311T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815184 | |||||||
| chr5:112815188 | C | T | 1 | a0001c0003t0006g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.835-307C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815188 | |||||||
| chr5:112815236 | A | T | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-259A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815236 | |||||||
| chr5:112815471 | A | T | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.835-24A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815471 | |||||||
| chr5:112815476 | T | C | 1 | a0006c0012t0002g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.835-19T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815476 | |||||||
| chr5:112815822 | G | C | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.933+229G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112815822 | |||||||
| chr5:112815854 | G | T | 174 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(171): Show |
176 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.933+261G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112815854 | |||||||
| chr5:112816077 | C | T | 1 | a0001c0003t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.933+484C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816077 | |||||||
| chr5:112816314 | A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.933+721A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816314 | |||||||
| chr5:112816436 | T | C | 1 | a0007c0023t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.933+843T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816436 | |||||||
| chr5:112816509 | T | G | 40 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(37): Show |
40 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.933+916T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816509 | |||||||
| chr5:112816529 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.933+936C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816529 | |||||||
| chr5:112816652 | G | T | 12 | a0001c0003t0002g0138 a0001c0003t0002g0151 a0001c0003t0006g0140 others(9): Show |
12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+1059G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816652 | |||||||
| chr5:112816697 | G | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.933+1104G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816697 | |||||||
| chr5:112816761 | C | G | 2 | a0001c0002t0005g0115 a0001c0002t0009g0131 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.933+1168C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816761 | |||||||
| chr5:112816825 | C | G | 5 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+1232C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816825 | |||||||
| chr5:112816864 | T | TTTTA | 7 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(4): Show |
7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+1287_933+1290d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr5 | 112816864 | ||||||
| chr5:112816952 | C | T | 173 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(170): Show |
175 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(172): Show |
intron_variant | MODIFIER | c.933+1359C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816952 | |||||||
| chr5:112817133 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.933+1540G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817133 | |||||||
| chr5:112817136 | C | A | 1 | a0001c0002t0003g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.933+1543C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817136 | |||||||
| chr5:112817169 | C | G | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.933+1576C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817169 | |||||||
| chr5:112817170 | C | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.933+1577C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817170 | |||||||
| chr5:112817223 | C | T | 61 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(58): Show |
63 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.933+1630C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817223 | |||||||
| chr5:112817334 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.934-1632T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817334 | |||||||
| chr5:112817422 | C | T | 192 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(189): Show |
194 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(191): Show |
intron_variant | MODIFIER | c.934-1544C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817422 | |||||||
| chr5:112817435 | C | T | 7 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-1531C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817435 | |||||||
| chr5:112817513 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.934-1453A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817513 | |||||||
| chr5:112817570 | C | T | 1 | a0002c0004t0002g0042 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.934-1396C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817570 | |||||||
| chr5:112817656 | T | G | 13 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(10): Show |
13 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.934-1310T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817656 | |||||||
| chr5:112817686 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.934-1280A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817686 | |||||||
| chr5:112817798 | A | G | 216 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(213): Show |
218 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.934-1168A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817798 | |||||||
| chr5:112817831 | C | G | 14 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(11): Show |
14 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-1135C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817831 | |||||||
| chr5:112817876 | T | G | 1 | a0001c0003t0002g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.934-1090T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817876 | |||||||
| chr5:112817940 | A | G | 1 | a0002c0004t0002g0014 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.934-1026A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817940 | |||||||
| chr5:112817966 | A | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.934-1000A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817966 | |||||||
| chr5:112817968 | C | T | 192 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(189): Show |
194 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(191): Show |
intron_variant | MODIFIER | c.934-998C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817968 | |||||||
| chr5:112818025 | T | C | 2 | a0001c0002t0005g0115 a0001c0002t0009g0131 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.934-941T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818025 | |||||||
| chr5:112818060 | T | C | 43 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(40): Show |
45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.934-906T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818060 | |||||||
| chr5:112818164 | C | A | 3 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0016t0001g0244 |
3 | HG02523.hp2 NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.934-802C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818164 | |||||||
| chr5:112818167 | T | C | 1 | a0001c0005t0005g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.934-799T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818167 | |||||||
| chr5:112818200 | A | G | 1 | a0001c0002t0003g0182 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.934-766A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818200 | |||||||
| chr5:112818299 | C | G | 212 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(209): Show |
214 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(211): Show |
intron_variant | MODIFIER | c.934-667C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818299 | |||||||
| chr5:112818362 | G | A | 1 | a0002c0004t0002g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.934-604G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818362 | |||||||
| chr5:112818454 | ATAT | A | 192 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(189): Show |
194 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(191): Show |
intron_variant | MODIFIER | c.934-508_934-506del others(3): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr5 | 112818454 | ||||||
| chr5:112818606 | T | G | 195 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(192): Show |
197 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(194): Show |
intron_variant | MODIFIER | c.934-360T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818606 | |||||||
| chr5:112818688 | G | C | 1 | a0001c0003t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.934-278G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818688 | |||||||
| chr5:112818747 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0283 |
3 | HG00673.hp1 NA19011.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.934-219A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818747 | |||||||
| chr5:112818833 | TG | T | 177 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(174): Show |
179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.934-132delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818833 | |||||||
| chr5:112818834 | G | T | 39 | a0001c0001t0001g0241 a0001c0001t0001g0247 a0001c0001t0001g0254 others(36): Show |
39 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.934-132G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818834 | |||||||
| chr5:112818847 | C | CG | 97 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(94): Show |
97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.934-111dupG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr5 | 112818847 | ||||||
| chr5:112818874 | G | C | 19 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(16): Show |
19 | HG00741.hp2 HG01358.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.934-92G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818874 | |||||||
| chr5:112819371 | G | A | 1 | a0002c0004t0002g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1312+27G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819371 | |||||||
| chr5:112819480 | A | G | 7 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(4): Show |
7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312+136A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819480 | |||||||
| chr5:112819507 | C | G | 5 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0163 others(2): Show |
5 | HG02071.hp1 NA18612.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312+163C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819507 | |||||||
| chr5:112819545 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1312+201A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819545 | |||||||
| chr5:112819721 | A | C | 2 | a0001c0003t0002g0110 a0001c0003t0002g0111 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1312+377A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819721 | |||||||
| chr5:112819805 | T | A | 1 | a0001c0002t0003g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1312+461T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819805 | |||||||
| chr5:112819807 | C | G | 212 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(209): Show |
214 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(211): Show |
intron_variant | MODIFIER | c.1312+463C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819807 | |||||||
| chr5:112819893 | C | T | 7 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(4): Show |
7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312+549C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819893 | |||||||
| chr5:112820063 | C | T | 29 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(26): Show |
29 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1312+719C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820063 | |||||||
| chr5:112820096 | G | C | 196 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(193): Show |
198 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(195): Show |
intron_variant | MODIFIER | c.1312+752G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820096 | |||||||
| chr5:112820182 | G | GAC | 43 | a0001c0001t0001g0221 a0001c0001t0001g0229 a0001c0001t0001g0232 others(40): Show |
43 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1312+871_1312+872d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | ||||||
| chr5:112820182 | G | GACAC | 7 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 others(4): Show |
7 | HG01081.hp1 HG01106.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+869_1312+872d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | ||||||
| chr5:112820182 | GAC | G | 10 | a0001c0001t0001g0075 a0001c0001t0001g0236 a0001c0002t0003g0161 others(7): Show |
10 | HG01496.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312+871_1312+872d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | ||||||
| chr5:112820182 | GACAC | G | 37 | a0001c0001t0001g0246 a0001c0002t0004g0019 a0001c0002t0004g0020 others(34): Show |
37 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1312+869_1312+872d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | ||||||
| chr5:112820182 | GACACAC | G | 38 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0074 others(35): Show |
40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1312+867_1312+872d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | ||||||
| chr5:112820321 | A | G | 3 | a0001c0002t0003g0176 a0001c0002t0003g0177 a0001c0002t0003g0182 |
3 | HG03471.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1312+977A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820321 | |||||||
| chr5:112820425 | G | A | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+1081G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820425 | |||||||
| chr5:112820583 | T | G | 5 | a0001c0002t0003g0001 a0001c0002t0003g0153 a0001c0002t0003g0154 others(2): Show |
6 | HG00408.hp1 HG02155.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312+1239T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820583 | |||||||
| chr5:112820604 | T | C | 1 | a0001c0003t0002g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1312+1260T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820604 | |||||||
| chr5:112820620 | C | T | 1 | a0001c0019t0002g0079 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1312+1276C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820620 | |||||||
| chr5:112820842 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1313-1054T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820842 | |||||||
| chr5:112820937 | C | T | 6 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-959C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820937 | |||||||
| chr5:112820974 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0245 |
2 | NA18950.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1313-922A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820974 | |||||||
| chr5:112820979 | A | T | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1313-917A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820979 | |||||||
| chr5:112820995 | C | A | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1313-901C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820995 | |||||||
| chr5:112821030 | A | AT | 29 | a0001c0001t0001g0122 a0001c0001t0001g0200 a0001c0001t0001g0247 others(26): Show |
29 | HG00741.hp2 HG01358.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.1313-846dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112821030 | ||||||
| chr5:112821030 | AT | A | 15 | a0001c0001t0001g0199 a0001c0001t0001g0245 a0001c0001t0001g0252 others(12): Show |
15 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1313-846delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112821030 | ||||||
| chr5:112821099 | G | A | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1313-797G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821099 | |||||||
| chr5:112821166 | G | C | 76 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0074 others(73): Show |
78 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1313-730G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821166 | |||||||
| chr5:112821234 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1313-662G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821234 | |||||||
| chr5:112821242 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1313-654G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821242 | |||||||
| chr5:112821400 | C | T | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1313-496C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821400 | |||||||
| chr5:112821401 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1313-495G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821401 | |||||||
| chr5:112821504 | G | GT | 20 | a0001c0002t0004g0022 a0001c0002t0004g0023 a0001c0002t0004g0024 others(17): Show |
20 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1313-382dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112821504 | ||||||
| chr5:112821716 | T | A | 1 | a0002c0004t0002g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1313-180T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821716 | |||||||
| chr5:112822130 | G | A | 1 | a0001c0005t0011g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1408+139G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822130 | |||||||
| chr5:112822427 | A | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408+436A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822427 | |||||||
| chr5:112822676 | G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1408+685G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822676 | |||||||
| chr5:112822734 | G | A | 185 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(182): Show |
187 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(184): Show |
intron_variant | MODIFIER | c.1408+743G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822734 | |||||||
| chr5:112822783 | A | T | 14 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(11): Show |
14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+792A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822783 | |||||||
| chr5:112823052 | A | T | 15 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(12): Show |
15 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1408+1061A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823052 | |||||||
| chr5:112823321 | C | T | 1 | a0002c0004t0002g0090 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1408+1330C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823321 | |||||||
| chr5:112823376 | G | A | 1 | a0001c0003t0006g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1408+1385G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823376 | |||||||
| chr5:112823519 | T | G | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+1528T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823519 | |||||||
| chr5:112823593 | A | G | 11 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(8): Show |
11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408+1602A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823593 | |||||||
| chr5:112823663 | A | G | 32 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(29): Show |
32 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1408+1672A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823663 | |||||||
| chr5:112823688 | A | G | 288 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(285): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1408+1697A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823688 | |||||||
| chr5:112823711 | T | C | 5 | a0001c0002t0003g0001 a0001c0002t0003g0153 a0001c0002t0003g0154 others(2): Show |
6 | HG00408.hp1 HG02155.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+1720T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823711 | |||||||
| chr5:112823773 | A | G | 99 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(96): Show |
99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.1408+1782A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823773 | |||||||
| chr5:112823848 | A | C | 17 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(14): Show |
17 | HG01081.hp1 HG01106.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1408+1857A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823848 | |||||||
| chr5:112823865 | A | G | 236 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(233): Show |
238 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(235): Show |
intron_variant | MODIFIER | c.1408+1874A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823865 | |||||||
| chr5:112823939 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1408+1948C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823939 | |||||||
| chr5:112823986 | A | T | 1 | a0001c0002t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1408+1995A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823986 | |||||||
| chr5:112824207 | G | A | 1 | a0014c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1408+2216G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824207 | |||||||
| chr5:112824208 | C | A | 1 | a0014c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1408+2217C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824208 | |||||||
| chr5:112824277 | G | A | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1408+2286G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824277 | |||||||
| chr5:112824728 | C | T | 1 | a0001c0002t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1409-2380C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824728 | |||||||
| chr5:112824745 | CTCATTAG others(14): Show |
C | 177 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(174): Show |
179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1409-2360_1409-234 others(25): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112824745 | ||||||
| chr5:112824883 | T | C | 14 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(11): Show |
14 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-2225T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824883 | |||||||
| chr5:112824898 | T | A | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1409-2210T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824898 | |||||||
| chr5:112824912 | T | C | 1 | a0001c0002t0003g0162 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1409-2196T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824912 | |||||||
| chr5:112825027 | A | G | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-2081A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825027 | |||||||
| chr5:112825095 | C | T | 1 | a0004c0009t0002g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1409-2013C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825095 | |||||||
| chr5:112825314 | G | A | 4 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0167 others(1): Show |
4 | HG02071.hp1 NA18612.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-1794G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825314 | |||||||
| chr5:112825430 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1409-1678C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825430 | |||||||
| chr5:112825617 | C | T | 62 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(59): Show |
64 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1409-1491C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825617 | |||||||
| chr5:112825622 | C | T | 1 | a0001c0003t0006g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1409-1486C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825622 | |||||||
| chr5:112825650 | G | A | 6 | a0001c0001t0001g0201 a0001c0001t0001g0211 a0001c0003t0002g0108 others(3): Show |
6 | HG02818.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-1458G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825650 | |||||||
| chr5:112825693 | A | G | 1 | a0002c0020t0012g0054 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1409-1415A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825693 | |||||||
| chr5:112825772 | C | A | 98 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.1409-1336C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825772 | |||||||
| chr5:112825864 | C | T | 2 | a0001c0002t0005g0128 a0001c0003t0002g0045 |
2 | HG02257.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1409-1244C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825864 | |||||||
| chr5:112826082 | C | G | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-1026C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826082 | |||||||
| chr5:112826142 | TC | T | 42 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(39): Show |
44 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1409-965delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826142 | |||||||
| chr5:112826208 | T | C | 2 | a0003c0006t0001g0277 a0003c0006t0001g0278 |
2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1409-900T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826208 | |||||||
| chr5:112826222 | G | T | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1409-886G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826222 | |||||||
| chr5:112826586 | T | TA | 6 | a0001c0002t0003g0156 a0001c0002t0003g0159 a0001c0002t0003g0186 others(3): Show |
6 | HG00408.hp2 HG01109.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-507dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826586 | ||||||
| chr5:112826586 | TAA | T | 27 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(24): Show |
27 | HG00741.hp2 HG01496.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.1409-508_1409-507d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826586 | ||||||
| chr5:112826599 | AAAC | A | 13 | a0001c0002t0003g0176 a0001c0002t0003g0177 a0001c0002t0003g0182 others(10): Show |
13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1409-506_1409-504d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826599 | ||||||
| chr5:112826600 | AAC | A | 27 | a0001c0001t0001g0202 a0001c0001t0001g0260 a0001c0002t0004g0019 others(24): Show |
27 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1409-506_1409-505d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826600 | ||||||
| chr5:112826601 | AC | A | 100 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(97): Show |
100 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.1409-506delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826601 | |||||||
| chr5:112826602 | C | A | 52 | a0001c0001t0001g0223 a0001c0001t0001g0233 a0001c0001t0001g0234 others(49): Show |
54 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1409-506C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826602 | |||||||
| chr5:112826716 | A | G | 112 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(109): Show |
112 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.1409-392A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826716 | |||||||
| chr5:112827394 | T | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1548+147T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/15 | chr5 | 112827394 | |||||||
| chr5:112827537 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1548+290A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/15 | chr5 | 112827537 | |||||||
| chr5:112827541 | G | GT | 187 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(184): Show |
189 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(186): Show |
intron_variant | MODIFIER | c.1548+297dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr5 | 112827541 | ||||||
| chr5:112828160 | C | T | 1 | a0001c0015t0002g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1626+154C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828160 | |||||||
| chr5:112828161 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1626+155G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828161 | |||||||
| chr5:112828292 | G | A | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+286G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828292 | |||||||
| chr5:112828305 | C | G | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+299C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828305 | |||||||
| chr5:112828457 | T | A | 1 | a0004c0009t0002g0103 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1627-399T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828457 | |||||||
| chr5:112828457 | TA | T | 191 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(188): Show |
193 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(190): Show |
intron_variant | MODIFIER | c.1627-382delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr5 | 112828457 | ||||||
| chr5:112828516 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1627-340G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828516 | |||||||
| chr5:112828541 | C | T | 184 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(181): Show |
186 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(183): Show |
intron_variant | MODIFIER | c.1627-315C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828541 | |||||||
| chr5:112828547 | G | T | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-309G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828547 | |||||||
| chr5:112828763 | A | C | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-93A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828763 | |||||||
| chr5:112828830 | T | A | 1 | a0001c0003t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1627-26T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828830 | |||||||
| chr5:112829050 | A | G | 3 | a0001c0003t0002g0015 a0002c0004t0002g0016 a0008c0032t0002g0017 |
3 | HG00323.hp2 HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1743+78A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829050 | |||||||
| chr5:112829140 | T | G | 1 | a0001c0003t0002g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1743+168T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829140 | |||||||
| chr5:112829165 | G | A | 98 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(95): Show |
98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.1743+193G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829165 | |||||||
| chr5:112829209 | G | C | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+237G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829209 | |||||||
| chr5:112829239 | A | G | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+267A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829239 | |||||||
| chr5:112829354 | C | T | 13 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(10): Show |
13 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1743+382C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829354 | |||||||
| chr5:112829466 | C | A | 3 | a0001c0002t0005g0126 a0001c0002t0005g0127 a0001c0002t0005g0128 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1743+494C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829466 | |||||||
| chr5:112829490 | C | T | 1 | a0001c0002t0003g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1743+518C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829490 | |||||||
| chr5:112829678 | C | T | 5 | a0001c0002t0003g0165 a0001c0002t0003g0174 a0001c0002t0003g0175 others(2): Show |
5 | HG00609.hp1 HG02129.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+706C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829678 | |||||||
| chr5:112829741 | G | A | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+769G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829741 | |||||||
| chr5:112829897 | A | G | 1 | a0001c0029t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1743+925A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829897 | |||||||
| chr5:112829931 | C | T | 4 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+959C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829931 | |||||||
| chr5:112830047 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1743+1075A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830047 | |||||||
| chr5:112830142 | CT | C | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+1172delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112830142 | ||||||
| chr5:112830292 | G | A | 38 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0074 others(35): Show |
40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1743+1320G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830292 | |||||||
| chr5:112830334 | G | A | 4 | a0001c0003t0002g0108 a0001c0003t0002g0110 a0001c0003t0002g0111 others(1): Show |
4 | HG02818.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+1362G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830334 | |||||||
| chr5:112830347 | AACT | A | 176 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(173): Show |
178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.1743+1378_1743+138 others(7): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112830347 | ||||||
| chr5:112830523 | A | G | 4 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+1551A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830523 | |||||||
| chr5:112830589 | TACAC | T | 15 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(12): Show |
15 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1743+1621_1743+162 others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112830589 | ||||||
| chr5:112830874 | G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+1902G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830874 | |||||||
| chr5:112831053 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1743+2081G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831053 | |||||||
| chr5:112831054 | C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+2082C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831054 | |||||||
| chr5:112831113 | A | AT | 14 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(11): Show |
14 | HG02257.hp1 HG02683.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1743+2155dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112831113 | ||||||
| chr5:112831131 | A | G | 1 | a0001c0002t0003g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1743+2159A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831131 | |||||||
| chr5:112831165 | G | A | 94 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(91): Show |
94 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.1743+2193G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831165 | |||||||
| chr5:112831178 | G | A | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+2206G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831178 | |||||||
| chr5:112831198 | T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+2226T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831198 | |||||||
| chr5:112831258 | G | A | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1743+2286G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831258 | |||||||
| chr5:112831328 | T | A | 2 | a0003c0006t0001g0277 a0003c0006t0001g0278 |
2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1743+2356T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831328 | |||||||
| chr5:112831433 | T | G | 204 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(201): Show |
206 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(203): Show |
intron_variant | MODIFIER | c.1743+2461T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831433 | |||||||
| chr5:112831586 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0274 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1743+2614A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831586 | |||||||
| chr5:112831611 | T | C | 4 | a0001c0003t0002g0053 a0001c0003t0002g0056 a0001c0003t0002g0057 others(1): Show |
4 | HG01106.hp1 HG01169.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1743+2639T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831611 | |||||||
| chr5:112831782 | A | G | 1 | a0001c0003t0002g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1743+2810A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831782 | |||||||
| chr5:112831840 | T | C | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+2868T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831840 | |||||||
| chr5:112831890 | T | C | 96 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(93): Show |
96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1743+2918T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831890 | |||||||
| chr5:112832124 | C | T | 176 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(173): Show |
178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.1744-2827C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832124 | |||||||
| chr5:112832217 | A | G | 1 | a0001c0003t0002g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1744-2734A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832217 | |||||||
| chr5:112832224 | G | A | 37 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(34): Show |
37 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1744-2727G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832224 | |||||||
| chr5:112832244 | C | G | 177 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(174): Show |
179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1744-2707C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832244 | |||||||
| chr5:112832272 | T | C | 1 | a0001c0003t0002g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1744-2679T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832272 | |||||||
| chr5:112832368 | A | G | 176 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(173): Show |
178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.1744-2583A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832368 | |||||||
| chr5:112832409 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1744-2542C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832409 | |||||||
| chr5:112832433 | G | C | 176 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(173): Show |
178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.1744-2518G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832433 | |||||||
| chr5:112832446 | T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1744-2505T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832446 | |||||||
| chr5:112832452 | C | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1744-2499C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832452 | |||||||
| chr5:112832576 | T | C | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744-2375T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832576 | |||||||
| chr5:112832622 | T | C | 1 | a0001c0002t0003g0158 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1744-2329T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832622 | |||||||
| chr5:112832645 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1744-2306C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832645 | |||||||
| chr5:112832708 | C | T | 2 | a0001c0002t0003g0159 a0001c0002t0003g0160 |
2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1744-2243C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832708 | |||||||
| chr5:112832754 | C | T | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1744-2197C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832754 | |||||||
| chr5:112832875 | T | A | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1744-2076T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832875 | |||||||
| chr5:112833029 | GT | G | 175 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(172): Show |
177 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(174): Show |
intron_variant | MODIFIER | c.1744-1910delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833029 | ||||||
| chr5:112833041 | T | G | 16 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1744-1910T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833041 | |||||||
| chr5:112833062 | T | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0211 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1744-1889T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833062 | |||||||
| chr5:112833123 | C | G | 2 | a0001c0010t0007g0132 a0001c0014t0007g0133 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1744-1828C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833123 | |||||||
| chr5:112833153 | A | G | 12 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1744-1798A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833153 | |||||||
| chr5:112833180 | A | AT | 9 | a0001c0003t0002g0149 a0001c0003t0006g0140 a0001c0003t0006g0141 others(6): Show |
9 | HG00741.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1744-1751dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833180 | ||||||
| chr5:112833180 | AT | A | 175 | a0001c0001t0001g0075 a0001c0001t0001g0195 a0001c0001t0001g0196 others(172): Show |
177 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1744-1751delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833180 | ||||||
| chr5:112833180 | ATT | A | 8 | a0001c0001t0001g0194 a0001c0001t0001g0206 a0001c0001t0001g0212 others(5): Show |
8 | HG01070.hp1 HG01070.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744-1752_1744-175 others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833180 | ||||||
| chr5:112833196 | T | G | 8 | a0001c0005t0005g0005 a0001c0005t0005g0006 a0001c0005t0005g0008 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744-1755T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833196 | |||||||
| chr5:112833207 | G | A | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-1744G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833207 | |||||||
| chr5:112833342 | C | T | 2 | a0001c0003t0002g0032 a0001c0003t0002g0033 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1744-1609C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833342 | |||||||
| chr5:112833374 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1744-1577G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833374 | |||||||
| chr5:112833393 | G | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1744-1558G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833393 | |||||||
| chr5:112833423 | C | A | 4 | a0001c0001t0001g0122 a0001c0001t0004g0121 a0001c0001t0004g0123 others(1): Show |
4 | HG01358.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-1528C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833423 | |||||||
| chr5:112833434 | G | GC | 12 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1744-1513dupC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833434 | ||||||
| chr5:112833439 | T | C | 176 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(173): Show |
178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.1744-1512T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833439 | |||||||
| chr5:112833479 | C | T | 3 | a0001c0010t0007g0094 a0001c0010t0007g0132 a0001c0014t0007g0133 |
3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1744-1472C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833479 | |||||||
| chr5:112833481 | G | A | 4 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-1470G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833481 | |||||||
| chr5:112833828 | T | A | 214 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(211): Show |
216 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(213): Show |
intron_variant | MODIFIER | c.1744-1123T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833828 | |||||||
| chr5:112833927 | A | G | 64 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(61): Show |
66 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1744-1024A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833927 | |||||||
| chr5:112834105 | A | AT | 24 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(21): Show |
24 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1744-836dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112834105 | ||||||
| chr5:112834193 | C | G | 43 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(40): Show |
45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1744-758C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834193 | |||||||
| chr5:112834200 | A | G | 2 | a0001c0010t0007g0132 a0001c0014t0007g0133 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1744-751A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834200 | |||||||
| chr5:112834238 | C | CT | 7 | a0001c0008t0002g0130 a0001c0030t0002g0129 a0002c0004t0002g0040 others(4): Show |
7 | HG01891.hp1 HG03486.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1744-691dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112834238 | ||||||
| chr5:112834259 | TTA | T | 10 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0001g0209 others(7): Show |
10 | HG01070.hp1 HG01243.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1744-691_1744-690d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834259 | |||||||
| chr5:112834260 | TA | T | 160 | a0001c0001t0001g0075 a0001c0001t0001g0195 a0001c0001t0001g0196 others(157): Show |
162 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.1744-686delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112834260 | ||||||
| chr5:112834261 | A | T | 7 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0229 others(4): Show |
7 | HG02145.hp2 HG02602.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1744-690A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834261 | |||||||
| chr5:112834262 | A | T | 4 | a0001c0002t0003g0001 a0001c0002t0005g0115 a0001c0010t0007g0132 others(1): Show |
5 | HG00408.hp1 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-689A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834262 | |||||||
| chr5:112834268 | G | T | 1 | a0001c0010t0007g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1744-683G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834268 | |||||||
| chr5:112834345 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1744-606G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834345 | |||||||
| chr5:112834588 | T | A | 24 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0074 others(21): Show |
26 | HG00408.hp1 HG00609.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1744-363T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834588 | |||||||
| chr5:112834661 | G | A | 211 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(208): Show |
213 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(210): Show |
intron_variant | MODIFIER | c.1744-290G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834661 | |||||||
| chr5:112834793 | A | G | 9 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1744-158A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834793 | |||||||
| chr5:112834840 | G | A | 2 | a0001c0001t0004g0261 a0001c0001t0004g0262 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1744-111G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834840 | |||||||
| chr5:112835173 | T | C | 14 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(11): Show |
14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1958+8T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835173 | |||||||
| chr5:112835198 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0223 |
2 | NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1958+33A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835198 | |||||||
| chr5:112835219 | A | C | 12 | a0001c0002t0005g0115 a0001c0002t0005g0126 a0001c0002t0005g0127 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1958+54A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835219 | |||||||
| chr5:112835274 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0240 a0001c0001t0001g0250 |
3 | HG04184.hp1 NA18954.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1958+109A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835274 | |||||||
| chr5:112835400 | A | G | 43 | a0001c0001t0001g0259 a0001c0002t0001g0286 a0001c0002t0001g0287 others(40): Show |
45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1958+235A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835400 | |||||||
| chr5:112835503 | C | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1958+338C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835503 | |||||||
| chr5:112835572 | A | AT | 79 | a0001c0001t0001g0122 a0001c0001t0001g0259 a0001c0001t0004g0116 others(76): Show |
81 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1958+425dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112835572 | ||||||
| chr5:112835572 | A | ATT | 15 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1958+424_1958+425d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112835572 | ||||||
| chr5:112835572 | A | T | 1 | a0001c0002t0003g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1958+407A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835572 | |||||||
| chr5:112835572 | AT | A | 111 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(108): Show |
111 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.1958+425delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112835572 | ||||||
| chr5:112835747 | A | G | 1 | a0001c0002t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1958+582A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835747 | |||||||
| chr5:112835748 | T | C | 1 | a0001c0031t0002g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1958+583T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835748 | |||||||
| chr5:112835863 | G | A | 8 | a0001c0002t0004g0188 a0001c0002t0004g0189 a0001c0002t0004g0190 others(5): Show |
8 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1958+698G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835863 | |||||||
| chr5:112836009 | C | CT | 6 | a0001c0003t0002g0039 a0001c0003t0002g0060 a0001c0003t0002g0112 others(3): Show |
6 | HG01346.hp1 HG02293.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+870dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CT | C | 43 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0074 others(40): Show |
45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1958+870delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTT | C | 14 | a0001c0002t0003g0161 a0001c0002t0004g0019 a0001c0002t0004g0020 others(11): Show |
14 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+869_1958+870d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTTT | C | 11 | a0001c0001t0001g0122 a0001c0001t0004g0116 a0001c0001t0004g0117 others(8): Show |
11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1958+868_1958+870d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTTTT | C | 9 | a0001c0002t0005g0127 a0001c0002t0005g0128 a0001c0005t0005g0005 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1958+867_1958+870d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTTTTTT | C | 7 | a0001c0003t0002g0134 a0001c0003t0002g0136 a0001c0003t0002g0137 others(4): Show |
7 | HG01496.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1958+865_1958+870d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTTTTTTT | C | 27 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(24): Show |
27 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.1958+864_1958+870d others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTTTTTTT others(2): Show |
C | 14 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0209 others(11): Show |
14 | HG01071.hp1 HG01975.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+862_1958+870d others(11): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836009 | CTTTTTTT others(3): Show |
C | 81 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(78): Show |
81 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1958+861_1958+870d others(12): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | ||||||
| chr5:112836025 | TTTTTTTT others(4): Show |
T | 1 | a0001c0001t0001g0220 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1958+863_1958+873d others(13): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836025 | ||||||
| chr5:112836037 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1958+872T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836037 | |||||||
| chr5:112836064 | G | A | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0274 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958+899G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836064 | |||||||
| chr5:112836087 | C | T | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1958+922C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836087 | |||||||
| chr5:112836165 | T | C | 1 | a0001c0008t0002g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1958+1000T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TC | 18 | a0001c0002t0005g0115 a0001c0003t0002g0039 a0001c0003t0002g0057 others(15): Show |
18 | HG01106.hp1 HG01109.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1958+1014dupC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCC | 13 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0025 others(10): Show |
13 | HG01884.hp2 HG02155.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1958+1010_1958+101 others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(3): Show |
1 | a0001c0003t0002g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1958+1005_1958+101 others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(4): Show |
1 | a0001c0002t0004g0190 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1958+1004_1958+101 others(15): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(9): Show |
1 | a0001c0007t0004g0119 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1958+1013_1958+101 others(20): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(12): Show |
1 | a0001c0001t0004g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1958+1013_1958+101 others(23): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(8): Show |
1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1958+1012_1958+101 others(19): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(9): Show |
3 | a0001c0001t0001g0122 a0001c0007t0004g0118 a0001c0007t0004g0120 |
3 | HG01081.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1958+1012_1958+101 others(20): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(11): Show |
1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1958+1012_1958+101 others(22): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TCCCCCCC others(12): Show |
1 | a0001c0001t0004g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1958+1012_1958+101 others(23): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836165 | T | TTCCCC | 4 | a0001c0001t0001g0214 a0001c0001t0001g0223 a0001c0001t0001g0257 others(1): Show |
4 | HG01358.hp2 NA19009.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCC | 10 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0242 others(7): Show |
10 | HG01346.hp2 HG01981.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC | 34 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0001t0001g0203 others(31): Show |
34 | HG00673.hp2 HG00741.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(11): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC others(1): Show |
21 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0198 others(18): Show |
21 | HG00609.hp2 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(12): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC others(2): Show |
14 | a0001c0001t0001g0075 a0001c0001t0001g0217 a0001c0001t0001g0221 others(11): Show |
14 | HG00642.hp2 HG00673.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(13): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC others(3): Show |
4 | a0001c0001t0001g0205 a0001c0001t0001g0224 a0001c0001t0001g0281 others(1): Show |
4 | HG03927.hp2 NA18954.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC others(4): Show |
2 | a0001c0001t0001g0212 a0001c0016t0001g0244 |
2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(15): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC others(5): Show |
1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1958+1000_1958+100 others(16): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | T | TTCCCCCC others(6): Show |
1 | a0001c0001t0001g0251 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1958+1000_1958+100 others(17): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | |||||||
| chr5:112836165 | TC | T | 40 | a0001c0001t0004g0116 a0001c0002t0008g0184 a0001c0002t0008g0185 others(37): Show |
40 | HG00323.hp2 HG00639.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1958+1014delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | ||||||
| chr5:112836166 | C | T | 1 | a0003c0006t0001g0263 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1958+1001C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836166 | |||||||
| chr5:112836172 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1958+1007C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836172 | |||||||
| chr5:112836173 | C | T | 6 | a0002c0004t0002g0087 a0002c0004t0002g0095 a0002c0004t0002g0096 others(3): Show |
6 | NA18957.hp1 NA18963.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+1008C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836173 | |||||||
| chr5:112836174 | C | G | 3 | a0001c0003t0002g0149 a0005c0013t0002g0148 a0005c0013t0002g0150 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1958+1009C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836174 | |||||||
| chr5:112836177 | C | A | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1958+1012C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836177 | |||||||
| chr5:112836177 | C | CT | 27 | a0001c0002t0001g0287 a0001c0002t0001g0288 a0001c0002t0001g0289 others(24): Show |
29 | HG00408.hp1 HG00609.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1958+1012_1958+101 others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836177 | |||||||
| chr5:112836177 | C | G | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1958+1012C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836177 | |||||||
| chr5:112836178 | C | CTT | 13 | a0001c0002t0001g0286 a0001c0002t0003g0153 a0001c0002t0003g0157 others(10): Show |
13 | HG01891.hp2 HG02071.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.1958+1013_1958+101 others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836178 | |||||||
| chr5:112836178 | C | T | 27 | a0001c0002t0001g0287 a0001c0002t0001g0288 a0001c0002t0001g0289 others(24): Show |
29 | HG00408.hp1 HG00609.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1958+1013C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836178 | |||||||
| chr5:112836180 | G | A | 95 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0195 others(92): Show |
95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1958+1015G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836180 | |||||||
| chr5:112836186 | G | A | 15 | a0001c0003t0002g0138 a0001c0003t0002g0149 a0001c0003t0002g0151 others(12): Show |
15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1958+1021G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836186 | |||||||
| chr5:112836221 | G | A | 29 | a0001c0003t0002g0004 a0001c0003t0002g0043 a0001c0003t0002g0044 others(26): Show |
29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.1958+1056G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836221 | |||||||
| chr5:112836522 | G | A | 186 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(183): Show |
188 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(185): Show |
intron_variant | MODIFIER | c.1959-1031G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836522 | |||||||
| chr5:112836819 | G | C | 5 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0001g0253 others(2): Show |
5 | HG01981.hp1 HG01993.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1959-734G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836819 | |||||||
| chr5:112837010 | C | T | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1959-543C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837010 | |||||||
| chr5:112837089 | G | T | 186 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(183): Show |
188 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(185): Show |
intron_variant | MODIFIER | c.1959-464G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837089 | |||||||
| chr5:112837103 | C | T | 8 | a0001c0003t0006g0140 a0001c0003t0006g0141 a0001c0003t0006g0142 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1959-450C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837103 | |||||||
| chr5:112837186 | A | G | 1 | a0001c0002t0004g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1959-367A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837186 | |||||||
| chr5:112837233 | T | C | 112 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(109): Show |
112 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.1959-320T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837233 | |||||||
| chr5:112837409 | T | TAGAA | 187 | a0001c0001t0001g0075 a0001c0001t0001g0122 a0001c0001t0001g0194 others(184): Show |
189 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(186): Show |
intron_variant | MODIFIER | c.1959-143_1959-140d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112837409 | ||||||
| chr5:112837424 | T | A | 2 | a0001c0002t0008g0184 a0001c0002t0008g0185 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1959-129T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837424 |