Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 85002 |
| ensemblid | ENSG00000186523.15 |
| hgncid | 28268 |
| symbol | FAM86B1 |
| name | family with sequence similarity 86 member B1 |
| refseq_nuc | NM_001083537.4 |
| refseq_prot | NP_001077006.1 |
| ensembl_nuc | ENST00000448228.7 |
| ensembl_prot | ENSP00000407067.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 12182106 |
| end | 12194082 |
| strand | - |
| ver | v1.2 |
| region | chr8:12182106-12194082 |
| region5000 | chr8:12177106-12199082 |
| regionname0 | FAM86B1_chr8_12182106_12194082 |
| regionname5000 | FAM86B1_chr8_12177106_12199082 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 296 | 66 | 5 | 11 | 41 | 2 | 5 | 37 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0002 | 0/0 | 296 | 53 | 0 | 11 | 36 | 2 | 4 | 33 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0003 | 0/0 | 296 | 20 | 0 | 7 | 11 | 1 | 1 | 10 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0004 | 0/0 | 296 | 6 | 0 | 3 | 3 | 0 | 0 | 3 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0005 | 0/0 | 30 | 6 | 5 | 0 | 0 | 0 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MTPEE others(25): Show |
chr8 | 12177106 | 12199082 |
| a0006 | 0/0 | 296 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0007 | 0/0 | 296 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0008 | 0/0 | 296 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0009 | 0/0 | 296 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MTPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0010 | 0/0 | 296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0011 | 0/0 | 71 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MTPEE others(66): Show |
chr8 | 12177106 | 12199082 |
| a0012 | 0/0 | 296 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0013 | 0/0 | 296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0014 | 0/0 | 190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(185): Show |
chr8 | 12177106 | 12199082 |
| a0015 | 0/0 | 296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0016 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0017 | 0/0 | 190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(185): Show |
chr8 | 12177106 | 12199082 |
| a0018 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| a0019 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | MAPEE others(291): Show |
chr8 | 12177106 | 12199082 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 888 | 49 | 4 | 7 | 32 | 0 | 4 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0001c0005 | 0/0 | 888 | 12 | 0 | 2 | 9 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0001c0015 | 0/0 | 888 | 2 | 0 | 0 | 0 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0001c0021 | 0/0 | 888 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0001c0023 | 0/0 | 888 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0001c0024 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0002c0002 | 0/0 | 888 | 31 | 0 | 7 | 20 | 2 | 2 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0002c0003 | 0/0 | 888 | 19 | 0 | 4 | 14 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0002c0017 | 0/0 | 888 | 2 | 0 | 0 | 1 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0002c0026 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0003c0004 | 0/0 | 888 | 17 | 0 | 7 | 8 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0003c0010 | 0/0 | 888 | 3 | 0 | 0 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0004c0006 | 0/0 | 888 | 6 | 0 | 3 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0005c0007 | 0/0 | 888 | 4 | 4 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGAC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0005c0012 | 0/0 | 888 | 2 | 1 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGAC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0006c0008 | 0/0 | 888 | 4 | 0 | 2 | 0 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0007c0009 | 0/0 | 888 | 3 | 3 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0008c0016 | 0/0 | 888 | 2 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0008c0020 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0009c0011 | 0/0 | 888 | 2 | 0 | 2 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGAC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0010c0018 | 0/0 | 888 | 2 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0011c0013 | 0/0 | 888 | 2 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGAC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0012c0014 | 0/0 | 888 | 2 | 0 | 0 | 0 | 2 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0013c0025 | 0/0 | 888 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0014c0022 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0015c0029 | 0/0 | 888 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0016c0019 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0017c0030 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0018c0028 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 | ||
| a0019c0027 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | ATGGC others(883): Show |
chr8 | 12177106 | 12199082 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 2403 | 38 | 0 | 3 | 31 | 0 | 2 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0001c0001t0003 | 0/0 | 2299 | 9 | 3 | 4 | 1 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0001t0012 | 0/0 | 2299 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0001t0013 | 0/0 | 2299 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0005t0002 | 0/0 | 2403 | 8 | 0 | 1 | 6 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0001c0005t0003 | 0/0 | 2299 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0005t0011 | 0/0 | 2299 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0005t0014 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0001c0005t0015 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0001c0015t0006 | 0/0 | 2403 | 2 | 0 | 0 | 0 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0001c0021t0003 | 0/0 | 2299 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0023t0001 | 0/0 | 2299 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0001c0024t0018 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2346): Show |
chr8 | 12177106 | 12199082 |
| a0002c0002t0001 | 0/0 | 2299 | 30 | 0 | 7 | 20 | 2 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0002c0002t0016 | 0/0 | 2299 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0002c0003t0001 | 0/0 | 2299 | 19 | 0 | 4 | 14 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0002c0017t0002 | 0/0 | 2403 | 2 | 0 | 0 | 1 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0002c0026t0003 | 0/0 | 2299 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0003c0004t0001 | 0/0 | 2299 | 17 | 0 | 7 | 8 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0003c0010t0001 | 0/0 | 2299 | 3 | 0 | 0 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0004c0006t0001 | 0/0 | 2299 | 6 | 0 | 3 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0005c0007t0004 | 0/0 | 2370 | 3 | 3 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2365): Show |
chr8 | 12177106 | 12199082 |
| a0005c0007t0009 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CCGCC others(2364): Show |
chr8 | 12177106 | 12199082 |
| a0005c0012t0004 | 0/0 | 2370 | 2 | 1 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2365): Show |
chr8 | 12177106 | 12199082 |
| a0006c0008t0001 | 0/0 | 2299 | 4 | 0 | 2 | 0 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0007c0009t0003 | 0/0 | 2299 | 3 | 3 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0008c0016t0002 | 0/0 | 2403 | 2 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0008c0020t0002 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2398): Show |
chr8 | 12177106 | 12199082 |
| a0009c0011t0005 | 0/0 | 3133 | 2 | 0 | 2 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(3128): Show |
chr8 | 12177106 | 12199082 |
| a0010c0018t0001 | 0/0 | 2299 | 2 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0011c0013t0008 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CCGCC others(2365): Show |
chr8 | 12177106 | 12199082 |
| a0011c0013t0010 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2366): Show |
chr8 | 12177106 | 12199082 |
| a0012c0014t0007 | 0/0 | 2351 | 2 | 0 | 0 | 0 | 2 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2346): Show |
chr8 | 12177106 | 12199082 |
| a0013c0025t0001 | 0/0 | 2299 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0014c0022t0020 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2366): Show |
chr8 | 12177106 | 12199082 |
| a0015c0029t0001 | 0/0 | 2299 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0016c0019t0001 | 0/0 | 2299 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0017c0030t0019 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2366): Show |
chr8 | 12177106 | 12199082 |
| a0018c0028t0001 | 0/0 | 2299 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| a0019c0027t0017 | 0/0 | 2299 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | CTCGC others(2294): Show |
chr8 | 12177106 | 12199082 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0001t0013g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0014g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0005t0015g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0015t0006g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0021t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0023t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0001c0024t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0001 | 0/0 | 12 | 0 | 3 | 8 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0002t0016g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0017t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0017t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0002c0026t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0010t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0010t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0003c0010t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0004c0006t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0004c0006t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0004c0006t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0004c0006t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0004c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0005c0007t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0005c0007t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0005c0007t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0005c0007t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0005c0012t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0005c0012t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0006c0008t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0006c0008t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0006c0008t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0007c0009t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0007c0009t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0007c0009t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0008c0016t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0008c0016t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0008c0020t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0009c0011t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0009c0011t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0010c0018t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0011c0013t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0011c0013t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0012c0014t0007g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0013c0025t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0014c0022t0020g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0015c0029t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0016c0019t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0017c0030t0019g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0018c0028t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| a0019c0027t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0003 | c0004 | t0001 | g0049 | EUR | FIN | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00323 | hp2 | a0001 | c0015 | t0006 | g0013 | EUR | FIN | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | CHS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00642 | hp1 | a0006 | c0008 | t0001 | g0058 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG00642 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0091 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01070 | hp2 | a0009 | c0011 | t0005 | g0027 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01099 | hp1 | a0001 | c0023 | t0001 | g0067 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01106 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0053 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01175 | hp1 | a0001 | c0021 | t0003 | g0121 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01175 | hp2 | a0006 | c0008 | t0001 | g0059 | AMR | PUR | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01257 | hp1 | a0009 | c0011 | t0005 | g0026 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0048 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01346 | hp1 | a0004 | c0006 | t0001 | g0041 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0088 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01433 | hp2 | a0013 | c0025 | t0001 | g0085 | AMR | CLM | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01515 | hp2 | a0001 | c0005 | t0002 | g0104 | EUR | IBS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0077 | EUR | IBS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01516 | hp2 | a0006 | c0008 | t0001 | g0012 | EUR | IBS | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01884 | hp1 | a0014 | c0022 | t0020 | g0132 | AFR | ACB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01884 | hp2 | a0010 | c0018 | t0001 | g0017 | AFR | ACB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01928 | hp1 | a0004 | c0006 | t0001 | g0011 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01934 | hp1 | a0001 | c0005 | t0003 | g0119 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01934 | hp2 | a0003 | c0004 | t0001 | g0002 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01975 | hp2 | a0015 | c0029 | t0001 | g0054 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0039 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0051 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0061 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02148 | hp2 | a0004 | c0006 | t0001 | g0043 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02300 | hp1 | a0001 | c0005 | t0002 | g0070 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02523 | hp1 | a0003 | c0004 | t0001 | g0055 | EAS | KHV | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02523 | hp2 | a0001 | c0005 | t0002 | g0021 | EAS | KHV | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02572 | hp1 | a0007 | c0009 | t0003 | g0124 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02572 | hp2 | a0005 | c0007 | t0004 | g0032 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02717 | hp1 | a0007 | c0009 | t0003 | g0123 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02717 | hp2 | a0005 | c0007 | t0004 | g0031 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0086 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02886 | hp2 | a0001 | c0024 | t0018 | g0035 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03041 | hp1 | a0016 | c0019 | t0001 | g0034 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03041 | hp2 | a0017 | c0030 | t0019 | g0134 | AFR | GWD | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03139 | hp1 | a0008 | c0016 | t0002 | g0069 | AFR | ESN | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03139 | hp2 | a0005 | c0012 | t0004 | g0030 | AFR | ESN | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03209 | hp1 | a0011 | c0013 | t0010 | g0033 | AFR | MSL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03209 | hp2 | a0008 | c0020 | t0002 | g0068 | AFR | MSL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03490 | hp2 | a0001 | c0015 | t0006 | g0013 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03491 | hp1 | a0002 | c0017 | t0002 | g0038 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03491 | hp2 | a0005 | c0012 | t0004 | g0029 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03654 | hp2 | a0002 | c0002 | t0016 | g0075 | SAS | PJL | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG03927 | hp2 | a0003 | c0004 | t0001 | g0052 | SAS | BEB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0118 | SAS | STU | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG04228 | hp2 | a0006 | c0008 | t0001 | g0012 | SAS | STU | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18945 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18950 | hp1 | a0003 | c0004 | t0001 | g0056 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18956 | hp2 | a0003 | c0004 | t0001 | g0057 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18959 | hp1 | a0001 | c0005 | t0002 | g0103 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18959 | hp2 | a0004 | c0006 | t0001 | g0042 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18966 | hp2 | a0003 | c0010 | t0001 | g0050 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18974 | hp1 | a0002 | c0017 | t0002 | g0112 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18981 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18984 | hp1 | a0001 | c0005 | t0002 | g0111 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18988 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18992 | hp1 | a0001 | c0005 | t0002 | g0021 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18992 | hp2 | a0003 | c0010 | t0001 | g0092 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18993 | hp2 | a0001 | c0005 | t0014 | g0101 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA18995 | hp2 | a0003 | c0010 | t0001 | g0093 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19001 | hp1 | a0001 | c0005 | t0002 | g0102 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19005 | hp2 | a0001 | c0005 | t0011 | g0073 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19064 | hp1 | a0001 | c0005 | t0002 | g0109 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19068 | hp2 | a0004 | c0006 | t0001 | g0011 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19070 | hp1 | a0001 | c0005 | t0015 | g0099 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19070 | hp2 | a0003 | c0004 | t0001 | g0040 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19077 | hp1 | a0002 | c0026 | t0003 | g0113 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19078 | hp2 | a0004 | c0006 | t0001 | g0044 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19079 | hp2 | a0018 | c0028 | t0001 | g0037 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0046 | EAS | JPT | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19240 | hp1 | a0011 | c0013 | t0008 | g0025 | AFR | YRI | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA19240 | hp2 | a0019 | c0027 | t0017 | g0094 | AFR | YRI | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA20129 | hp1 | a0008 | c0016 | t0002 | g0128 | AFR | ASW | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ASW | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA20752 | hp1 | a0012 | c0014 | t0007 | g0009 | EUR | TSI | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA20752 | hp2 | a0012 | c0014 | t0007 | g0009 | EUR | TSI | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0125 | AFR | ACB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02109 | hp2 | a0005 | c0007 | t0004 | g0028 | AFR | ACB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02486 | hp1 | a0007 | c0009 | t0003 | g0127 | AFR | ACB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| HG02486 | hp2 | a0005 | c0007 | t0009 | g0024 | AFR | ACB | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA21309 | hp1 | a0010 | c0018 | t0001 | g0017 | AFR | LWK | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | LWK | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0130 | REF | REF | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0065 | REF | REF | FAM86B1_chr8_12177106_12199082 | FAM86B1 | chr8 | 12177106 | 12199082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12183631 | A | G | 1 | a0007 | 3 | HG02486.hp1 HG02572.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.866T>C | p.Met289Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 878/2403 | 866/891 | 289/296 | chr8 | 12183631 | |||
| chr8:12183683 | C | T | 1 | a0013 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.814G>A | p.Ala272Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 826/2403 | 814/891 | 272/296 | chr8 | 12183683 | |||
| chr8:12183700 | T | G | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.797A>C | p.Asp266Ala | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 809/2403 | 797/891 | 266/296 | chr8 | 12183700 | |||
| chr8:12183703 | C | T | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.794G>A | p.Arg265Gln | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 806/2403 | 794/891 | 265/296 | chr8 | 12183703 | |||
| chr8:12185412 | T | G | 7 | a0005 a0008 a0011 others(4): Show |
15 | HG01884.hp1 HG01975.hp2 HG02109.hp2 others(12): Show |
missense_variant | MODERATE | c.754A>C | p.Asn252His | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/7 | 766/2403 | 754/891 | 252/296 | chr8 | 12185412 | |||
| chr8:12185415 | G | T | 1 | a0012 | 2 | NA20752.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.751C>A | p.Arg251Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/7 | 763/2403 | 751/891 | 251/296 | chr8 | 12185415 | |||
| chr8:12185430 | C | T | 2 | a0014 a0017 |
2 | HG01884.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.736G>A | p.Val246Met | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/7 | 748/2403 | 736/891 | 246/296 | chr8 | 12185430 | |||
| chr8:12185523 | C | A | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant&splice_region_variant | MODERATE | c.643G>T | p.Val215Leu | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/7 | 655/2403 | 643/891 | 215/296 | chr8 | 12185523 | |||
| chr8:12185523 | C | T | 2 | a0006 a0018 |
5 | HG00642.hp1 HG01175.hp2 HG01516.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.643G>A | p.Val215Met | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/7 | 655/2403 | 643/891 | 215/296 | chr8 | 12185523 | |||
| chr8:12186364 | C | G | 4 | a0005 a0011 a0014 others(1): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
missense_variant | MODERATE | c.628G>C | p.Val210Leu | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 640/2403 | 628/891 | 210/296 | chr8 | 12186364 | |||
| chr8:12186374 | C | G | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.618G>C | p.Gln206His | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 630/2403 | 618/891 | 206/296 | chr8 | 12186374 | |||
| chr8:12186399 | A | G | 5 | a0005 a0009 a0011 others(2): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
missense_variant | MODERATE | c.593T>C | p.Met198Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 605/2403 | 593/891 | 198/296 | chr8 | 12186399 | |||
| chr8:12186421 | G | A | 4 | a0005 a0011 a0014 others(1): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
stop_gained | HIGH | c.571C>T | p.Gln191* | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 583/2403 | 571/891 | 191/296 | chr8 | 12186421 | |||
| chr8:12186441 | C | G | 4 | a0005 a0011 a0014 others(1): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
missense_variant | MODERATE | c.551G>C | p.Ser184Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 563/2403 | 551/891 | 184/296 | chr8 | 12186441 | |||
| chr8:12186501 | C | T | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.491G>A | p.Arg164Gln | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 503/2403 | 491/891 | 164/296 | chr8 | 12186501 | |||
| chr8:12186517 | C | T | 1 | a0012 | 2 | NA20752.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.475G>A | p.Val159Ile | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 487/2403 | 475/891 | 159/296 | chr8 | 12186517 | |||
| chr8:12186708 | G | C | 5 | a0003 a0004 a0006 others(2): Show |
32 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(29): Show |
missense_variant | MODERATE | c.366C>G | p.Phe122Leu | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 378/2403 | 366/891 | 122/296 | chr8 | 12186708 | |||
| chr8:12186715 | G | A | 1 | a0010 | 2 | HG01884.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.359C>T | p.Ala120Val | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 371/2403 | 359/891 | 120/296 | chr8 | 12186715 | |||
| chr8:12186739 | G | A | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.335C>T | p.Ala112Val | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 347/2403 | 335/891 | 112/296 | chr8 | 12186739 | |||
| chr8:12186755 | C | T | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.319G>A | p.Ala107Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 331/2403 | 319/891 | 107/296 | chr8 | 12186755 | |||
| chr8:12186769 | A | C | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.305T>G | p.Leu102Arg | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 317/2403 | 305/891 | 102/296 | chr8 | 12186769 | |||
| chr8:12186808 | G | C | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.266C>G | p.Ser89Cys | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 278/2403 | 266/891 | 89/296 | chr8 | 12186808 | |||
| chr8:12186829 | G | C | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
stop_gained | HIGH | c.245C>G | p.Ser82* | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 257/2403 | 245/891 | 82/296 | chr8 | 12186829 | |||
| chr8:12186833 | A | G | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant&splice_region_variant | MODERATE | c.241T>C | p.Ser81Pro | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 253/2403 | 241/891 | 81/296 | chr8 | 12186833 | |||
| chr8:12189832 | G | T | 2 | a0005 a0011 |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
stop_gained | HIGH | c.216C>A | p.Cys72* | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 228/2403 | 216/891 | 72/296 | chr8 | 12189832 | |||
| chr8:12189833 | C | A | 4 | a0003 a0004 a0015 others(1): Show |
28 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(25): Show |
missense_variant | MODERATE | c.215G>T | p.Cys72Phe | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 227/2403 | 215/891 | 72/296 | chr8 | 12189833 | |||
| chr8:12189836 | C | G | 1 | a0017 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.212G>C | p.Trp71Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 224/2403 | 212/891 | 71/296 | chr8 | 12189836 | |||
| chr8:12189837 | A | G | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.211T>C | p.Trp71Arg | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 223/2403 | 211/891 | 71/296 | chr8 | 12189837 | |||
| chr8:12189860 | T | G | 1 | a0009 | 2 | HG01070.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.188A>C | p.His63Pro | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 200/2403 | 188/891 | 63/296 | chr8 | 12189860 | |||
| chr8:12189881 | C | T | 2 | a0005 a0011 |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.167G>A | p.Arg56Lys | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 179/2403 | 167/891 | 56/296 | chr8 | 12189881 | |||
| chr8:12191811 | C | A | 9 | a0002 a0003 a0006 others(6): Show |
84 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(81): Show |
missense_variant | MODERATE | c.127G>T | p.Asp43Tyr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/7 | 139/2403 | 127/891 | 43/296 | chr8 | 12191811 | |||
| chr8:12193979 | C | T | 1 | a0005 | 6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
stop_gained | HIGH | c.92G>A | p.Trp31* | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 104/2403 | 92/891 | 31/296 | chr8 | 12193979 | |||
| chr8:12194003 | A | G | 3 | a0005 a0009 a0011 |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.68T>C | p.Val23Ala | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 80/2403 | 68/891 | 23/296 | chr8 | 12194003 | |||
| chr8:12194006 | G | A | 3 | a0005 a0009 a0011 |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.65C>T | p.Ala22Val | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 77/2403 | 65/891 | 22/296 | chr8 | 12194006 | |||
| chr8:12194016 | G | C | 1 | a0017 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.55C>G | p.Arg19Gly | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 67/2403 | 55/891 | 19/296 | chr8 | 12194016 | |||
| chr8:12194019 | G | T | 3 | a0005 a0009 a0011 |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.52C>A | p.Arg18Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 64/2403 | 52/891 | 18/296 | chr8 | 12194019 | |||
| chr8:12194028 | C | T | 2 | a0005 a0009 |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
missense_variant | MODERATE | c.43G>A | p.Gly15Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 55/2403 | 43/891 | 15/296 | chr8 | 12194028 | |||
| chr8:12194029 | C | G | 1 | a0016 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.42G>C | p.Gln14His | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 54/2403 | 42/891 | 14/296 | chr8 | 12194029 | |||
| chr8:12194043 | C | T | 3 | a0005 a0009 a0011 |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.28G>A | p.Glu10Lys | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 40/2403 | 28/891 | 10/296 | chr8 | 12194043 | |||
| chr8:12194067 | C | T | 3 | a0005 a0009 a0011 |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.4G>A | p.Ala2Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 16/2403 | 4/891 | 2/296 | chr8 | 12194067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12183648 | A | G | 6 | a0005c0007 a0005c0012 a0009c0011 others(3): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
synonymous_variant | LOW | c.849T>C | p.Tyr283Tyr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 861/2403 | 849/891 | 283/296 | chr8 | 12183648 | |||
| chr8:12183681 | C | T | 15 | a0001c0015 a0001c0024 a0002c0002 others(12): Show |
92 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.816G>A | p.Ala272Ala | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 828/2403 | 816/891 | 272/296 | chr8 | 12183681 | |||
| chr8:12183699 | A | G | 1 | a0009c0011 | 2 | HG01070.hp2 HG01257.hp1 |
synonymous_variant | LOW | c.798T>C | p.Asp266Asp | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 810/2403 | 798/891 | 266/296 | chr8 | 12183699 | |||
| chr8:12183702 | C | T | 2 | a0006c0008 a0018c0028 |
5 | HG00642.hp1 HG01175.hp2 HG01516.hp2 others(2): Show |
synonymous_variant | LOW | c.795G>A | p.Arg265Arg | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 807/2403 | 795/891 | 265/296 | chr8 | 12183702 | |||
| chr8:12185401 | C | T | 7 | a0001c0005 a0001c0023 a0002c0002 others(4): Show |
53 | HG00558.hp1 HG01070.hp1 HG01099.hp1 others(50): Show |
synonymous_variant | LOW | c.765G>A | p.Thr255Thr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/7 | 777/2403 | 765/891 | 255/296 | chr8 | 12185401 | |||
| chr8:12186371 | T | C | 1 | a0001c0021 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.621A>G | p.Pro207Pro | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 633/2403 | 621/891 | 207/296 | chr8 | 12186371 | |||
| chr8:12186401 | T | A | 1 | a0009c0011 | 2 | HG01070.hp2 HG01257.hp1 |
synonymous_variant | LOW | c.591A>T | p.Ala197Ala | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 603/2403 | 591/891 | 197/296 | chr8 | 12186401 | |||
| chr8:12186401 | T | C | 5 | a0005c0007 a0005c0012 a0011c0013 others(2): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.591A>G | p.Ala197Ala | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 603/2403 | 591/891 | 197/296 | chr8 | 12186401 | |||
| chr8:12186533 | G | A | 5 | a0005c0007 a0005c0012 a0011c0013 others(2): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.459C>T | p.Ser153Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 471/2403 | 459/891 | 153/296 | chr8 | 12186533 | |||
| chr8:12186578 | G | T | 1 | a0014c0022 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.414C>A | p.Gly138Gly | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/7 | 426/2403 | 414/891 | 138/296 | chr8 | 12186578 | |||
| chr8:12186756 | A | G | 6 | a0005c0007 a0005c0012 a0009c0011 others(3): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
synonymous_variant | LOW | c.318T>C | p.Asp106Asp | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 330/2403 | 318/891 | 106/296 | chr8 | 12186756 | |||
| chr8:12186783 | G | A | 2 | a0005c0007 a0005c0012 |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.291C>T | p.His97His | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 303/2403 | 291/891 | 97/296 | chr8 | 12186783 | |||
| chr8:12186819 | T | C | 22 | a0001c0023 a0001c0024 a0002c0002 others(19): Show |
104 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
synonymous_variant | LOW | c.255A>G | p.Ser85Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 267/2403 | 255/891 | 85/296 | chr8 | 12186819 | |||
| chr8:12186828 | T | C | 1 | a0009c0011 | 2 | HG01070.hp2 HG01257.hp1 |
synonymous_variant | LOW | c.246A>G | p.Ser82Ser | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/7 | 258/2403 | 246/891 | 82/296 | chr8 | 12186828 | |||
| chr8:12189841 | A | G | 2 | a0005c0007 a0005c0012 |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.207T>C | p.Tyr69Tyr | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/7 | 219/2403 | 207/891 | 69/296 | chr8 | 12189841 | |||
| chr8:12191796 | G | T | 4 | a0005c0007 a0005c0012 a0009c0011 others(1): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.142C>A | p.Arg48Arg | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/7 | 154/2403 | 142/891 | 48/296 | chr8 | 12191796 | |||
| chr8:12191833 | C | T | 4 | a0005c0007 a0005c0012 a0009c0011 others(1): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.105G>A | p.Glu35Glu | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/7 | 117/2403 | 105/891 | 35/296 | chr8 | 12191833 | |||
| chr8:12193990 | G | A | 3 | a0005c0007 a0005c0012 a0009c0011 |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
synonymous_variant | LOW | c.81C>T | p.Arg27Arg | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 93/2403 | 81/891 | 27/296 | chr8 | 12193990 | |||
| chr8:12194008 | C | T | 4 | a0005c0007 a0005c0012 a0009c0011 others(1): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.63G>A | p.Leu21Leu | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 75/2403 | 63/891 | 21/296 | chr8 | 12194008 | |||
| chr8:12194010 | G | A | 2 | a0005c0007 a0005c0012 |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.61C>T | p.Leu21Leu | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 73/2403 | 61/891 | 21/296 | chr8 | 12194010 | |||
| chr8:12194023 | A | G | 3 | a0005c0007 a0005c0012 a0009c0011 |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
synonymous_variant | LOW | c.48T>C | p.Phe16Phe | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 60/2403 | 48/891 | 16/296 | chr8 | 12194023 | |||
| chr8:12194047 | C | A | 4 | a0005c0007 a0005c0012 a0009c0011 others(1): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.24G>T | p.Gly8Gly | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 36/2403 | 24/891 | 8/296 | chr8 | 12194047 | |||
| chr8:12194050 | C | G | 1 | a0012c0014 | 2 | NA20752.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.21G>C | p.Ala7Ala | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 33/2403 | 21/891 | 7/296 | chr8 | 12194050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12182120 | C | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1486G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1486 | chr8 | 12182120 | ||||||
| chr8:12182132 | T | C | 15 | a0001c0023t0001 a0002c0002t0001 a0002c0002t0016 others(12): Show |
90 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1474A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1474 | chr8 | 12182132 | ||||||
| chr8:12182137 | A | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1469T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1469 | chr8 | 12182137 | ||||||
| chr8:12182211 | A | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1395T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1395 | chr8 | 12182211 | ||||||
| chr8:12182269 | G | A | 14 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(11): Show |
26 | HG01070.hp2 HG01081.hp1 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1337C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1337 | chr8 | 12182269 | ||||||
| chr8:12182271 | C | A | 3 | a0009c0011t0005 a0011c0013t0008 a0011c0013t0010 |
4 | HG01070.hp2 HG01257.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1335G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1335 | chr8 | 12182271 | ||||||
| chr8:12182292 | G | T | 1 | a0001c0015t0006 | 2 | HG00323.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1314C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1314 | chr8 | 12182292 | ||||||
| chr8:12182307 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1299A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1299 | chr8 | 12182307 | ||||||
| chr8:12182312 | G | T | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0005t0003 others(3): Show |
16 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1294C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1294 | chr8 | 12182312 | ||||||
| chr8:12182313 | C | A | 3 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1293G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1293 | chr8 | 12182313 | ||||||
| chr8:12182329 | G | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1277C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1277 | chr8 | 12182329 | ||||||
| chr8:12182350 | G | A | 1 | a0012c0014t0007 | 2 | NA20752.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1256C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1256 | chr8 | 12182350 | ||||||
| chr8:12182358 | G | A | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1248C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1248 | chr8 | 12182358 | ||||||
| chr8:12182368 | C | T | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1238G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1238 | chr8 | 12182368 | ||||||
| chr8:12182393 | A | G | 31 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(28): Show |
120 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1213T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1213 | chr8 | 12182393 | ||||||
| chr8:12182395 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1211A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1211 | chr8 | 12182395 | ||||||
| chr8:12182396 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1210C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1210 | chr8 | 12182396 | ||||||
| chr8:12182397 | G | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1209C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1209 | chr8 | 12182397 | ||||||
| chr8:12182406 | TGGGTTGT others(25): Show |
T | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1168_*1199delCCCT others(28): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1168 | chr8 | 12182406 | ||||||
| chr8:12182410 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1196A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1196 | chr8 | 12182410 | ||||||
| chr8:12182436 | G | GGGAGTTA others(211): Show |
1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1169_*1170insTCTT others(214): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1169 | chr8 | 12182436 | ||||||
| chr8:12182442 | T | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1164A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1164 | chr8 | 12182442 | ||||||
| chr8:12182446 | G | GT | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1159_*1160insA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1159 | chr8 | 12182446 | ||||||
| chr8:12182447 | A | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1159T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1159 | chr8 | 12182447 | ||||||
| chr8:12182454 | T | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1152 | chr8 | 12182454 | ||||||
| chr8:12182458 | GT | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1147delA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1147 | chr8 | 12182458 | ||||||
| chr8:12182460 | C | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1146G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1146 | chr8 | 12182460 | ||||||
| chr8:12182464 | G | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1142C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1142 | chr8 | 12182464 | ||||||
| chr8:12182467 | A | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1139T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1139 | chr8 | 12182467 | ||||||
| chr8:12182470 | GA | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1135delT | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1135 | chr8 | 12182470 | ||||||
| chr8:12182473 | T | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1133A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1133 | chr8 | 12182473 | ||||||
| chr8:12182474 | T | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1132 | chr8 | 12182474 | ||||||
| chr8:12182478 | G | GTCAGCAG others(717): Show |
1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1127_*1128insGTGG others(720): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1127 | chr8 | 12182478 | ||||||
| chr8:12182519 | T | G | 9 | a0001c0005t0014 a0005c0007t0004 a0005c0007t0009 others(6): Show |
13 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1087A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1087 | chr8 | 12182519 | ||||||
| chr8:12182523 | A | G | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1083T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1083 | chr8 | 12182523 | ||||||
| chr8:12182527 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1079C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1079 | chr8 | 12182527 | ||||||
| chr8:12182547 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1059 | chr8 | 12182547 | ||||||
| chr8:12182560 | T | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1046A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1046 | chr8 | 12182560 | ||||||
| chr8:12182582 | T | G | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1024A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1024 | chr8 | 12182582 | ||||||
| chr8:12182606 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1000A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 1000 | chr8 | 12182606 | ||||||
| chr8:12182617 | A | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*989T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 989 | chr8 | 12182617 | ||||||
| chr8:12182628 | G | A | 31 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(28): Show |
120 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*978C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 978 | chr8 | 12182628 | ||||||
| chr8:12182632 | G | A | 1 | a0001c0005t0015 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*974C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 974 | chr8 | 12182632 | ||||||
| chr8:12182636 | T | C | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*970A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 970 | chr8 | 12182636 | ||||||
| chr8:12182639 | A | C | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*967T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 967 | chr8 | 12182639 | ||||||
| chr8:12182649 | A | G | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*957T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 957 | chr8 | 12182649 | ||||||
| chr8:12182650 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*956T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 956 | chr8 | 12182650 | ||||||
| chr8:12182656 | T | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*950A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 950 | chr8 | 12182656 | ||||||
| chr8:12182751 | C | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*855G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 855 | chr8 | 12182751 | ||||||
| chr8:12182769 | G | GCTT | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*834_*836dupAAG | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 836 | chr8 | 12182769 | ||||||
| chr8:12182792 | G | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*814C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 814 | chr8 | 12182792 | ||||||
| chr8:12182798 | C | T | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*808G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 808 | chr8 | 12182798 | ||||||
| chr8:12182799 | G | A | 1 | a0019c0027t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*807C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 807 | chr8 | 12182799 | ||||||
| chr8:12182806 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*800C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 800 | chr8 | 12182806 | ||||||
| chr8:12182816 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*790C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 790 | chr8 | 12182816 | ||||||
| chr8:12182835 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*771C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 771 | chr8 | 12182835 | ||||||
| chr8:12182845 | T | C | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*761A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 761 | chr8 | 12182845 | ||||||
| chr8:12182859 | AC | A | 3 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*746delG | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 746 | chr8 | 12182859 | ||||||
| chr8:12182897 | A | G | 2 | a0014c0022t0020 a0017c0030t0019 |
2 | HG01884.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*709T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 709 | chr8 | 12182897 | ||||||
| chr8:12182908 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 698 | chr8 | 12182908 | ||||||
| chr8:12182916 | G | GTCT | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*687_*689dupAGA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 689 | chr8 | 12182916 | ||||||
| chr8:12182923 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 683 | chr8 | 12182923 | ||||||
| chr8:12182924 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 682 | chr8 | 12182924 | ||||||
| chr8:12182931 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*675A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 675 | chr8 | 12182931 | ||||||
| chr8:12182933 | C | A | 1 | a0001c0024t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*673G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 673 | chr8 | 12182933 | ||||||
| chr8:12182949 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*657C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 657 | chr8 | 12182949 | ||||||
| chr8:12182950 | C | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*656G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 656 | chr8 | 12182950 | ||||||
| chr8:12182959 | G | A | 2 | a0011c0013t0008 a0011c0013t0010 |
2 | HG03209.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*647C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 647 | chr8 | 12182959 | ||||||
| chr8:12182968 | C | T | 2 | a0011c0013t0008 a0011c0013t0010 |
2 | HG03209.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*638G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 638 | chr8 | 12182968 | ||||||
| chr8:12182971 | C | A | 3 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*635G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 635 | chr8 | 12182971 | ||||||
| chr8:12183013 | C | T | 1 | a0002c0002t0016 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 593 | chr8 | 12183013 | ||||||
| chr8:12183020 | C | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 586 | chr8 | 12183020 | ||||||
| chr8:12183032 | G | A | 14 | a0001c0023t0001 a0002c0002t0001 a0002c0002t0016 others(11): Show |
88 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*574C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 574 | chr8 | 12183032 | ||||||
| chr8:12183039 | T | C | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*567A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 567 | chr8 | 12183039 | ||||||
| chr8:12183041 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*565T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 565 | chr8 | 12183041 | ||||||
| chr8:12183048 | C | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*558G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 558 | chr8 | 12183048 | ||||||
| chr8:12183069 | G | A | 2 | a0009c0011t0005 a0012c0014t0007 |
4 | HG01070.hp2 HG01257.hp1 NA20752.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*537C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 537 | chr8 | 12183069 | ||||||
| chr8:12183069 | G | C | 1 | a0001c0001t0013 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 537 | chr8 | 12183069 | ||||||
| chr8:12183073 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*533C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 533 | chr8 | 12183073 | ||||||
| chr8:12183089 | TGGGATGT others(45): Show |
T | 2 | a0001c0024t0018 a0012c0014t0007 |
3 | HG02886.hp2 NA20752.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*465_*516delTGGACA others(46): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 465 | chr8 | 12183089 | ||||||
| chr8:12183089 | TGGGATGT others(97): Show |
T | 22 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(19): Show |
106 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*516del | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 413 | chr8 | 12183089 | ||||||
| chr8:12183121 | G | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*485C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 485 | chr8 | 12183121 | ||||||
| chr8:12183136 | T | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*470A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 470 | chr8 | 12183136 | ||||||
| chr8:12183178 | G | A | 1 | a0001c0024t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 428 | chr8 | 12183178 | ||||||
| chr8:12183182 | C | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*424G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 424 | chr8 | 12183182 | ||||||
| chr8:12183185 | G | C | 1 | a0005c0012t0004 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 421 | chr8 | 12183185 | ||||||
| chr8:12183188 | T | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*418A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 418 | chr8 | 12183188 | ||||||
| chr8:12183192 | C | T | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 414 | chr8 | 12183192 | ||||||
| chr8:12183212 | C | T | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*394G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 394 | chr8 | 12183212 | ||||||
| chr8:12183227 | G | A | 1 | a0014c0022t0020 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 379 | chr8 | 12183227 | ||||||
| chr8:12183235 | G | A | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*371C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 371 | chr8 | 12183235 | ||||||
| chr8:12183257 | G | A | 7 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*349C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 349 | chr8 | 12183257 | ||||||
| chr8:12183287 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*319C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 319 | chr8 | 12183287 | ||||||
| chr8:12183301 | T | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*305A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 305 | chr8 | 12183301 | ||||||
| chr8:12183313 | A | G | 1 | a0012c0014t0007 | 2 | NA20752.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*293T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 293 | chr8 | 12183313 | ||||||
| chr8:12183343 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*263T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 263 | chr8 | 12183343 | ||||||
| chr8:12183365 | T | C | 24 | a0001c0023t0001 a0001c0024t0018 a0002c0002t0001 others(21): Show |
103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*241A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 241 | chr8 | 12183365 | ||||||
| chr8:12183367 | G | A | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*239C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 239 | chr8 | 12183367 | ||||||
| chr8:12183389 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*217T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 217 | chr8 | 12183389 | ||||||
| chr8:12183400 | G | A | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 206 | chr8 | 12183400 | ||||||
| chr8:12183440 | C | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*166G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 166 | chr8 | 12183440 | ||||||
| chr8:12183450 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*156T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 156 | chr8 | 12183450 | ||||||
| chr8:12183472 | T | TG | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*133_*134insC | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 133 | chr8 | 12183472 | ||||||
| chr8:12183475 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*131T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 131 | chr8 | 12183475 | ||||||
| chr8:12183489 | G | A | 24 | a0001c0023t0001 a0001c0024t0018 a0002c0002t0001 others(21): Show |
103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 117 | chr8 | 12183489 | ||||||
| chr8:12183495 | T | C | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 111 | chr8 | 12183495 | ||||||
| chr8:12183511 | C | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*95G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 95 | chr8 | 12183511 | ||||||
| chr8:12183533 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*73T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 73 | chr8 | 12183533 | ||||||
| chr8:12183585 | C | T | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 21 | chr8 | 12183585 | ||||||
| chr8:12183586 | T | G | 8 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(5): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*20A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 20 | chr8 | 12183586 | ||||||
| chr8:12183595 | A | G | 1 | a0009c0011t0005 | 2 | HG01070.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 7/7 | 11 | chr8 | 12183595 | ||||||
| chr8:12194071 | A | G | 6 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(3): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-1T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 1 | chr8 | 12194071 | ||||||
| chr8:12194073 | C | T | 6 | a0005c0007t0004 a0005c0007t0009 a0005c0012t0004 others(3): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-3G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 3 | chr8 | 12194073 | ||||||
| chr8:12194080 | GA | G | 2 | a0005c0007t0009 a0011c0013t0008 |
2 | HG02486.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-11delT | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 11 | chr8 | 12194080 | ||||||
| chr8:12194081 | A | G | 6 | a0005c0007t0004 a0005c0012t0004 a0009c0011t0005 others(3): Show |
11 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-11T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/7 | 11 | chr8 | 12194081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12183792 | C | T | 1 | a0001c0005t0002g0102 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.791-86G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183792 | |||||||
| chr8:12183796 | G | T | 1 | a0001c0001t0002g0045 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.791-90C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183796 | |||||||
| chr8:12183803 | G | T | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.791-97C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183803 | |||||||
| chr8:12183804 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-98A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183804 | |||||||
| chr8:12183824 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-118C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183824 | |||||||
| chr8:12183837 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-131C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183837 | |||||||
| chr8:12183840 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.791-134C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183840 | |||||||
| chr8:12183850 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-144T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183850 | |||||||
| chr8:12183862 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-156G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183862 | |||||||
| chr8:12183863 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.791-157C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183863 | |||||||
| chr8:12183884 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-178G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183884 | |||||||
| chr8:12183886 | C | A | 3 | a0008c0016t0002g0069 a0008c0016t0002g0128 a0008c0020t0002g0068 |
3 | HG03139.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.791-180G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183886 | |||||||
| chr8:12183888 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-182C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183888 | |||||||
| chr8:12183938 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-232C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183938 | |||||||
| chr8:12183946 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-240C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183946 | |||||||
| chr8:12183979 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-273C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183979 | |||||||
| chr8:12183994 | C | T | 4 | a0011c0013t0008g0025 a0011c0013t0010g0033 a0014c0022t0020g0132 others(1): Show |
4 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.791-288G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183994 | |||||||
| chr8:12183999 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-293G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12183999 | |||||||
| chr8:12184001 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-295G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184001 | |||||||
| chr8:12184014 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-308C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184014 | |||||||
| chr8:12184034 | G | T | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.791-328C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184034 | |||||||
| chr8:12184041 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-335T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184041 | |||||||
| chr8:12184070 | C | CAAAAAA | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.791-370_791-365dup others(6): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184070 | |||||||
| chr8:12184070 | CA | C | 78 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(75): Show |
107 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.791-365delT | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184070 | |||||||
| chr8:12184085 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-379C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184085 | |||||||
| chr8:12184094 | A | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.791-388T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184094 | |||||||
| chr8:12184094 | A | G | 4 | a0009c0011t0005g0026 a0009c0011t0005g0027 a0011c0013t0008g0025 others(1): Show |
4 | HG01070.hp2 HG01257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.791-388T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184094 | |||||||
| chr8:12184095 | G | A | 6 | a0002c0003t0001g0016 a0005c0007t0004g0028 a0005c0007t0004g0031 others(3): Show |
7 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.791-389C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184095 | |||||||
| chr8:12184108 | T | G | 28 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0005 others(25): Show |
46 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.791-402A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184108 | |||||||
| chr8:12184163 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-457C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184163 | |||||||
| chr8:12184183 | T | G | 1 | a0001c0001t0002g0019 | 2 | NA18940.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.791-477A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184183 | |||||||
| chr8:12184186 | C | CT | 19 | a0001c0001t0002g0022 a0001c0001t0002g0096 a0001c0001t0002g0105 others(16): Show |
22 | HG00423.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.791-481dupA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184186 | |||||||
| chr8:12184186 | CTTTT | C | 11 | a0002c0002t0001g0005 a0002c0002t0001g0080 a0002c0002t0001g0082 others(8): Show |
13 | HG01081.hp2 HG01433.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.791-484_791-481del others(4): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184186 | |||||||
| chr8:12184186 | CTTTTT | C | 48 | a0001c0023t0001g0067 a0001c0024t0018g0035 a0002c0002t0001g0001 others(45): Show |
72 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.791-485_791-481del others(5): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184186 | |||||||
| chr8:12184186 | CTTTTTT | C | 7 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0012t0004g0030 others(4): Show |
9 | HG01884.hp2 HG02109.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.791-486_791-481del others(6): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184186 | |||||||
| chr8:12184186 | CTTTTTTT | C | 5 | a0002c0003t0001g0061 a0005c0007t0004g0032 a0005c0007t0009g0024 others(2): Show |
5 | HG02148.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.791-487_791-481del others(7): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184186 | |||||||
| chr8:12184215 | CT | C | 31 | a0002c0002t0001g0004 a0002c0002t0001g0076 a0002c0002t0001g0084 others(28): Show |
39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.791-510delA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184215 | |||||||
| chr8:12184251 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-545T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184251 | |||||||
| chr8:12184262 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-556T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184262 | |||||||
| chr8:12184270 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.791-564C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184270 | |||||||
| chr8:12184303 | A | G | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-597T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184303 | |||||||
| chr8:12184310 | G | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-604C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184310 | |||||||
| chr8:12184356 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-650A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184356 | |||||||
| chr8:12184357 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-651C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184357 | |||||||
| chr8:12184369 | A | G | 1 | a0006c0008t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.791-663T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184369 | |||||||
| chr8:12184402 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-696C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184402 | |||||||
| chr8:12184404 | GT | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.791-699delA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184404 | |||||||
| chr8:12184409 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.791-703T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184409 | |||||||
| chr8:12184412 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-706T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184412 | |||||||
| chr8:12184422 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-716T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184422 | |||||||
| chr8:12184429 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-723G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184429 | |||||||
| chr8:12184438 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-732A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184438 | |||||||
| chr8:12184452 | T | A | 16 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(13): Show |
17 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.791-746A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184452 | |||||||
| chr8:12184461 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-755A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184461 | |||||||
| chr8:12184467 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-761A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184467 | |||||||
| chr8:12184500 | C | T | 5 | a0003c0010t0001g0092 a0011c0013t0008g0025 a0011c0013t0010g0033 others(2): Show |
5 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.791-794G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184500 | |||||||
| chr8:12184501 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-795C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184501 | |||||||
| chr8:12184502 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.791-796G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184502 | |||||||
| chr8:12184507 | G | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.791-801C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184507 | |||||||
| chr8:12184510 | C | G | 2 | a0014c0022t0020g0132 a0017c0030t0019g0134 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.791-804G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184510 | |||||||
| chr8:12184522 | C | T | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.791-816G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184522 | |||||||
| chr8:12184532 | T | C | 13 | a0001c0024t0018g0035 a0005c0007t0004g0028 a0005c0007t0004g0031 others(10): Show |
13 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.791-826A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184532 | |||||||
| chr8:12184544 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+832T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184544 | |||||||
| chr8:12184556 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+820T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184556 | |||||||
| chr8:12184564 | A | G | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.790+812T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184564 | |||||||
| chr8:12184566 | G | T | 25 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0005 others(22): Show |
43 | HG00423.hp2 HG00558.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.790+810C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184566 | |||||||
| chr8:12184572 | G | A | 17 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0005 others(14): Show |
32 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.790+804C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184572 | |||||||
| chr8:12184597 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.790+779A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184597 | |||||||
| chr8:12184628 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+748T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184628 | |||||||
| chr8:12184632 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+744T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184632 | |||||||
| chr8:12184644 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+732T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184644 | |||||||
| chr8:12184666 | A | G | 4 | a0009c0011t0005g0026 a0009c0011t0005g0027 a0011c0013t0008g0025 others(1): Show |
4 | HG01070.hp2 HG01257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.790+710T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184666 | |||||||
| chr8:12184726 | G | T | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.790+650C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184726 | |||||||
| chr8:12184747 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+629C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184747 | |||||||
| chr8:12184791 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+585C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184791 | |||||||
| chr8:12184806 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+570T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184806 | |||||||
| chr8:12184837 | C | T | 1 | a0002c0003t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.790+539G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184837 | |||||||
| chr8:12184844 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+532T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184844 | |||||||
| chr8:12184882 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+494A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184882 | |||||||
| chr8:12184910 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+466C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184910 | |||||||
| chr8:12184922 | C | T | 1 | a0007c0009t0003g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.790+454G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184922 | |||||||
| chr8:12184938 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+438A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184938 | |||||||
| chr8:12184954 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+422C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184954 | |||||||
| chr8:12184957 | C | T | 6 | a0009c0011t0005g0026 a0009c0011t0005g0027 a0011c0013t0008g0025 others(3): Show |
6 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.790+419G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184957 | |||||||
| chr8:12184958 | G | A | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.790+418C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184958 | |||||||
| chr8:12184995 | T | A | 4 | a0009c0011t0005g0026 a0009c0011t0005g0027 a0014c0022t0020g0132 others(1): Show |
4 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.790+381A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184995 | |||||||
| chr8:12184996 | G | A | 2 | a0002c0002t0001g0082 a0002c0002t0001g0083 |
2 | NA18956.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.790+380C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12184996 | |||||||
| chr8:12185002 | G | A | 1 | a0003c0004t0001g0052 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.790+374C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185002 | |||||||
| chr8:12185013 | C | T | 1 | a0018c0028t0001g0037 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.790+363G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185013 | |||||||
| chr8:12185025 | G | A | 7 | a0005c0007t0004g0031 a0005c0007t0004g0032 a0005c0007t0009g0024 others(4): Show |
7 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.790+351C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185025 | |||||||
| chr8:12185034 | T | G | 25 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(22): Show |
26 | HG01070.hp2 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.790+342A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185034 | |||||||
| chr8:12185040 | G | T | 1 | a0003c0004t0001g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.790+336C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185040 | |||||||
| chr8:12185041 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+335G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185041 | |||||||
| chr8:12185057 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+319G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185057 | |||||||
| chr8:12185058 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+318G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185058 | |||||||
| chr8:12185061 | G | A | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.790+315C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185061 | |||||||
| chr8:12185067 | C | T | 4 | a0002c0002t0001g0014 a0002c0002t0001g0080 a0002c0002t0001g0131 others(1): Show |
5 | HG00558.hp1 NA18940.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+309G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185067 | |||||||
| chr8:12185068 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+308C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185068 | |||||||
| chr8:12185072 | C | T | 22 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(19): Show |
24 | HG01081.hp1 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.790+304G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185072 | |||||||
| chr8:12185074 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+302C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185074 | |||||||
| chr8:12185081 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+295G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185081 | |||||||
| chr8:12185082 | C | G | 2 | a0002c0002t0001g0082 a0002c0002t0001g0083 |
2 | NA18956.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.790+294G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185082 | |||||||
| chr8:12185097 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+279C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185097 | |||||||
| chr8:12185103 | G | A | 68 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(65): Show |
95 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.790+273C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185103 | |||||||
| chr8:12185105 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.790+271C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185105 | |||||||
| chr8:12185106 | G | A | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.790+270C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185106 | |||||||
| chr8:12185109 | C | T | 5 | a0011c0013t0008g0025 a0011c0013t0010g0033 a0014c0022t0020g0132 others(2): Show |
5 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+267G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185109 | |||||||
| chr8:12185110 | A | G | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.790+266T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185110 | |||||||
| chr8:12185112 | G | C | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.790+264C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185112 | |||||||
| chr8:12185120 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+256C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185120 | |||||||
| chr8:12185127 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.790+249A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185127 | |||||||
| chr8:12185141 | T | C | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.790+235A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185141 | |||||||
| chr8:12185164 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+212G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185164 | |||||||
| chr8:12185171 | C | G | 1 | a0019c0027t0017g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.790+205G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185171 | |||||||
| chr8:12185178 | C | A | 24 | a0003c0004t0001g0002 a0003c0004t0001g0010 a0003c0004t0001g0039 others(21): Show |
30 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.790+198G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185178 | |||||||
| chr8:12185185 | G | A | 16 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(13): Show |
17 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.790+191C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185185 | |||||||
| chr8:12185199 | T | G | 60 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(57): Show |
87 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.790+177A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185199 | |||||||
| chr8:12185211 | C | T | 1 | a0001c0005t0002g0104 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.790+165G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185211 | |||||||
| chr8:12185233 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.790+143G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185233 | |||||||
| chr8:12185234 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+142G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185234 | |||||||
| chr8:12185235 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.790+141C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185235 | |||||||
| chr8:12185236 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.790+140C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185236 | |||||||
| chr8:12185257 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+119T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185257 | |||||||
| chr8:12185259 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+117T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185259 | |||||||
| chr8:12185274 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+102T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185274 | |||||||
| chr8:12185279 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+97G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185279 | |||||||
| chr8:12185284 | C | T | 2 | a0014c0022t0020g0132 a0017c0030t0019g0134 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.790+92G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185284 | |||||||
| chr8:12185293 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.790+83T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185293 | |||||||
| chr8:12185295 | C | T | 3 | a0001c0024t0018g0035 a0009c0011t0005g0026 a0009c0011t0005g0027 |
3 | HG01070.hp2 HG01257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.790+81G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185295 | |||||||
| chr8:12185296 | G | A | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
10 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.790+80C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185296 | |||||||
| chr8:12185312 | T | C | 69 | a0001c0001t0002g0114 a0001c0023t0001g0067 a0002c0002t0001g0001 others(66): Show |
95 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.790+64A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185312 | |||||||
| chr8:12185313 | C | T | 69 | a0001c0001t0002g0114 a0001c0023t0001g0067 a0002c0002t0001g0001 others(66): Show |
95 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.790+63G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185313 | |||||||
| chr8:12185342 | C | G | 17 | a0001c0024t0018g0035 a0002c0003t0001g0090 a0005c0007t0004g0028 others(14): Show |
18 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.790+34G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185342 | |||||||
| chr8:12185349 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.790+27A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185349 | |||||||
| chr8:12185355 | CG | C | 14 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.790+20delC | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185355 | |||||||
| chr8:12185371 | T | C | 93 | a0001c0001t0002g0022 a0001c0001t0002g0045 a0001c0001t0002g0074 others(90): Show |
122 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(119): Show |
splice_region_variant&intron_variant | LOW | c.790+5A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 6/6 | chr8 | 12185371 | |||||||
| chr8:12185530 | G | A | 26 | a0003c0004t0001g0002 a0003c0004t0001g0010 a0003c0004t0001g0039 others(23): Show |
32 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.641-5C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185530 | |||||||
| chr8:12185538 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-13A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185538 | |||||||
| chr8:12185544 | G | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.641-19C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185544 | |||||||
| chr8:12185551 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-26T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185551 | |||||||
| chr8:12185569 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-44A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185569 | |||||||
| chr8:12185574 | G | T | 62 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(59): Show |
89 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.641-49C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185574 | |||||||
| chr8:12185581 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-56G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185581 | |||||||
| chr8:12185599 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-74G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185599 | |||||||
| chr8:12185617 | G | A | 3 | a0009c0011t0005g0026 a0009c0011t0005g0027 a0010c0018t0001g0017 |
4 | HG01070.hp2 HG01257.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-92C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185617 | |||||||
| chr8:12185633 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-108A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185633 | |||||||
| chr8:12185642 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-117A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185642 | |||||||
| chr8:12185664 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-139A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185664 | |||||||
| chr8:12185674 | A | T | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.641-149T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185674 | |||||||
| chr8:12185678 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-153A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185678 | |||||||
| chr8:12185702 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-177T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185702 | |||||||
| chr8:12185703 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-178A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185703 | |||||||
| chr8:12185715 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-190C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185715 | |||||||
| chr8:12185759 | G | GT | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-235dupA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185759 | |||||||
| chr8:12185770 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-245T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185770 | |||||||
| chr8:12185774 | G | A | 34 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(31): Show |
54 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.641-249C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185774 | |||||||
| chr8:12185780 | G | T | 1 | a0003c0004t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.641-255C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185780 | |||||||
| chr8:12185785 | C | T | 2 | a0014c0022t0020g0132 a0017c0030t0019g0134 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.641-260G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185785 | |||||||
| chr8:12185786 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-261C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185786 | |||||||
| chr8:12185788 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-263G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185788 | |||||||
| chr8:12185791 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-266C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185791 | |||||||
| chr8:12185805 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-280G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185805 | |||||||
| chr8:12185823 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-298G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185823 | |||||||
| chr8:12185835 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-310G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185835 | |||||||
| chr8:12185850 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-325C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185850 | |||||||
| chr8:12185893 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.641-368G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185893 | |||||||
| chr8:12185929 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.641-404C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185929 | |||||||
| chr8:12185939 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+413A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185939 | |||||||
| chr8:12185950 | T | A | 5 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+402A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185950 | |||||||
| chr8:12185950 | T | C | 69 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(66): Show |
96 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.640+402A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185950 | |||||||
| chr8:12185954 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+398C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185954 | |||||||
| chr8:12185973 | T | C | 1 | a0010c0018t0001g0017 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.640+379A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185973 | |||||||
| chr8:12185983 | C | G | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+369G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185983 | |||||||
| chr8:12185984 | A | G | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+368T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12185984 | |||||||
| chr8:12186002 | C | T | 72 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(69): Show |
99 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.640+350G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186002 | |||||||
| chr8:12186003 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+349C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186003 | |||||||
| chr8:12186014 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+338G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186014 | |||||||
| chr8:12186020 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+332C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186020 | |||||||
| chr8:12186042 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+310T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186042 | |||||||
| chr8:12186047 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+305C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186047 | |||||||
| chr8:12186049 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+303T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186049 | |||||||
| chr8:12186074 | C | T | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+278G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186074 | |||||||
| chr8:12186090 | C | A | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.640+262G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186090 | |||||||
| chr8:12186090 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+262G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186090 | |||||||
| chr8:12186108 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+244G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186108 | |||||||
| chr8:12186123 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+229T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186123 | |||||||
| chr8:12186133 | C | T | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+219G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186133 | |||||||
| chr8:12186134 | T | G | 93 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0003g0023 others(90): Show |
122 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.640+218A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186134 | |||||||
| chr8:12186135 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+217C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186135 | |||||||
| chr8:12186136 | T | G | 93 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0003g0023 others(90): Show |
122 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.640+216A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186136 | |||||||
| chr8:12186157 | C | G | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+195G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186157 | |||||||
| chr8:12186176 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+176A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186176 | |||||||
| chr8:12186182 | T | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+170A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186182 | |||||||
| chr8:12186208 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+144G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186208 | |||||||
| chr8:12186250 | A | G | 76 | a0001c0023t0001g0067 a0001c0024t0018g0035 a0002c0002t0001g0001 others(73): Show |
104 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.640+102T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186250 | |||||||
| chr8:12186259 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+93G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186259 | |||||||
| chr8:12186265 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+87A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186265 | |||||||
| chr8:12186310 | C | T | 1 | a0002c0003t0001g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.640+42G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186310 | |||||||
| chr8:12186319 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.640+33G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186319 | |||||||
| chr8:12186349 | T | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.640+3A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 5/6 | chr8 | 12186349 | |||||||
| chr8:12186627 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.375-10C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/6 | chr8 | 12186627 | |||||||
| chr8:12186643 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.375-26A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/6 | chr8 | 12186643 | |||||||
| chr8:12186666 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.374+34A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/6 | chr8 | 12186666 | |||||||
| chr8:12186669 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.374+31G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/6 | chr8 | 12186669 | |||||||
| chr8:12186672 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.374+28C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/6 | chr8 | 12186672 | |||||||
| chr8:12186692 | A | G | 74 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0004 others(71): Show |
101 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(98): Show |
splice_region_variant&intron_variant | LOW | c.374+8T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 4/6 | chr8 | 12186692 | |||||||
| chr8:12186836 | G | T | 1 | a0004c0006t0001g0044 | 1 | NA19078.hp2 | splice_region_variant&intron_variant | LOW | c.241-3C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186836 | |||||||
| chr8:12186839 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
splice_region_variant&intron_variant | LOW | c.241-6G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186839 | |||||||
| chr8:12186840 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.241-7G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186840 | |||||||
| chr8:12186926 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-93G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186926 | |||||||
| chr8:12186942 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-109C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186942 | |||||||
| chr8:12186960 | G | A | 2 | a0001c0001t0002g0074 a0001c0005t0011g0073 |
2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.241-127C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186960 | |||||||
| chr8:12186968 | C | T | 1 | a0004c0006t0001g0042 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.241-135G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186968 | |||||||
| chr8:12186985 | G | GC | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-153_241-152ins others(1): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186985 | |||||||
| chr8:12186988 | G | T | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-155C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12186988 | |||||||
| chr8:12187000 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-167T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187000 | |||||||
| chr8:12187011 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-178G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187011 | |||||||
| chr8:12187013 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0120 a0001c0005t0003g0119 others(1): Show |
5 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-180C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187013 | |||||||
| chr8:12187053 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-220A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187053 | |||||||
| chr8:12187062 | T | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-229A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187062 | |||||||
| chr8:12187074 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-241G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187074 | |||||||
| chr8:12187074 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-241G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187074 | |||||||
| chr8:12187078 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-245T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187078 | |||||||
| chr8:12187099 | T | TA | 1 | a0010c0018t0001g0017 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.241-267_241-266ins others(1): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187099 | |||||||
| chr8:12187127 | T | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-294A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187127 | |||||||
| chr8:12187134 | A | G | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-301T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187134 | |||||||
| chr8:12187137 | T | G | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG02523.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.241-304A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187137 | |||||||
| chr8:12187139 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-306C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187139 | |||||||
| chr8:12187154 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-321A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187154 | |||||||
| chr8:12187205 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-372G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187205 | |||||||
| chr8:12187206 | AT | A | 61 | a0001c0001t0002g0020 a0001c0001t0002g0100 a0001c0005t0002g0070 others(58): Show |
89 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.241-374delA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187206 | |||||||
| chr8:12187206 | ATT | A | 38 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(35): Show |
48 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.241-375_241-374del others(2): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187206 | |||||||
| chr8:12187206 | ATTT | A | 16 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(13): Show |
18 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-376_241-374del others(3): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187206 | |||||||
| chr8:12187206 | ATTTTTT | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-379_241-374del others(6): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187206 | |||||||
| chr8:12187233 | A | C | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.241-400T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187233 | |||||||
| chr8:12187235 | C | A | 1 | a0002c0003t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.241-402G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187235 | |||||||
| chr8:12187239 | G | A | 1 | a0005c0007t0009g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.241-406C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187239 | |||||||
| chr8:12187245 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-412C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187245 | |||||||
| chr8:12187252 | G | A | 1 | a0002c0002t0001g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.241-419C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187252 | |||||||
| chr8:12187263 | G | T | 1 | a0002c0002t0001g0015 | 2 | NA18969.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.241-430C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187263 | |||||||
| chr8:12187266 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-433A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187266 | |||||||
| chr8:12187275 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-442T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187275 | |||||||
| chr8:12187311 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-478G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187311 | |||||||
| chr8:12187315 | C | T | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-482G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187315 | |||||||
| chr8:12187319 | G | A | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-486C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187319 | |||||||
| chr8:12187338 | G | A | 2 | a0014c0022t0020g0132 a0017c0030t0019g0134 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.241-505C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187338 | |||||||
| chr8:12187353 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-520A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187353 | |||||||
| chr8:12187354 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-521T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187354 | |||||||
| chr8:12187383 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-550G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187383 | |||||||
| chr8:12187397 | T | C | 1 | a0007c0009t0003g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.241-564A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187397 | |||||||
| chr8:12187401 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-568G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187401 | |||||||
| chr8:12187417 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-584A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187417 | |||||||
| chr8:12187437 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-604T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187437 | |||||||
| chr8:12187452 | C | T | 4 | a0001c0023t0001g0067 a0005c0007t0004g0032 a0005c0007t0009g0024 others(1): Show |
4 | HG01099.hp1 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-619G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187452 | |||||||
| chr8:12187454 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-621C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187454 | |||||||
| chr8:12187459 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-626T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187459 | |||||||
| chr8:12187485 | G | C | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-652C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187485 | |||||||
| chr8:12187490 | A | G | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-657T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187490 | |||||||
| chr8:12187504 | C | T | 1 | a0008c0016t0002g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.241-671G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187504 | |||||||
| chr8:12187521 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-688G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187521 | |||||||
| chr8:12187523 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-690A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187523 | |||||||
| chr8:12187551 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-718T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187551 | |||||||
| chr8:12187552 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-719A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187552 | |||||||
| chr8:12187554 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-721A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187554 | |||||||
| chr8:12187562 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-729C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187562 | |||||||
| chr8:12187586 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-753G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187586 | |||||||
| chr8:12187591 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-758G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187591 | |||||||
| chr8:12187594 | A | T | 1 | a0002c0003t0001g0060 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.241-761T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187594 | |||||||
| chr8:12187601 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-768G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187601 | |||||||
| chr8:12187606 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-773A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187606 | |||||||
| chr8:12187622 | T | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-789A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187622 | |||||||
| chr8:12187638 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-805T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187638 | |||||||
| chr8:12187640 | A | G | 1 | a0002c0002t0016g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.241-807T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187640 | |||||||
| chr8:12187651 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-818G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187651 | |||||||
| chr8:12187694 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-861G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187694 | |||||||
| chr8:12187739 | C | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
86 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.241-906G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187739 | |||||||
| chr8:12187741 | C | T | 3 | a0001c0001t0003g0129 a0001c0001t0013g0118 a0003c0004t0001g0048 |
3 | HG01261.hp2 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.241-908G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187741 | |||||||
| chr8:12187746 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-913C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187746 | |||||||
| chr8:12187751 | C | T | 1 | a0002c0002t0016g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.241-918G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187751 | |||||||
| chr8:12187765 | T | G | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.241-932A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187765 | |||||||
| chr8:12187769 | A | T | 1 | a0001c0001t0002g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.241-936T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187769 | |||||||
| chr8:12187773 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-940T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187773 | |||||||
| chr8:12187778 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-945T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187778 | |||||||
| chr8:12187779 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-946C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187779 | |||||||
| chr8:12187785 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-952C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187785 | |||||||
| chr8:12187841 | T | C | 1 | a0002c0003t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.241-1008A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187841 | |||||||
| chr8:12187860 | G | A | 2 | a0004c0006t0001g0043 a0004c0006t0001g0044 |
2 | HG02148.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.241-1027C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187860 | |||||||
| chr8:12187860 | G | T | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-1027C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187860 | |||||||
| chr8:12187865 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1032T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187865 | |||||||
| chr8:12187890 | CTGT | C | 26 | a0003c0004t0001g0002 a0003c0004t0001g0010 a0003c0004t0001g0039 others(23): Show |
32 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.241-1060_241-1058d others(5): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187890 | |||||||
| chr8:12187898 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1065C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187898 | |||||||
| chr8:12187958 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1125C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12187958 | |||||||
| chr8:12188062 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1229A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188062 | |||||||
| chr8:12188085 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1252G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188085 | |||||||
| chr8:12188098 | T | G | 2 | a0005c0007t0004g0032 a0005c0007t0009g0024 |
2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.241-1265A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188098 | |||||||
| chr8:12188123 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1290G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188123 | |||||||
| chr8:12188125 | T | C | 90 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(87): Show |
119 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.241-1292A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188125 | |||||||
| chr8:12188126 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1293C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188126 | |||||||
| chr8:12188130 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1297T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188130 | |||||||
| chr8:12188141 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-1308A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188141 | |||||||
| chr8:12188143 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-1310A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188143 | |||||||
| chr8:12188144 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1311C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188144 | |||||||
| chr8:12188153 | C | T | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.241-1320G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188153 | |||||||
| chr8:12188170 | C | T | 13 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(10): Show |
14 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.241-1337G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188170 | |||||||
| chr8:12188171 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1338C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188171 | |||||||
| chr8:12188229 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-1396G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188229 | |||||||
| chr8:12188236 | AT | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-1404delA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188236 | |||||||
| chr8:12188246 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0080 a0002c0003t0001g0079 |
4 | HG00558.hp1 NA19005.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1413T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188246 | |||||||
| chr8:12188270 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1437C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188270 | |||||||
| chr8:12188277 | G | A | 56 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(53): Show |
82 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.241-1444C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188277 | |||||||
| chr8:12188282 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1449T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188282 | |||||||
| chr8:12188285 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1452C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188285 | |||||||
| chr8:12188306 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-1473G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188306 | |||||||
| chr8:12188310 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.241-1477G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188310 | |||||||
| chr8:12188314 | G | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-1481C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188314 | |||||||
| chr8:12188327 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1481C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188327 | |||||||
| chr8:12188334 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1474A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188334 | |||||||
| chr8:12188336 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+1472C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188336 | |||||||
| chr8:12188356 | A | G | 11 | a0002c0002t0001g0076 a0005c0007t0004g0028 a0005c0007t0004g0031 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+1452T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188356 | |||||||
| chr8:12188426 | T | TA | 6 | a0001c0001t0002g0036 a0003c0004t0001g0046 a0004c0006t0001g0044 others(3): Show |
6 | HG02109.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+1381dupT | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188426 | |||||||
| chr8:12188432 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1376T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188432 | |||||||
| chr8:12188433 | A | G | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.240+1375T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188433 | |||||||
| chr8:12188438 | T | A | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.240+1370A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188438 | |||||||
| chr8:12188459 | C | G | 4 | a0001c0024t0018g0035 a0007c0009t0003g0123 a0007c0009t0003g0124 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+1349G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188459 | |||||||
| chr8:12188464 | T | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1344A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188464 | |||||||
| chr8:12188473 | T | C | 19 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0126 others(16): Show |
19 | HG01070.hp2 HG01257.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.240+1335A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188473 | |||||||
| chr8:12188478 | A | G | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.240+1330T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188478 | |||||||
| chr8:12188485 | G | T | 1 | a0011c0013t0010g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.240+1323C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188485 | |||||||
| chr8:12188490 | G | C | 8 | a0001c0001t0002g0020 a0001c0001t0003g0116 a0001c0001t0003g0122 others(5): Show |
9 | HG01993.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+1318C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188490 | |||||||
| chr8:12188497 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1311A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188497 | |||||||
| chr8:12188506 | G | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+1302C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188506 | |||||||
| chr8:12188514 | T | G | 5 | a0001c0001t0002g0133 a0009c0011t0005g0026 a0009c0011t0005g0027 others(2): Show |
5 | HG01070.hp2 HG01257.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1294A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188514 | |||||||
| chr8:12188524 | G | A | 1 | a0002c0002t0001g0089 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.240+1284C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188524 | |||||||
| chr8:12188535 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+1273G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188535 | |||||||
| chr8:12188543 | C | G | 3 | a0005c0012t0004g0030 a0011c0013t0008g0025 a0011c0013t0010g0033 |
3 | HG03139.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+1265G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188543 | |||||||
| chr8:12188571 | G | C | 1 | a0010c0018t0001g0017 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.240+1237C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188571 | |||||||
| chr8:12188591 | G | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+1217C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188591 | |||||||
| chr8:12188611 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1197G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188611 | |||||||
| chr8:12188634 | CTG | C | 3 | a0006c0008t0001g0012 a0006c0008t0001g0058 a0006c0008t0001g0059 |
4 | HG00642.hp1 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+1172_240+1173d others(4): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188634 | |||||||
| chr8:12188641 | G | T | 28 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0126 others(25): Show |
34 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.240+1167C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188641 | |||||||
| chr8:12188644 | G | A | 7 | a0005c0007t0004g0031 a0005c0007t0004g0032 a0005c0007t0009g0024 others(4): Show |
7 | HG02486.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+1164C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188644 | |||||||
| chr8:12188697 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+1111T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188697 | |||||||
| chr8:12188704 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1104C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188704 | |||||||
| chr8:12188705 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1103C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188705 | |||||||
| chr8:12188710 | A | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1098T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188710 | |||||||
| chr8:12188725 | G | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+1083C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188725 | |||||||
| chr8:12188752 | G | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+1056C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188752 | |||||||
| chr8:12188776 | G | A | 1 | a0007c0009t0003g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.240+1032C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188776 | |||||||
| chr8:12188784 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1024C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188784 | |||||||
| chr8:12188786 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+1022C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188786 | |||||||
| chr8:12188792 | C | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+1016G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188792 | |||||||
| chr8:12188805 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+1003T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188805 | |||||||
| chr8:12188818 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+990C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188818 | |||||||
| chr8:12188821 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+987C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188821 | |||||||
| chr8:12188832 | A | T | 1 | a0003c0004t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.240+976T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188832 | |||||||
| chr8:12188844 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+964A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188844 | |||||||
| chr8:12188852 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+956A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188852 | |||||||
| chr8:12188854 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+954T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188854 | |||||||
| chr8:12188865 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+943G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188865 | |||||||
| chr8:12188898 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+910T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188898 | |||||||
| chr8:12188901 | A | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+907T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188901 | |||||||
| chr8:12188903 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+905A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188903 | |||||||
| chr8:12188909 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+899G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188909 | |||||||
| chr8:12188914 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+894G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188914 | |||||||
| chr8:12188924 | T | C | 1 | a0019c0027t0017g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.240+884A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188924 | |||||||
| chr8:12188937 | G | A | 5 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+871C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188937 | |||||||
| chr8:12188939 | T | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+869A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188939 | |||||||
| chr8:12188949 | C | A | 2 | a0007c0009t0003g0123 a0007c0009t0003g0124 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.240+859G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188949 | |||||||
| chr8:12188967 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+841C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188967 | |||||||
| chr8:12188976 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+832C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12188976 | |||||||
| chr8:12189021 | A | G | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+787T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189021 | |||||||
| chr8:12189050 | T | C | 12 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(9): Show |
13 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.240+758A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189050 | |||||||
| chr8:12189051 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+757C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189051 | |||||||
| chr8:12189059 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+749G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189059 | |||||||
| chr8:12189059 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+749G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189059 | |||||||
| chr8:12189074 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+734A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189074 | |||||||
| chr8:12189099 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+709G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189099 | |||||||
| chr8:12189101 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+707T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189101 | |||||||
| chr8:12189102 | A | C | 1 | a0005c0007t0004g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.240+706T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189102 | |||||||
| chr8:12189102 | A | G | 9 | a0005c0007t0004g0031 a0005c0007t0004g0032 a0005c0007t0009g0024 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+706T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189102 | |||||||
| chr8:12189107 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+701T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189107 | |||||||
| chr8:12189109 | A | G | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+699T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189109 | |||||||
| chr8:12189117 | A | G | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+691T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189117 | |||||||
| chr8:12189139 | TTAGCAGG others(1): Show |
T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+661_240+668del others(8): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189139 | |||||||
| chr8:12189159 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+649T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189159 | |||||||
| chr8:12189160 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+648G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189160 | |||||||
| chr8:12189169 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+639G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189169 | |||||||
| chr8:12189178 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+630G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189178 | |||||||
| chr8:12189190 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+618A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189190 | |||||||
| chr8:12189195 | C | T | 2 | a0012c0014t0007g0009 a0014c0022t0020g0132 |
3 | HG01884.hp1 NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+613G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189195 | |||||||
| chr8:12189199 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+609T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189199 | |||||||
| chr8:12189208 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+600G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189208 | |||||||
| chr8:12189209 | A | G | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+599T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189209 | |||||||
| chr8:12189223 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+585C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189223 | |||||||
| chr8:12189225 | C | T | 2 | a0007c0009t0003g0123 a0007c0009t0003g0124 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.240+583G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189225 | |||||||
| chr8:12189227 | A | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+581T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189227 | |||||||
| chr8:12189237 | ACT | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+569_240+570del others(2): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189237 | |||||||
| chr8:12189250 | AAAAATAT others(18): Show |
A | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.240+533_240+557del others(25): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189250 | |||||||
| chr8:12189250 | AAAAATAT others(30): Show |
A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+521_240+557del others(37): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189250 | |||||||
| chr8:12189251 | AAAATATA others(1): Show |
A | 4 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0084 others(1): Show |
6 | HG01257.hp2 HG01433.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+549_240+556del others(8): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189251 | |||||||
| chr8:12189251 | AAAATATA others(5): Show |
A | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+545_240+556del others(12): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189251 | |||||||
| chr8:12189257 | TATAA | T | 20 | a0001c0023t0001g0067 a0002c0002t0001g0001 a0002c0002t0001g0005 others(17): Show |
23 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.240+547_240+550del others(4): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189257 | |||||||
| chr8:12189257 | TATAAATA others(1): Show |
T | 30 | a0001c0001t0002g0018 a0001c0001t0002g0045 a0002c0002t0001g0001 others(27): Show |
42 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.240+543_240+550del others(8): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189257 | |||||||
| chr8:12189257 | TATAAATA others(5): Show |
T | 1 | a0006c0008t0001g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.240+539_240+550del others(12): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189257 | |||||||
| chr8:12189257 | TATAAATA others(9): Show |
T | 15 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(12): Show |
16 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.240+535_240+550del others(16): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189257 | |||||||
| chr8:12189257 | TATAAATA others(13): Show |
T | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.240+531_240+550del others(20): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189257 | |||||||
| chr8:12189265 | A | T | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+543T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189265 | |||||||
| chr8:12189286 | A | G | 1 | a0017c0030t0019g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.240+522T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189286 | |||||||
| chr8:12189287 | TAAATAAA others(10): Show |
T | 1 | a0017c0030t0019g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.240+504_240+520del others(17): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189287 | |||||||
| chr8:12189290 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+518T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189290 | |||||||
| chr8:12189290 | ATAAATAA others(5): Show |
A | 1 | a0001c0001t0002g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.240+506_240+517del others(12): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189290 | |||||||
| chr8:12189291 | T | C | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+517A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189291 | |||||||
| chr8:12189294 | ATAAATAA others(1): Show |
A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(30): Show |
42 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.240+506_240+513del others(8): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189294 | |||||||
| chr8:12189298 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+510T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189298 | |||||||
| chr8:12189298 | ATAAG | A | 8 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(5): Show |
12 | HG00323.hp2 HG01884.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.240+506_240+509del others(4): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189298 | |||||||
| chr8:12189323 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+485T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189323 | |||||||
| chr8:12189363 | A | G | 2 | a0001c0024t0018g0035 a0014c0022t0020g0132 |
2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.240+445T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189363 | |||||||
| chr8:12189405 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.240+403C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189405 | |||||||
| chr8:12189411 | A | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+397T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189411 | |||||||
| chr8:12189432 | G | A | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+376C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189432 | |||||||
| chr8:12189438 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+370G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189438 | |||||||
| chr8:12189446 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+362C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189446 | |||||||
| chr8:12189447 | G | A | 1 | a0001c0001t0003g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.240+361C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189447 | |||||||
| chr8:12189474 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+334A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189474 | |||||||
| chr8:12189477 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+331A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189477 | |||||||
| chr8:12189482 | A | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+326T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189482 | |||||||
| chr8:12189483 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+325C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189483 | |||||||
| chr8:12189485 | A | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+323T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189485 | |||||||
| chr8:12189492 | G | T | 8 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0120 others(5): Show |
9 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+316C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189492 | |||||||
| chr8:12189502 | T | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+306A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189502 | |||||||
| chr8:12189515 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+293C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189515 | |||||||
| chr8:12189516 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+292A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189516 | |||||||
| chr8:12189522 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+286C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189522 | |||||||
| chr8:12189524 | T | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+284A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189524 | |||||||
| chr8:12189532 | G | A | 1 | a0002c0003t0001g0090 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.240+276C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189532 | |||||||
| chr8:12189535 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+273T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189535 | |||||||
| chr8:12189547 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+261G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189547 | |||||||
| chr8:12189550 | T | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+258A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189550 | |||||||
| chr8:12189553 | G | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+255C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189553 | |||||||
| chr8:12189554 | C | G | 1 | a0008c0016t0002g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.240+254G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189554 | |||||||
| chr8:12189564 | A | G | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+244T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189564 | |||||||
| chr8:12189574 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+234C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189574 | |||||||
| chr8:12189592 | A | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+216T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189592 | |||||||
| chr8:12189599 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+209T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189599 | |||||||
| chr8:12189600 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+208C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189600 | |||||||
| chr8:12189607 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+201G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189607 | |||||||
| chr8:12189609 | C | G | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
12 | HG00642.hp1 HG01175.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.240+199G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189609 | |||||||
| chr8:12189613 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+195C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189613 | |||||||
| chr8:12189619 | T | C | 45 | a0001c0005t0002g0111 a0002c0002t0001g0001 a0002c0002t0001g0004 others(42): Show |
65 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.240+189A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189619 | |||||||
| chr8:12189634 | A | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+174T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189634 | |||||||
| chr8:12189668 | T | A | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+140A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189668 | |||||||
| chr8:12189671 | G | C | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.240+137C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189671 | |||||||
| chr8:12189689 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+119C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189689 | |||||||
| chr8:12189691 | G | A | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.240+117C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189691 | |||||||
| chr8:12189695 | G | C | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+113C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189695 | |||||||
| chr8:12189701 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+107G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189701 | |||||||
| chr8:12189707 | T | C | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+101A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189707 | |||||||
| chr8:12189708 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.240+100C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189708 | |||||||
| chr8:12189743 | C | T | 31 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(28): Show |
51 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.240+65G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189743 | |||||||
| chr8:12189744 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+64C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189744 | |||||||
| chr8:12189746 | A | G | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+62T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189746 | |||||||
| chr8:12189748 | T | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+60A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189748 | |||||||
| chr8:12189749 | G | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+59C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189749 | |||||||
| chr8:12189750 | T | C | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+58A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189750 | |||||||
| chr8:12189751 | G | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+57C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189751 | |||||||
| chr8:12189754 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+54C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189754 | |||||||
| chr8:12189755 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+53G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189755 | |||||||
| chr8:12189758 | G | A | 59 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(56): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.240+50C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189758 | |||||||
| chr8:12189760 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+48G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189760 | |||||||
| chr8:12189776 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+32G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189776 | |||||||
| chr8:12189777 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+31T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189777 | |||||||
| chr8:12189787 | C | T | 1 | a0008c0016t0002g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.240+21G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189787 | |||||||
| chr8:12189791 | C | T | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.240+17G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189791 | |||||||
| chr8:12189798 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+10A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189798 | |||||||
| chr8:12189801 | A | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.240+7T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189801 | |||||||
| chr8:12189807 | C | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(38): Show |
54 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
splice_donor_variant&intron_variant | HIGH | c.240+1G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 3/6 | chr8 | 12189807 | |||||||
| chr8:12189893 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.160-5C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189893 | |||||||
| chr8:12189916 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-28G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189916 | |||||||
| chr8:12189918 | T | C | 11 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(8): Show |
12 | HG01070.hp2 HG01257.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.160-30A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189918 | |||||||
| chr8:12189929 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-41G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189929 | |||||||
| chr8:12189930 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-42A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189930 | |||||||
| chr8:12189931 | TAAGTCTC | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-50_160-44delGA others(5): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189931 | |||||||
| chr8:12189987 | A | G | 32 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(29): Show |
52 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.160-99T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189987 | |||||||
| chr8:12189998 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-110T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12189998 | |||||||
| chr8:12190022 | T | C | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-134A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190022 | |||||||
| chr8:12190026 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-138G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190026 | |||||||
| chr8:12190030 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-142A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190030 | |||||||
| chr8:12190060 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-172G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190060 | |||||||
| chr8:12190071 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-183T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190071 | |||||||
| chr8:12190114 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-226A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190114 | |||||||
| chr8:12190165 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-277G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190165 | |||||||
| chr8:12190188 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-300C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190188 | |||||||
| chr8:12190190 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-302A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190190 | |||||||
| chr8:12190201 | G | C | 1 | a0007c0009t0003g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160-313C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190201 | |||||||
| chr8:12190202 | T | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-314A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190202 | |||||||
| chr8:12190236 | G | A | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-348C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190236 | |||||||
| chr8:12190239 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-351T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190239 | |||||||
| chr8:12190246 | A | G | 1 | a0010c0018t0001g0017 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160-358T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190246 | |||||||
| chr8:12190260 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-372G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190260 | |||||||
| chr8:12190267 | A | G | 1 | a0001c0001t0003g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.160-379T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190267 | |||||||
| chr8:12190321 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-433T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190321 | |||||||
| chr8:12190329 | C | T | 17 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(14): Show |
18 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.160-441G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190329 | |||||||
| chr8:12190337 | G | A | 1 | a0017c0030t0019g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.160-449C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190337 | |||||||
| chr8:12190369 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-481C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190369 | |||||||
| chr8:12190401 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-513G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190401 | |||||||
| chr8:12190402 | G | A | 11 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0005t0002g0109 others(8): Show |
14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-514C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190402 | |||||||
| chr8:12190408 | G | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-520C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190408 | |||||||
| chr8:12190418 | C | T | 4 | a0006c0008t0001g0012 a0006c0008t0001g0058 a0006c0008t0001g0059 others(1): Show |
5 | HG00642.hp1 HG01175.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-530G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190418 | |||||||
| chr8:12190436 | G | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-548C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190436 | |||||||
| chr8:12190438 | G | T | 1 | a0001c0001t0003g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-550C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190438 | |||||||
| chr8:12190448 | T | A | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160-560A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190448 | |||||||
| chr8:12190448 | T | G | 4 | a0006c0008t0001g0059 a0009c0011t0005g0026 a0009c0011t0005g0027 others(1): Show |
4 | HG01070.hp2 HG01175.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-560A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190448 | |||||||
| chr8:12190454 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-566G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190454 | |||||||
| chr8:12190457 | C | G | 1 | a0005c0007t0004g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160-569G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190457 | |||||||
| chr8:12190457 | C | T | 9 | a0005c0007t0004g0031 a0005c0007t0004g0032 a0005c0007t0009g0024 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-569G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190457 | |||||||
| chr8:12190460 | G | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-572C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190460 | |||||||
| chr8:12190468 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-580C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190468 | |||||||
| chr8:12190492 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-604G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190492 | |||||||
| chr8:12190493 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-605G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190493 | |||||||
| chr8:12190493 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-605G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190493 | |||||||
| chr8:12190497 | C | T | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-609G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190497 | |||||||
| chr8:12190502 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-614G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190502 | |||||||
| chr8:12190528 | T | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-640A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190528 | |||||||
| chr8:12190535 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-647G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190535 | |||||||
| chr8:12190544 | C | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-656G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190544 | |||||||
| chr8:12190556 | G | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-668C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190556 | |||||||
| chr8:12190580 | G | A | 1 | a0002c0026t0003g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.160-692C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190580 | |||||||
| chr8:12190581 | T | G | 130 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(127): Show |
172 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.160-693A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190581 | |||||||
| chr8:12190585 | T | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-697A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190585 | |||||||
| chr8:12190596 | T | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-708A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190596 | |||||||
| chr8:12190598 | G | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-710C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190598 | |||||||
| chr8:12190604 | ACC | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-718_160-717del others(2): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190604 | |||||||
| chr8:12190609 | G | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-721C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190609 | |||||||
| chr8:12190616 | G | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-728C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190616 | |||||||
| chr8:12190633 | G | A | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-745C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190633 | |||||||
| chr8:12190652 | T | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-764A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190652 | |||||||
| chr8:12190661 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-773A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190661 | |||||||
| chr8:12190671 | A | G | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-783T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190671 | |||||||
| chr8:12190683 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-795G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190683 | |||||||
| chr8:12190699 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-811G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190699 | |||||||
| chr8:12190714 | A | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-826T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190714 | |||||||
| chr8:12190730 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-842C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190730 | |||||||
| chr8:12190742 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-854T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190742 | |||||||
| chr8:12190751 | AT | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-864delA | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190751 | |||||||
| chr8:12190761 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-873T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190761 | |||||||
| chr8:12190786 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.160-898G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190786 | |||||||
| chr8:12190792 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-904C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190792 | |||||||
| chr8:12190812 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-924G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190812 | |||||||
| chr8:12190814 | T | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-926A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190814 | |||||||
| chr8:12190829 | C | T | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-941G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190829 | |||||||
| chr8:12190830 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.160-942C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190830 | |||||||
| chr8:12190849 | A | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+930T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190849 | |||||||
| chr8:12190851 | A | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+928T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190851 | |||||||
| chr8:12190854 | T | G | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+925A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190854 | |||||||
| chr8:12190856 | GGATTACA others(3): Show |
G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+913_159+922del others(10): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190856 | |||||||
| chr8:12190877 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+902T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190877 | |||||||
| chr8:12190880 | A | C | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+899T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190880 | |||||||
| chr8:12190892 | C | G | 31 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(28): Show |
51 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.159+887G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190892 | |||||||
| chr8:12190912 | C | G | 15 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(12): Show |
16 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.159+867G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190912 | |||||||
| chr8:12190938 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+841A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190938 | |||||||
| chr8:12190964 | A | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
87 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.159+815T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190964 | |||||||
| chr8:12190970 | A | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.159+809T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190970 | |||||||
| chr8:12190975 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.159+804G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190975 | |||||||
| chr8:12190999 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.159+780C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12190999 | |||||||
| chr8:12191021 | A | C | 1 | a0001c0001t0002g0066 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.159+758T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191021 | |||||||
| chr8:12191028 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.159+751G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191028 | |||||||
| chr8:12191029 | G | A | 8 | a0002c0003t0001g0063 a0002c0003t0001g0064 a0005c0007t0004g0028 others(5): Show |
8 | HG00423.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+750C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191029 | |||||||
| chr8:12191029 | G | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.159+750C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191029 | |||||||
| chr8:12191031 | A | G | 1 | a0008c0016t0002g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.159+748T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191031 | |||||||
| chr8:12191063 | C | T | 58 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(55): Show |
84 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.159+716G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191063 | |||||||
| chr8:12191082 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+697A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191082 | |||||||
| chr8:12191088 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.159+691C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191088 | |||||||
| chr8:12191106 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+673C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191106 | |||||||
| chr8:12191136 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+643G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191136 | |||||||
| chr8:12191155 | C | T | 1 | a0001c0001t0003g0115 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.159+624G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191155 | |||||||
| chr8:12191178 | A | ATTC | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+598_159+600dup others(3): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191178 | |||||||
| chr8:12191226 | A | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+553T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191226 | |||||||
| chr8:12191240 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.159+539G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191240 | |||||||
| chr8:12191245 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+534A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191245 | |||||||
| chr8:12191257 | C | T | 1 | a0010c0018t0001g0017 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.159+522G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191257 | |||||||
| chr8:12191292 | T | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+487A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191292 | |||||||
| chr8:12191302 | A | C | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+477T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191302 | |||||||
| chr8:12191304 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+475G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191304 | |||||||
| chr8:12191309 | G | A | 16 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(13): Show |
17 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.159+470C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191309 | |||||||
| chr8:12191316 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+463G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191316 | |||||||
| chr8:12191318 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+461T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191318 | |||||||
| chr8:12191320 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+459C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191320 | |||||||
| chr8:12191325 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.159+454C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191325 | |||||||
| chr8:12191340 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+439A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191340 | |||||||
| chr8:12191365 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+414T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191365 | |||||||
| chr8:12191388 | G | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+391C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191388 | |||||||
| chr8:12191401 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+378G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191401 | |||||||
| chr8:12191406 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+373T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191406 | |||||||
| chr8:12191415 | A | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.159+364T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191415 | |||||||
| chr8:12191429 | G | T | 31 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(28): Show |
51 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.159+350C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191429 | |||||||
| chr8:12191465 | T | C | 62 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(59): Show |
89 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.159+314A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191465 | |||||||
| chr8:12191513 | T | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+266A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191513 | |||||||
| chr8:12191521 | T | A | 1 | a0019c0027t0017g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.159+258A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191521 | |||||||
| chr8:12191543 | C | T | 1 | a0001c0015t0006g0013 | 2 | HG00323.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.159+236G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191543 | |||||||
| chr8:12191547 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+232G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191547 | |||||||
| chr8:12191558 | A | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+221T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191558 | |||||||
| chr8:12191573 | A | C | 1 | a0003c0004t0001g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.159+206T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191573 | |||||||
| chr8:12191580 | T | TG | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+198_159+199ins others(1): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191580 | |||||||
| chr8:12191592 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+187G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191592 | |||||||
| chr8:12191606 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+173G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191606 | |||||||
| chr8:12191607 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+172G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191607 | |||||||
| chr8:12191609 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+170A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191609 | |||||||
| chr8:12191615 | C | T | 1 | a0002c0002t0016g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.159+164G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191615 | |||||||
| chr8:12191620 | G | A | 1 | a0001c0005t0002g0111 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.159+159C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191620 | |||||||
| chr8:12191633 | C | A | 15 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(12): Show |
16 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.159+146G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191633 | |||||||
| chr8:12191633 | C | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.159+146G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191633 | |||||||
| chr8:12191636 | T | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+143A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191636 | |||||||
| chr8:12191637 | C | T | 18 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(15): Show |
19 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+142G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191637 | |||||||
| chr8:12191641 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+138T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191641 | |||||||
| chr8:12191672 | G | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+107C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191672 | |||||||
| chr8:12191675 | G | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+104C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191675 | |||||||
| chr8:12191676 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+103C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191676 | |||||||
| chr8:12191677 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+102G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191677 | |||||||
| chr8:12191691 | T | G | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+88A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191691 | |||||||
| chr8:12191704 | G | C | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159+75C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191704 | |||||||
| chr8:12191705 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+74A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191705 | |||||||
| chr8:12191707 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+72G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191707 | |||||||
| chr8:12191709 | G | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+70C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191709 | |||||||
| chr8:12191722 | C | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.159+57G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191722 | |||||||
| chr8:12191738 | A | G | 92 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(89): Show |
121 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.159+41T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191738 | |||||||
| chr8:12191747 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+32T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191747 | |||||||
| chr8:12191770 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+9C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 2/6 | chr8 | 12191770 | |||||||
| chr8:12191851 | T | C | 4 | a0009c0011t0005g0026 a0009c0011t0005g0027 a0011c0013t0008g0025 others(1): Show |
4 | HG01070.hp2 HG01257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-10A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12191851 | |||||||
| chr8:12191876 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-35G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12191876 | |||||||
| chr8:12191892 | T | TA | 9 | a0005c0007t0004g0031 a0005c0007t0004g0032 a0005c0007t0009g0024 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-52dupT | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12191892 | |||||||
| chr8:12191899 | G | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-58C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12191899 | |||||||
| chr8:12192006 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-165C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192006 | |||||||
| chr8:12192010 | C | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-169G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192010 | |||||||
| chr8:12192047 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-206A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192047 | |||||||
| chr8:12192048 | C | A | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-207G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192048 | |||||||
| chr8:12192067 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-226G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192067 | |||||||
| chr8:12192071 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-230A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192071 | |||||||
| chr8:12192079 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-238T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192079 | |||||||
| chr8:12192103 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-262T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192103 | |||||||
| chr8:12192113 | G | T | 1 | a0005c0012t0004g0029 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.97-272C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192113 | |||||||
| chr8:12192127 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-286C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192127 | |||||||
| chr8:12192129 | G | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-288C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192129 | |||||||
| chr8:12192206 | G | A | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-365C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192206 | |||||||
| chr8:12192216 | T | C | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-375A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192216 | |||||||
| chr8:12192237 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-396G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192237 | |||||||
| chr8:12192238 | C | A | 16 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(13): Show |
17 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-397G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192238 | |||||||
| chr8:12192245 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-404A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192245 | |||||||
| chr8:12192246 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-405C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192246 | |||||||
| chr8:12192251 | T | G | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-410A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192251 | |||||||
| chr8:12192259 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-418G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192259 | |||||||
| chr8:12192296 | T | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-455A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192296 | |||||||
| chr8:12192297 | G | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-456C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192297 | |||||||
| chr8:12192298 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-457C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192298 | |||||||
| chr8:12192306 | C | T | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-465G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192306 | |||||||
| chr8:12192326 | T | G | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-485A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192326 | |||||||
| chr8:12192329 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-488A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192329 | |||||||
| chr8:12192333 | C | A | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.97-492G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192333 | |||||||
| chr8:12192345 | C | T | 1 | a0005c0007t0009g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.97-504G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192345 | |||||||
| chr8:12192352 | G | A | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-511C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192352 | |||||||
| chr8:12192357 | C | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-516G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192357 | |||||||
| chr8:12192359 | G | C | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-518C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192359 | |||||||
| chr8:12192368 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-527G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192368 | |||||||
| chr8:12192377 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-536G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192377 | |||||||
| chr8:12192380 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-539C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192380 | |||||||
| chr8:12192391 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-550G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192391 | |||||||
| chr8:12192393 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-552T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192393 | |||||||
| chr8:12192403 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-562G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192403 | |||||||
| chr8:12192422 | C | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-581G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192422 | |||||||
| chr8:12192433 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-592C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192433 | |||||||
| chr8:12192439 | C | G | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-598G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192439 | |||||||
| chr8:12192444 | G | T | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-603C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192444 | |||||||
| chr8:12192466 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-625T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192466 | |||||||
| chr8:12192474 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-633T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192474 | |||||||
| chr8:12192493 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-652A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192493 | |||||||
| chr8:12192538 | T | C | 31 | a0001c0001t0002g0114 a0001c0001t0003g0023 a0001c0001t0003g0115 others(28): Show |
33 | HG01070.hp2 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.97-697A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192538 | |||||||
| chr8:12192561 | TG | T | 3 | a0001c0001t0002g0095 a0005c0007t0004g0028 a0011c0013t0008g0025 |
3 | HG02109.hp2 NA18994.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97-721delC | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192561 | |||||||
| chr8:12192584 | T | C | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-743A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192584 | |||||||
| chr8:12192597 | A | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-756T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192597 | |||||||
| chr8:12192598 | G | C | 131 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(128): Show |
172 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.97-757C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192598 | |||||||
| chr8:12192622 | C | A | 1 | a0010c0018t0001g0017 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97-781G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192622 | |||||||
| chr8:12192626 | T | C | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-785A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192626 | |||||||
| chr8:12192636 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-795T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192636 | |||||||
| chr8:12192680 | A | ATTTATTT others(1): Show |
10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-840_97-839insCA others(6): Show |
FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192680 | |||||||
| chr8:12192692 | T | G | 122 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(119): Show |
164 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.97-851A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192692 | |||||||
| chr8:12192734 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-893G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192734 | |||||||
| chr8:12192747 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-906G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192747 | |||||||
| chr8:12192755 | C | T | 4 | a0002c0017t0002g0038 a0003c0004t0001g0010 a0003c0004t0001g0039 others(1): Show |
5 | HG00642.hp2 HG01106.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-914G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192755 | |||||||
| chr8:12192756 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-915C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192756 | |||||||
| chr8:12192786 | A | AG | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-946_97-945insC | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192786 | |||||||
| chr8:12192787 | A | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-946T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192787 | |||||||
| chr8:12192788 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-947C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192788 | |||||||
| chr8:12192788 | G | T | 1 | a0017c0030t0019g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97-947C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192788 | |||||||
| chr8:12192812 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-971C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192812 | |||||||
| chr8:12192812 | G | T | 1 | a0003c0004t0001g0057 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.97-971C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192812 | |||||||
| chr8:12192840 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-999C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192840 | |||||||
| chr8:12192846 | A | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1005T>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192846 | |||||||
| chr8:12192848 | T | C | 2 | a0009c0011t0005g0026 a0009c0011t0005g0027 |
2 | HG01070.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.97-1007A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192848 | |||||||
| chr8:12192858 | C | T | 17 | a0001c0001t0003g0023 a0001c0001t0003g0115 a0001c0001t0003g0116 others(14): Show |
18 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-1017G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192858 | |||||||
| chr8:12192864 | G | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1023C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192864 | |||||||
| chr8:12192896 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1055G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192896 | |||||||
| chr8:12192897 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1056G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192897 | |||||||
| chr8:12192907 | T | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1066A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192907 | |||||||
| chr8:12192921 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1054A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192921 | |||||||
| chr8:12192935 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1040T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12192935 | |||||||
| chr8:12193026 | T | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+949A>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193026 | |||||||
| chr8:12193084 | G | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+891C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193084 | |||||||
| chr8:12193120 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+855A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193120 | |||||||
| chr8:12193125 | G | T | 5 | a0002c0003t0001g0060 a0002c0003t0001g0061 a0002c0003t0001g0062 others(2): Show |
5 | HG00423.hp2 HG02148.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+850C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193125 | |||||||
| chr8:12193205 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+770G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193205 | |||||||
| chr8:12193207 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+768G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193207 | |||||||
| chr8:12193244 | T | C | 1 | a0003c0004t0001g0057 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.96+731A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193244 | |||||||
| chr8:12193252 | G | A | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.96+723C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193252 | |||||||
| chr8:12193265 | C | T | 18 | a0001c0001t0002g0114 a0001c0001t0003g0023 a0001c0001t0003g0115 others(15): Show |
19 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+710G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193265 | |||||||
| chr8:12193266 | A | G | 30 | a0001c0001t0002g0114 a0001c0001t0003g0023 a0001c0001t0003g0115 others(27): Show |
32 | HG01070.hp2 HG01081.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+709T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193266 | |||||||
| chr8:12193267 | C | A | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.96+708G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193267 | |||||||
| chr8:12193324 | C | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
49 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.96+651G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193324 | |||||||
| chr8:12193335 | T | TC | 9 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(6): Show |
9 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+639dupG | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193335 | |||||||
| chr8:12193348 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+627T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193348 | |||||||
| chr8:12193370 | A | G | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+605T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193370 | |||||||
| chr8:12193371 | C | T | 1 | a0018c0028t0001g0037 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.96+604G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193371 | |||||||
| chr8:12193377 | G | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+598C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193377 | |||||||
| chr8:12193409 | T | G | 3 | a0006c0008t0001g0012 a0006c0008t0001g0058 a0006c0008t0001g0059 |
4 | HG00642.hp1 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+566A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193409 | |||||||
| chr8:12193413 | G | A | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+562C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193413 | |||||||
| chr8:12193418 | C | A | 3 | a0002c0026t0003g0113 a0011c0013t0008g0025 a0011c0013t0010g0033 |
3 | HG03209.hp1 NA19077.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.96+557G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193418 | |||||||
| chr8:12193452 | G | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.96+523C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193452 | |||||||
| chr8:12193457 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.96+518C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193457 | |||||||
| chr8:12193467 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+508G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193467 | |||||||
| chr8:12193478 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+497C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193478 | |||||||
| chr8:12193502 | G | C | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.96+473C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193502 | |||||||
| chr8:12193518 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+457G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193518 | |||||||
| chr8:12193525 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+450C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193525 | |||||||
| chr8:12193528 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+447G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193528 | |||||||
| chr8:12193551 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.96+424T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193551 | |||||||
| chr8:12193561 | A | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+414T>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193561 | |||||||
| chr8:12193563 | G | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+412C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193563 | |||||||
| chr8:12193575 | G | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+400C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193575 | |||||||
| chr8:12193589 | G | A | 20 | a0001c0001t0002g0114 a0001c0001t0003g0023 a0001c0001t0003g0115 others(17): Show |
21 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+386C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193589 | |||||||
| chr8:12193589 | G | T | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+386C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193589 | |||||||
| chr8:12193601 | A | G | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+374T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193601 | |||||||
| chr8:12193610 | C | A | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+365G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193610 | |||||||
| chr8:12193612 | C | T | 27 | a0001c0001t0002g0045 a0002c0003t0001g0047 a0002c0017t0002g0038 others(24): Show |
33 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.96+363G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193612 | |||||||
| chr8:12193615 | G | C | 1 | a0009c0011t0005g0027 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.96+360C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193615 | |||||||
| chr8:12193650 | T | C | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.96+325A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193650 | |||||||
| chr8:12193650 | T | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+325A>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193650 | |||||||
| chr8:12193655 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+320G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193655 | |||||||
| chr8:12193661 | C | G | 6 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+314G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193661 | |||||||
| chr8:12193697 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+278C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193697 | |||||||
| chr8:12193715 | C | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+260G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193715 | |||||||
| chr8:12193727 | G | C | 130 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(127): Show |
171 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.96+248C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193727 | |||||||
| chr8:12193732 | G | C | 1 | a0002c0002t0001g0131 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.96+243C>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193732 | |||||||
| chr8:12193740 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+235T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193740 | |||||||
| chr8:12193742 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+233G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193742 | |||||||
| chr8:12193745 | C | G | 1 | a0012c0014t0007g0009 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.96+230G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193745 | |||||||
| chr8:12193746 | T | C | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
11 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+229A>G | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193746 | |||||||
| chr8:12193750 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+225C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193750 | |||||||
| chr8:12193752 | G | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+223C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193752 | |||||||
| chr8:12193773 | C | T | 8 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+202G>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193773 | |||||||
| chr8:12193778 | C | A | 2 | a0011c0013t0008g0025 a0011c0013t0010g0033 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.96+197G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193778 | |||||||
| chr8:12193794 | A | G | 11 | a0001c0001t0002g0036 a0005c0007t0004g0028 a0005c0007t0004g0031 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+181T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193794 | |||||||
| chr8:12193796 | G | T | 11 | a0001c0001t0002g0036 a0005c0007t0004g0028 a0005c0007t0004g0031 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+179C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193796 | |||||||
| chr8:12193799 | G | A | 1 | a0014c0022t0020g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+176C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193799 | |||||||
| chr8:12193802 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+173G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193802 | |||||||
| chr8:12193825 | G | T | 1 | a0001c0024t0018g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.96+150C>A | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193825 | |||||||
| chr8:12193856 | G | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+119C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193856 | |||||||
| chr8:12193857 | A | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+118T>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193857 | |||||||
| chr8:12193882 | C | A | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+93G>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193882 | |||||||
| chr8:12193932 | TC | T | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+42delG | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193932 | |||||||
| chr8:12193940 | C | G | 10 | a0005c0007t0004g0028 a0005c0007t0004g0031 a0005c0007t0004g0032 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+35G>C | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193940 | |||||||
| chr8:12193966 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.96+9C>T | FAM86B1 | ENSG00000186523.15 | transcript | ENST00000448228.7 | protein_coding | 1/6 | chr8 | 12193966 |