Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 222584 |
| ensemblid | ENSG00000168143.9 |
| hgncid | 21357 |
| symbol | FAM83B |
| name | family with sequence similarity 83 member B |
| refseq_nuc | NM_001010872.3 |
| refseq_prot | NP_001010872.1 |
| ensembl_nuc | ENST00000306858.8 |
| ensembl_prot | ENSP00000304078.7 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 54846771 |
| end | 54945099 |
| strand | + |
| ver | v1.2 |
| region | chr6:54846771-54945099 |
| region5000 | chr6:54841771-54950099 |
| regionname0 | FAM83B_chr6_54846771_54945099 |
| regionname5000 | FAM83B_chr6_54841771_54950099 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1011 | 174 | 19 | 43 | 78 | 3 | 29 | 58 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0002 | 0/0 | 1011 | 60 | 37 | 11 | 5 | 3 | 4 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0003 | 0/0 | 1011 | 22 | 22 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0004 | 0/0 | 1011 | 10 | 8 | 1 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0005 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0006 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0007 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| a0009 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | METSS others(1006): Show |
chr6 | 54841771 | 54950099 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3033 | 92 | 10 | 23 | 41 | 2 | 15 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0001c0002 | 0/1 | 3033 | 66 | 6 | 20 | 26 | 1 | 12 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0001c0008 | 0/0 | 3033 | 8 | 0 | 0 | 7 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0001c0012 | 0/0 | 3033 | 3 | 2 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0001c0013 | 0/0 | 3033 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0001c0021 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0001c0022 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0003 | 0/0 | 3033 | 23 | 13 | 6 | 0 | 1 | 3 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0004 | 0/0 | 3033 | 13 | 8 | 0 | 4 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0005 | 0/0 | 3033 | 10 | 9 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0009 | 0/0 | 3033 | 6 | 3 | 3 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0010 | 0/0 | 3033 | 5 | 2 | 2 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0023 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0026 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0002c0028 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0003c0006 | 0/0 | 3033 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0003c0007 | 0/0 | 3033 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0003c0016 | 0/0 | 3033 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0003c0017 | 0/0 | 3033 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0004c0011 | 0/0 | 3033 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0004c0014 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0004c0018 | 0/0 | 3033 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0004c0024 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0005c0015 | 0/0 | 3033 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0006c0027 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0007c0025 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0008c0020 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 | ||
| a0009c0019 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | ATGGA others(3028): Show |
chr6 | 54841771 | 54950099 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6244 | 65 | 1 | 12 | 38 | 2 | 12 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0002 | 1/0 | 6244 | 6 | 1 | 0 | 2 | 0 | 2 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0004 | 0/0 | 6245 | 12 | 2 | 10 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0010 | 0/0 | 6244 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0023 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0024 | 0/0 | 6244 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0034 | 0/0 | 6245 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0001c0001t0035 | 0/0 | 6244 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0002t0001 | 0/0 | 6244 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0002t0002 | 0/1 | 6244 | 57 | 6 | 20 | 19 | 1 | 10 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0002t0014 | 0/0 | 6244 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0002t0015 | 0/0 | 6244 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0002t0021 | 0/0 | 6244 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0008t0005 | 0/0 | 6244 | 7 | 0 | 0 | 6 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0008t0025 | 0/0 | 6244 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0012t0001 | 0/0 | 6244 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0012t0002 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0012t0008 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0013t0005 | 0/0 | 6244 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0021t0005 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0001c0022t0001 | 0/0 | 6244 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0002c0003t0003 | 0/0 | 6245 | 21 | 11 | 6 | 0 | 1 | 3 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0002c0003t0016 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0002c0003t0026 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0002c0004t0003 | 0/0 | 6245 | 4 | 3 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0002c0004t0012 | 0/0 | 6245 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0002c0004t0020 | 0/0 | 6418 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6413): Show |
chr6 | 54841771 | 54950099 |
| a0002c0004t0030 | 0/0 | 6393 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6388): Show |
chr6 | 54841771 | 54950099 |
| a0002c0004t0032 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6410): Show |
chr6 | 54841771 | 54950099 |
| a0002c0004t0033 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0002c0005t0003 | 0/0 | 6245 | 3 | 2 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0002c0005t0013 | 0/0 | 6405 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6400): Show |
chr6 | 54841771 | 54950099 |
| a0002c0005t0018 | 0/0 | 6406 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6401): Show |
chr6 | 54841771 | 54950099 |
| a0002c0005t0019 | 0/0 | 6411 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6406): Show |
chr6 | 54841771 | 54950099 |
| a0002c0009t0011 | 0/0 | 6379 | 5 | 2 | 3 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6374): Show |
chr6 | 54841771 | 54950099 |
| a0002c0009t0029 | 0/0 | 6380 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6375): Show |
chr6 | 54841771 | 54950099 |
| a0002c0010t0009 | 0/0 | 6244 | 5 | 2 | 2 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0002c0023t0031 | 0/0 | 6401 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6396): Show |
chr6 | 54841771 | 54950099 |
| a0002c0026t0016 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0002c0028t0009 | 0/0 | 6244 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0003c0006t0007 | 0/0 | 6244 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0003c0007t0006 | 0/0 | 6244 | 8 | 8 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0003c0007t0028 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0003c0016t0007 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0003c0016t0027 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0003c0017t0006 | 0/0 | 6244 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0004c0011t0008 | 0/0 | 6244 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0004c0014t0002 | 0/0 | 6244 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0004c0018t0008 | 0/0 | 6244 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0004c0024t0008 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0005c0015t0017 | 0/0 | 6244 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0006c0027t0002 | 0/0 | 6244 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0007c0025t0003 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6240): Show |
chr6 | 54841771 | 54950099 |
| a0008c0020t0002 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| a0009c0019t0022 | 0/0 | 6244 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | AAACC others(6239): Show |
chr6 | 54841771 | 54950099 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0023g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0024g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0034g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0035g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0014g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0014g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0014g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0015g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0015g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0021g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0021g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0025g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0012t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0012t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0012t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0013t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0013t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0013t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0021t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0022t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0016g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0026g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0030g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0032g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0033g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0018g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0018g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0019g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0023t0031g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0026t0016g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0028t0009g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0028g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0016t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0016t0027g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0017t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0017t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0014t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0014t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0014t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0018t0008g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0018t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0024t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0005c0015t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0005c0015t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0006c0027t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0007c0025t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0008c0020t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0009c0019t0022g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0010 | t0009 | g0007 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0212 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00323 | hp1 | a0002 | c0028 | t0009 | g0188 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00438 | hp2 | a0002 | c0004 | t0012 | g0176 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00544 | hp1 | a0001 | c0008 | t0005 | g0016 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00642 | hp2 | a0002 | c0010 | t0009 | g0008 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00735 | hp1 | a0001 | c0001 | t0035 | g0022 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00741 | hp2 | a0002 | c0009 | t0011 | g0163 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0055 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0160 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01167 | hp2 | a0002 | c0009 | t0011 | g0249 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0037 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01169 | hp1 | a0002 | c0009 | t0011 | g0247 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01169 | hp2 | a0002 | c0003 | t0003 | g0027 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01175 | hp2 | a0004 | c0018 | t0008 | g0059 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0140 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01192 | hp2 | a0002 | c0003 | t0003 | g0053 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0021 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0226 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0162 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01361 | hp1 | a0002 | c0010 | t0009 | g0074 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0098 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01884 | hp1 | a0002 | c0010 | t0009 | g0069 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01884 | hp2 | a0002 | c0005 | t0013 | g0201 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01891 | hp1 | a0002 | c0005 | t0013 | g0225 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01891 | hp2 | a0002 | c0009 | t0029 | g0243 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01934 | hp1 | a0002 | c0003 | t0003 | g0038 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01978 | hp1 | a0006 | c0027 | t0002 | g0181 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02027 | hp1 | a0002 | c0004 | t0012 | g0179 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02132 | hp2 | a0002 | c0004 | t0012 | g0218 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02145 | hp1 | a0004 | c0011 | t0008 | g0263 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02165 | hp2 | a0001 | c0002 | t0021 | g0197 | EAS | CDX | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0200 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02257 | hp2 | a0004 | c0011 | t0008 | g0257 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02258 | hp1 | a0002 | c0005 | t0003 | g0017 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02258 | hp2 | a0002 | c0005 | t0003 | g0048 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02280 | hp1 | a0003 | c0006 | t0007 | g0166 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02280 | hp2 | a0002 | c0003 | t0003 | g0039 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02451 | hp2 | a0003 | c0007 | t0006 | g0261 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0256 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02572 | hp2 | a0002 | c0023 | t0031 | g0235 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02602 | hp1 | a0001 | c0012 | t0001 | g0005 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02615 | hp1 | a0003 | c0007 | t0028 | g0234 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02615 | hp2 | a0001 | c0012 | t0008 | g0168 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02622 | hp1 | a0002 | c0004 | t0030 | g0244 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02630 | hp1 | a0002 | c0004 | t0020 | g0026 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02630 | hp2 | a0002 | c0003 | t0003 | g0043 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02683 | hp2 | a0004 | c0018 | t0008 | g0155 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0033 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02717 | hp1 | a0003 | c0006 | t0007 | g0251 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02717 | hp2 | a0003 | c0006 | t0007 | g0174 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02723 | hp1 | a0003 | c0007 | t0006 | g0239 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0220 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0191 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02809 | hp1 | a0004 | c0024 | t0008 | g0139 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0058 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02818 | hp1 | a0002 | c0003 | t0003 | g0042 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02818 | hp2 | a0008 | c0020 | t0002 | g0080 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02895 | hp1 | a0002 | c0005 | t0013 | g0066 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02895 | hp2 | a0003 | c0007 | t0006 | g0262 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02896 | hp1 | a0002 | c0005 | t0019 | g0241 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02896 | hp2 | a0004 | c0014 | t0002 | g0062 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02897 | hp1 | a0003 | c0007 | t0006 | g0169 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02897 | hp2 | a0004 | c0014 | t0002 | g0063 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02922 | hp1 | a0005 | c0015 | t0017 | g0067 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02922 | hp2 | a0004 | c0014 | t0002 | g0260 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02965 | hp1 | a0003 | c0007 | t0006 | g0255 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02965 | hp2 | a0002 | c0010 | t0009 | g0068 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02970 | hp1 | a0003 | c0006 | t0007 | g0170 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0149 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02976 | hp1 | a0003 | c0006 | t0007 | g0245 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02976 | hp2 | a0004 | c0011 | t0008 | g0258 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03041 | hp1 | a0003 | c0007 | t0006 | g0236 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03041 | hp2 | a0002 | c0003 | t0003 | g0054 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03098 | hp1 | a0002 | c0005 | t0019 | g0240 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03098 | hp2 | a0003 | c0006 | t0007 | g0165 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03130 | hp1 | a0002 | c0004 | t0003 | g0153 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03139 | hp1 | a0003 | c0017 | t0006 | g0199 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03139 | hp2 | a0002 | c0003 | t0026 | g0167 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03195 | hp1 | a0001 | c0021 | t0005 | g0044 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03195 | hp2 | a0003 | c0007 | t0006 | g0238 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03225 | hp1 | a0002 | c0004 | t0033 | g0151 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03225 | hp2 | a0002 | c0003 | t0003 | g0047 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03453 | hp1 | a0002 | c0003 | t0003 | g0001 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03453 | hp2 | a0003 | c0006 | t0007 | g0173 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03486 | hp1 | a0002 | c0009 | t0011 | g0246 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03486 | hp2 | a0002 | c0003 | t0016 | g0253 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03490 | hp1 | a0001 | c0001 | t0024 | g0123 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03491 | hp2 | a0001 | c0008 | t0005 | g0018 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03516 | hp1 | a0003 | c0016 | t0027 | g0004 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03516 | hp2 | a0001 | c0001 | t0023 | g0134 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03540 | hp1 | a0002 | c0003 | t0003 | g0028 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03540 | hp2 | a0002 | c0026 | t0016 | g0254 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0064 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03579 | hp2 | a0001 | c0012 | t0002 | g0041 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03654 | hp1 | a0001 | c0002 | t0015 | g0009 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03669 | hp1 | a0002 | c0004 | t0003 | g0060 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0050 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03927 | hp2 | a0002 | c0003 | t0003 | g0051 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04204 | hp1 | a0001 | c0002 | t0015 | g0006 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0175 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18522 | hp1 | a0003 | c0016 | t0007 | g0003 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18522 | hp2 | a0002 | c0004 | t0020 | g0052 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18747 | hp1 | a0002 | c0004 | t0012 | g0219 | EAS | CHB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18906 | hp1 | a0002 | c0005 | t0018 | g0224 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18906 | hp2 | a0002 | c0004 | t0003 | g0154 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18943 | hp1 | a0001 | c0008 | t0005 | g0036 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18963 | hp2 | a0001 | c0008 | t0005 | g0015 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18964 | hp1 | a0001 | c0008 | t0005 | g0013 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18965 | hp2 | a0001 | c0013 | t0005 | g0269 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18966 | hp1 | a0001 | c0008 | t0005 | g0014 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18968 | hp2 | a0001 | c0022 | t0001 | g0102 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18980 | hp2 | a0001 | c0013 | t0005 | g0128 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18981 | hp2 | a0001 | c0002 | t0021 | g0158 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18983 | hp2 | a0009 | c0019 | t0022 | g0100 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18985 | hp2 | a0001 | c0013 | t0005 | g0265 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19010 | hp1 | a0001 | c0002 | t0014 | g0268 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19012 | hp1 | a0001 | c0002 | t0014 | g0266 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19043 | hp1 | a0002 | c0009 | t0011 | g0248 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19043 | hp2 | a0004 | c0011 | t0008 | g0259 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19055 | hp1 | a0001 | c0001 | t0034 | g0156 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19056 | hp2 | a0001 | c0008 | t0005 | g0012 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19070 | hp1 | a0002 | c0005 | t0003 | g0223 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19080 | hp2 | a0001 | c0002 | t0014 | g0267 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19089 | hp2 | a0001 | c0008 | t0025 | g0019 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19240 | hp1 | a0005 | c0015 | t0017 | g0020 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0164 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20129 | hp1 | a0002 | c0004 | t0032 | g0056 | AFR | ASW | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ASW | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0040 | EUR | TSI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0206 | SAS | GIH | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0213 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02109 | hp1 | a0003 | c0006 | t0007 | g0172 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02109 | hp2 | a0002 | c0004 | t0003 | g0242 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02486 | hp1 | a0007 | c0025 | t0003 | g0024 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02559 | hp1 | a0003 | c0017 | t0006 | g0152 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02559 | hp2 | a0002 | c0005 | t0018 | g0045 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG06807 | hp1 | a0003 | c0006 | t0007 | g0171 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG06807 | hp2 | a0002 | c0003 | t0003 | g0250 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA21309 | hp1 | a0003 | c0007 | t0006 | g0237 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA21309 | hp2 | a0002 | c0003 | t0003 | g0252 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0150 | REF | REF | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0075 | REF | REF | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54870280 | G | A | 1 | a0009 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.34G>A | p.Asp12Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 150/6244 | 34/3036 | 12/1011 | chr6 | 54870280 | |||
| chr6:54870665 | G | A | 1 | a0008 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.419G>A | p.Arg140Gln | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 535/6244 | 419/3036 | 140/1011 | chr6 | 54870665 | |||
| chr6:54927521 | G | A | 1 | a0005 | 2 | HG02922.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.623G>A | p.Arg208Gln | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/5 | 739/6244 | 623/3036 | 208/1011 | chr6 | 54927521 | |||
| chr6:54927622 | G | A | 1 | a0006 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.724G>A | p.Gly242Ser | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/5 | 840/6244 | 724/3036 | 242/1011 | chr6 | 54927622 | |||
| chr6:54940200 | A | G | 1 | a0004 | 10 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
missense_variant | MODERATE | c.1229A>G | p.Asn410Ser | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1345/6244 | 1229/3036 | 410/1011 | chr6 | 54940200 | |||
| chr6:54940276 | C | G | 2 | a0003 a0005 |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
missense_variant | MODERATE | c.1305C>G | p.Ser435Arg | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1421/6244 | 1305/3036 | 435/1011 | chr6 | 54940276 | |||
| chr6:54940839 | C | G | 1 | a0007 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1868C>G | p.Ala623Gly | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1984/6244 | 1868/3036 | 623/1011 | chr6 | 54940839 | |||
| chr6:54940890 | A | C | 4 | a0002 a0003 a0005 others(1): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
missense_variant | MODERATE | c.1919A>C | p.Lys640Thr | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2035/6244 | 1919/3036 | 640/1011 | chr6 | 54940890 | |||
| chr6:54941691 | C | A | 4 | a0002 a0003 a0005 others(1): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
missense_variant | MODERATE | c.2720C>A | p.Thr907Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2836/6244 | 2720/3036 | 907/1011 | chr6 | 54941691 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54870324 | A | G | 8 | a0001c0002 a0001c0013 a0002c0005 others(5): Show |
96 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
synonymous_variant | LOW | c.78A>G | p.Glu26Glu | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 194/6244 | 78/3036 | 26/1011 | chr6 | 54870324 | |||
| chr6:54870546 | A | G | 4 | a0001c0012 a0002c0003 a0002c0026 others(1): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
synonymous_variant | LOW | c.300A>G | p.Glu100Glu | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 416/6244 | 300/3036 | 100/1011 | chr6 | 54870546 | |||
| chr6:54870585 | C | T | 2 | a0002c0009 a0003c0006 |
15 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
synonymous_variant | LOW | c.339C>T | p.Pro113Pro | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 455/6244 | 339/3036 | 113/1011 | chr6 | 54870585 | |||
| chr6:54926424 | C | T | 1 | a0002c0026 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.498C>T | p.Ile166Ile | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/5 | 614/6244 | 498/3036 | 166/1011 | chr6 | 54926424 | |||
| chr6:54940000 | T | C | 3 | a0001c0008 a0001c0013 a0001c0021 |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
synonymous_variant | LOW | c.1029T>C | p.Tyr343Tyr | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1145/6244 | 1029/3036 | 343/1011 | chr6 | 54940000 | |||
| chr6:54940081 | C | T | 3 | a0004c0011 a0004c0018 a0004c0024 |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
synonymous_variant | LOW | c.1110C>T | p.Asn370Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1226/6244 | 1110/3036 | 370/1011 | chr6 | 54940081 | |||
| chr6:54940144 | G | A | 2 | a0004c0011 a0004c0024 |
5 | HG02145.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1173G>A | p.Gly391Gly | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1289/6244 | 1173/3036 | 391/1011 | chr6 | 54940144 | |||
| chr6:54940468 | C | T | 1 | a0002c0023 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1497C>T | p.Ser499Ser | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1613/6244 | 1497/3036 | 499/1011 | chr6 | 54940468 | |||
| chr6:54941041 | G | A | 1 | a0001c0022 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.2070G>A | p.Arg690Arg | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2186/6244 | 2070/3036 | 690/1011 | chr6 | 54941041 | |||
| chr6:54941581 | A | G | 2 | a0002c0010 a0002c0028 |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
synonymous_variant | LOW | c.2610A>G | p.Pro870Pro | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2726/6244 | 2610/3036 | 870/1011 | chr6 | 54941581 | |||
| chr6:54941788 | G | A | 1 | a0001c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2817G>A | p.Pro939Pro | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2933/6244 | 2817/3036 | 939/1011 | chr6 | 54941788 | |||
| chr6:54941827 | C | T | 2 | a0003c0007 a0003c0017 |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
synonymous_variant | LOW | c.2856C>T | p.Asn952Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2972/6244 | 2856/3036 | 952/1011 | chr6 | 54941827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54942208 | T | G | 47 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(44): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*201T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 201 | chr6 | 54942208 | ||||||
| chr6:54942367 | C | T | 1 | a0001c0001t0035 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 360 | chr6 | 54942367 | ||||||
| chr6:54942565 | A | AT | 2 | a0001c0001t0004 a0001c0001t0034 |
13 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*567dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 568 | INFO_REALIGN_3_PRIME | chr6 | 54942565 | |||||
| chr6:54942644 | A | C | 1 | a0002c0004t0033 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*637A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 637 | chr6 | 54942644 | ||||||
| chr6:54942715 | A | AGGCTGCT others(128): Show |
1 | a0002c0009t0011 | 5 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(129): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(129): Show |
1 | a0002c0009t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(130): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(142): Show |
1 | a0002c0004t0030 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(143): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(150): Show |
1 | a0002c0023t0031 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(151): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(154): Show |
1 | a0002c0005t0013 | 3 | HG01884.hp2 HG01891.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(155): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(155): Show |
1 | a0002c0005t0018 | 2 | HG02559.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(156): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(160): Show |
1 | a0002c0005t0019 | 2 | HG02896.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(161): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(164): Show |
1 | a0002c0004t0032 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(165): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942715 | A | AGGCTGCT others(167): Show |
1 | a0002c0004t0020 | 2 | HG02630.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(168): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | |||||
| chr6:54942783 | C | T | 7 | a0003c0006t0007 a0003c0007t0006 a0003c0007t0028 others(4): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*776C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 776 | chr6 | 54942783 | ||||||
| chr6:54942824 | T | A | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(8): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*817T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 817 | chr6 | 54942824 | ||||||
| chr6:54942856 | A | T | 1 | a0001c0001t0024 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 849 | chr6 | 54942856 | ||||||
| chr6:54942890 | C | T | 9 | a0002c0004t0020 a0002c0004t0030 a0002c0004t0032 others(6): Show |
18 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*883C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 883 | chr6 | 54942890 | ||||||
| chr6:54942904 | C | CT | 6 | a0002c0003t0003 a0002c0003t0026 a0002c0004t0003 others(3): Show |
34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*908dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 909 | INFO_REALIGN_3_PRIME | chr6 | 54942904 | |||||
| chr6:54942944 | C | T | 1 | a0003c0007t0028 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 937 | chr6 | 54942944 | ||||||
| chr6:54942948 | G | C | 1 | a0009c0019t0022 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*941G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 941 | chr6 | 54942948 | ||||||
| chr6:54943153 | G | A | 1 | a0001c0002t0015 | 2 | HG03654.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1146G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1146 | chr6 | 54943153 | ||||||
| chr6:54943190 | C | A | 1 | a0001c0001t0010 | 5 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1183C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1183 | chr6 | 54943190 | ||||||
| chr6:54943231 | T | C | 47 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(44): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1224T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1224 | chr6 | 54943231 | ||||||
| chr6:54943232 | G | A | 1 | a0005c0015t0017 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1225G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1225 | chr6 | 54943232 | ||||||
| chr6:54943244 | T | C | 1 | a0001c0002t0021 | 2 | HG02165.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1237T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1237 | chr6 | 54943244 | ||||||
| chr6:54943268 | G | T | 1 | a0001c0001t0034 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1261 | chr6 | 54943268 | ||||||
| chr6:54943540 | T | C | 1 | a0001c0002t0014 | 3 | NA19010.hp1 NA19012.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1533T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1533 | chr6 | 54943540 | ||||||
| chr6:54943544 | G | A | 27 | a0002c0003t0003 a0002c0003t0016 a0002c0003t0026 others(24): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1537G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1537 | chr6 | 54943544 | ||||||
| chr6:54943742 | A | G | 27 | a0002c0003t0003 a0002c0003t0016 a0002c0003t0026 others(24): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1735A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1735 | chr6 | 54943742 | ||||||
| chr6:54943763 | A | G | 1 | a0003c0016t0027 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1756 | chr6 | 54943763 | ||||||
| chr6:54943870 | C | G | 3 | a0003c0006t0007 a0003c0016t0007 a0003c0016t0027 |
11 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1863C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1863 | chr6 | 54943870 | ||||||
| chr6:54943918 | T | C | 1 | a0001c0008t0025 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1911T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1911 | chr6 | 54943918 | ||||||
| chr6:54944053 | G | A | 4 | a0001c0008t0005 a0001c0008t0025 a0001c0013t0005 others(1): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2046G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2046 | chr6 | 54944053 | ||||||
| chr6:54944090 | C | T | 1 | a0002c0003t0026 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2083C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2083 | chr6 | 54944090 | ||||||
| chr6:54944101 | A | G | 3 | a0003c0007t0006 a0003c0007t0028 a0003c0017t0006 |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2094A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2094 | chr6 | 54944101 | ||||||
| chr6:54944163 | T | A | 2 | a0002c0010t0009 a0002c0028t0009 |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2156T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2156 | chr6 | 54944163 | ||||||
| chr6:54944166 | G | T | 4 | a0003c0006t0007 a0003c0016t0007 a0003c0016t0027 others(1): Show |
13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2159G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2159 | chr6 | 54944166 | ||||||
| chr6:54944304 | C | A | 20 | a0002c0003t0003 a0002c0003t0016 a0002c0003t0026 others(17): Show |
61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2297C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2297 | chr6 | 54944304 | ||||||
| chr6:54944486 | A | G | 1 | a0002c0004t0012 | 4 | HG00438.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2479A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2479 | chr6 | 54944486 | ||||||
| chr6:54944656 | C | T | 2 | a0002c0010t0009 a0002c0028t0009 |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2649C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2649 | chr6 | 54944656 | ||||||
| chr6:54944695 | C | T | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(17): Show |
113 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2688C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2688 | chr6 | 54944695 | ||||||
| chr6:54944789 | C | T | 6 | a0002c0003t0003 a0002c0003t0026 a0002c0004t0003 others(3): Show |
34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2782 | chr6 | 54944789 | ||||||
| chr6:54944791 | T | A | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(17): Show |
113 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2784T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2784 | chr6 | 54944791 | ||||||
| chr6:54944966 | C | T | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2959C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2959 | chr6 | 54944966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54846875 | C | T | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+49C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846875 | |||||||
| chr6:54846906 | A | G | 107 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(104): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-61+80A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846906 | |||||||
| chr6:54846908 | T | TG | 69 | a0001c0001t0001g0182 a0001c0001t0001g0192 a0001c0001t0001g0193 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-61+89dupG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54846908 | ||||||
| chr6:54846908 | T | TGGG | 21 | a0001c0002t0002g0256 a0002c0003t0003g0250 a0002c0003t0003g0252 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-61+87_-61+89dupGG others(1): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54846908 | ||||||
| chr6:54846909 | G | C | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+83G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846909 | |||||||
| chr6:54846916 | C | G | 107 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(104): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-61+90C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846916 | |||||||
| chr6:54846988 | C | A | 6 | a0001c0001t0001g0010 a0001c0002t0015g0006 a0001c0002t0015g0009 others(3): Show |
6 | HG00280.hp1 HG00642.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61+162C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846988 | |||||||
| chr6:54847040 | C | T | 5 | a0003c0006t0007g0170 a0003c0006t0007g0171 a0003c0006t0007g0172 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61+214C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847040 | |||||||
| chr6:54847061 | G | A | 16 | a0001c0001t0001g0011 a0001c0002t0002g0264 a0001c0002t0002g0270 others(13): Show |
16 | HG00544.hp1 HG02015.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-61+235G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847061 | |||||||
| chr6:54847100 | C | T | 9 | a0001c0001t0001g0011 a0001c0008t0005g0012 a0001c0008t0005g0013 others(6): Show |
9 | HG00544.hp1 HG02258.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61+274C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847100 | |||||||
| chr6:54847193 | C | T | 13 | a0001c0002t0002g0256 a0001c0012t0008g0168 a0002c0003t0016g0253 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-61+367C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847193 | |||||||
| chr6:54847214 | GAGACCGC others(22): Show |
G | 9 | a0002c0004t0003g0242 a0002c0005t0019g0240 a0002c0005t0019g0241 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-61+391_-61+419del others(29): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54847214 | ||||||
| chr6:54847342 | G | T | 1 | a0004c0018t0008g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-61+516G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847342 | |||||||
| chr6:54847391 | G | T | 3 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0003c0017t0006g0152 |
3 | HG02559.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-61+565G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847391 | |||||||
| chr6:54847429 | CTG | C | 108 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(105): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-61+607_-61+608del others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54847429 | ||||||
| chr6:54847527 | C | G | 2 | a0002c0003t0003g0252 a0002c0003t0026g0167 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-61+701C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847527 | |||||||
| chr6:54847623 | TG | T | 60 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(57): Show |
61 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-61+798delG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847623 | |||||||
| chr6:54847624 | G | C | 1 | a0005c0015t0017g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-61+798G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847624 | |||||||
| chr6:54847626 | G | A | 61 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(58): Show |
62 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.-61+800G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847626 | |||||||
| chr6:54847731 | A | G | 6 | a0001c0001t0001g0010 a0001c0002t0015g0006 a0001c0002t0015g0009 others(3): Show |
6 | HG00280.hp1 HG00642.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61+905A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847731 | |||||||
| chr6:54847760 | G | A | 107 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(104): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-61+934G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847760 | |||||||
| chr6:54847873 | A | G | 1 | a0002c0004t0003g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-61+1047A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847873 | |||||||
| chr6:54848092 | T | G | 39 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0035g0022 others(36): Show |
40 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-61+1266T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848092 | |||||||
| chr6:54848103 | A | AG | 3 | a0001c0002t0002g0177 a0001c0012t0001g0005 a0002c0004t0012g0176 |
3 | HG00438.hp2 HG01109.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-61+1278dupG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54848103 | ||||||
| chr6:54848105 | T | G | 183 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-61+1279T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848105 | |||||||
| chr6:54848106 | G | C | 39 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0035g0022 others(36): Show |
40 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-61+1280G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848106 | |||||||
| chr6:54848111 | T | G | 1 | a0001c0002t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-61+1285T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848111 | |||||||
| chr6:54848111 | T | TG | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0010g0058 others(6): Show |
9 | HG01243.hp1 HG02027.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61+1290dupG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54848111 | ||||||
| chr6:54848172 | T | G | 1 | a0006c0027t0002g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-61+1346T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848172 | |||||||
| chr6:54848225 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-61+1399T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848225 | |||||||
| chr6:54848259 | C | T | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+1433C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848259 | |||||||
| chr6:54848290 | G | T | 10 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0255 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-61+1464G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848290 | |||||||
| chr6:54848699 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-61+1873A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848699 | |||||||
| chr6:54848902 | T | A | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+2076T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848902 | |||||||
| chr6:54849030 | A | G | 61 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(58): Show |
62 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.-61+2204A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849030 | |||||||
| chr6:54849104 | C | T | 75 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(72): Show |
76 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-61+2278C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849104 | |||||||
| chr6:54849253 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-61+2427C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849253 | |||||||
| chr6:54849254 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-61+2428A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849254 | |||||||
| chr6:54849463 | C | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(47): Show |
51 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.-61+2637C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849463 | |||||||
| chr6:54849464 | T | C | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-61+2638T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849464 | |||||||
| chr6:54849573 | G | A | 2 | a0004c0018t0008g0059 a0004c0018t0008g0155 |
2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-61+2747G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849573 | |||||||
| chr6:54849632 | T | C | 8 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(5): Show |
8 | HG00544.hp1 HG02258.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+2806T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849632 | |||||||
| chr6:54849739 | T | TAAGAGTG others(317): Show |
2 | a0002c0003t0003g0054 a0002c0003t0003g0055 |
2 | HG01069.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(326): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849739 | T | TAAGAGTG others(318): Show |
29 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(26): Show |
30 | HG00735.hp2 HG01167.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(327): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849739 | T | TAAGAGTG others(319): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0002c0003t0003g0021 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(328): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849739 | T | TAAGAGTG others(320): Show |
1 | a0001c0001t0035g0022 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-61+2927_-61+2928i others(329): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849739 | T | TAAGAGTG others(315): Show |
2 | a0002c0010t0009g0068 a0002c0010t0009g0069 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(324): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849739 | T | TAAGAGTG others(318): Show |
1 | a0002c0004t0032g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-61+2927_-61+2928i others(327): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849739 | T | TAAGAGTG others(320): Show |
1 | a0001c0002t0002g0057 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-61+2927_-61+2928i others(329): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | ||||||
| chr6:54849837 | T | G | 115 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(112): Show |
115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-61+3011T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849837 | |||||||
| chr6:54849962 | C | G | 41 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0035g0022 others(38): Show |
42 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-61+3136C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849962 | |||||||
| chr6:54849975 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-61+3149C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849975 | |||||||
| chr6:54850249 | T | A | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+3423T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850249 | |||||||
| chr6:54850249 | T | C | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+3423T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850249 | |||||||
| chr6:54850320 | A | C | 1 | a0002c0003t0003g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-61+3494A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850320 | |||||||
| chr6:54850328 | A | C | 119 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(116): Show |
119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-61+3502A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850328 | |||||||
| chr6:54850389 | C | T | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+3563C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850389 | |||||||
| chr6:54850402 | T | C | 13 | a0001c0002t0002g0256 a0001c0012t0008g0168 a0002c0003t0016g0253 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-61+3576T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850402 | |||||||
| chr6:54850409 | G | T | 1 | a0002c0004t0032g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-61+3583G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850409 | |||||||
| chr6:54850476 | G | T | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+3650G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850476 | |||||||
| chr6:54850879 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-61+4053C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850879 | |||||||
| chr6:54850879 | C | T | 1 | a0002c0004t0020g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-61+4053C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850879 | |||||||
| chr6:54850946 | A | C | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+4120A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850946 | |||||||
| chr6:54850959 | A | G | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-61+4133A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850959 | |||||||
| chr6:54850972 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-61+4146C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850972 | |||||||
| chr6:54850974 | C | T | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-61+4148C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850974 | |||||||
| chr6:54850989 | G | T | 1 | a0001c0001t0010g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-61+4163G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850989 | |||||||
| chr6:54851016 | CA | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(141): Show |
146 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-61+4212delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851016 | ||||||
| chr6:54851016 | CAA | C | 90 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(87): Show |
90 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-61+4211_-61+4212d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851016 | ||||||
| chr6:54851016 | CAAA | C | 19 | a0001c0002t0002g0256 a0002c0003t0003g0164 a0002c0003t0016g0253 others(16): Show |
19 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-61+4210_-61+4212d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851016 | ||||||
| chr6:54851038 | A | C | 103 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(100): Show |
103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-61+4212A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851038 | |||||||
| chr6:54851146 | A | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-61+4320A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851146 | |||||||
| chr6:54851288 | C | A | 2 | a0001c0002t0002g0183 a0002c0028t0009g0188 |
2 | HG00323.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-61+4462C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851288 | |||||||
| chr6:54851386 | C | T | 186 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(183): Show |
187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-61+4560C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851386 | |||||||
| chr6:54851493 | G | A | 2 | a0002c0010t0009g0068 a0002c0010t0009g0069 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-61+4667G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851493 | |||||||
| chr6:54851647 | G | GT | 93 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0143 others(90): Show |
93 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-61+4839dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851647 | ||||||
| chr6:54851647 | G | GTT | 38 | a0001c0001t0001g0161 a0001c0002t0001g0157 a0001c0002t0001g0230 others(35): Show |
38 | HG00741.hp2 HG01109.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.-61+4838_-61+4839d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851647 | ||||||
| chr6:54851647 | G | GTTT | 6 | a0001c0001t0010g0149 a0001c0002t0002g0270 a0001c0002t0014g0268 others(3): Show |
6 | HG02015.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61+4837_-61+4839d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851647 | ||||||
| chr6:54851710 | A | G | 184 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-61+4884A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851710 | |||||||
| chr6:54851714 | C | G | 1 | a0001c0001t0004g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-61+4888C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851714 | |||||||
| chr6:54851737 | T | C | 1 | a0002c0005t0013g0066 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-61+4911T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851737 | |||||||
| chr6:54851738 | C | T | 1 | a0002c0005t0013g0066 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-61+4912C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851738 | |||||||
| chr6:54851748 | T | C | 186 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(183): Show |
187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-61+4922T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851748 | |||||||
| chr6:54851796 | C | T | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+4970C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851796 | |||||||
| chr6:54851802 | T | C | 8 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(5): Show |
8 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+4976T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851802 | |||||||
| chr6:54851809 | G | A | 57 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(54): Show |
58 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-61+4983G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851809 | |||||||
| chr6:54851839 | G | A | 8 | a0001c0002t0002g0177 a0001c0002t0002g0183 a0001c0002t0002g0184 others(5): Show |
8 | HG00323.hp1 HG01109.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+5013G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851839 | |||||||
| chr6:54851875 | T | C | 112 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(109): Show |
112 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-61+5049T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851875 | |||||||
| chr6:54851886 | A | G | 1 | a0001c0002t0002g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-61+5060A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851886 | |||||||
| chr6:54851927 | G | A | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-61+5101G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851927 | |||||||
| chr6:54851942 | C | T | 2 | a0001c0012t0008g0168 a0002c0026t0016g0254 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-61+5116C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851942 | |||||||
| chr6:54851945 | CCTAATTT others(134): Show |
C | 8 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(5): Show |
8 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+5121_-61+5261d others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851945 | ||||||
| chr6:54851975 | G | A | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+5149G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851975 | |||||||
| chr6:54852015 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-61+5189T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852015 | |||||||
| chr6:54852073 | G | A | 8 | a0001c0002t0002g0046 a0001c0021t0005g0044 a0002c0003t0003g0021 others(5): Show |
8 | HG01069.hp2 HG01243.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+5247G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852073 | |||||||
| chr6:54852288 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0035g0022 others(20): Show |
24 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.-61+5462G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852288 | |||||||
| chr6:54852333 | A | G | 112 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(109): Show |
112 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-61+5507A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852333 | |||||||
| chr6:54852336 | A | G | 1 | a0004c0024t0008g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-61+5510A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852336 | |||||||
| chr6:54852409 | T | G | 64 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+5583T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852409 | |||||||
| chr6:54852431 | C | T | 65 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(62): Show |
66 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-61+5605C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852431 | |||||||
| chr6:54852586 | G | A | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+5760G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852586 | |||||||
| chr6:54852691 | T | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | NA18943.hp2 NA18950.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-61+5865T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852691 | |||||||
| chr6:54852754 | C | G | 14 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(11): Show |
14 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-61+5928C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852754 | |||||||
| chr6:54852899 | T | A | 57 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(54): Show |
58 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-61+6073T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852899 | |||||||
| chr6:54852938 | A | AT | 166 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(163): Show |
167 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-61+6121dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54852938 | ||||||
| chr6:54852938 | A | ATT | 20 | a0001c0001t0010g0149 a0001c0012t0008g0168 a0002c0004t0003g0060 others(17): Show |
20 | HG01175.hp2 HG02109.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.-61+6120_-61+6121d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54852938 | ||||||
| chr6:54852969 | ATTG | A | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+6149_-61+6151d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54852969 | ||||||
| chr6:54852974 | T | C | 113 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(110): Show |
113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-61+6148T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852974 | |||||||
| chr6:54852991 | C | T | 1 | a0001c0001t0035g0022 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-61+6165C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852991 | |||||||
| chr6:54853101 | C | A | 1 | a0001c0012t0001g0005 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-61+6275C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853101 | |||||||
| chr6:54853118 | C | T | 29 | a0001c0002t0002g0256 a0002c0003t0003g0164 a0002c0003t0003g0250 others(26): Show |
29 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.-61+6292C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853118 | |||||||
| chr6:54853195 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(264): Show |
269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-61+6369A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853195 | |||||||
| chr6:54853338 | C | A | 177 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(174): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-61+6512C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853338 | |||||||
| chr6:54853380 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-61+6554G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853380 | |||||||
| chr6:54853508 | A | C | 1 | a0001c0002t0002g0035 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-61+6682A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853508 | |||||||
| chr6:54853771 | G | T | 2 | a0003c0007t0006g0169 a0003c0007t0006g0262 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-61+6945G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853771 | |||||||
| chr6:54853795 | T | C | 64 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+6969T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853795 | |||||||
| chr6:54853805 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-61+6979A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853805 | |||||||
| chr6:54853891 | A | T | 177 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0025 others(174): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-61+7065A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853891 | |||||||
| chr6:54853894 | A | G | 3 | a0002c0003t0003g0164 a0003c0006t0007g0165 a0003c0006t0007g0166 |
3 | HG02280.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-61+7068A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853894 | |||||||
| chr6:54854006 | G | T | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+7180G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854006 | |||||||
| chr6:54854027 | A | T | 11 | a0001c0002t0002g0256 a0002c0003t0016g0253 a0003c0007t0006g0169 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-61+7201A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854027 | |||||||
| chr6:54854047 | G | A | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+7221G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854047 | |||||||
| chr6:54854238 | A | C | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-61+7412A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854238 | |||||||
| chr6:54854336 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-61+7510G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854336 | |||||||
| chr6:54854573 | T | C | 1 | a0001c0002t0002g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-61+7747T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854573 | |||||||
| chr6:54854687 | T | C | 64 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+7861T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854687 | |||||||
| chr6:54854872 | A | G | 23 | a0001c0002t0002g0256 a0002c0003t0016g0253 a0002c0004t0003g0153 others(20): Show |
23 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-61+8046A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854872 | |||||||
| chr6:54854893 | G | A | 64 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+8067G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854893 | |||||||
| chr6:54855001 | T | C | 1 | a0001c0002t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-61+8175T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855001 | |||||||
| chr6:54855122 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-61+8296G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855122 | |||||||
| chr6:54855194 | T | C | 2 | a0002c0010t0009g0068 a0002c0010t0009g0069 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-61+8368T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855194 | |||||||
| chr6:54855281 | G | C | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+8455G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855281 | |||||||
| chr6:54855332 | A | G | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+8506A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855332 | |||||||
| chr6:54855477 | G | C | 83 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(80): Show |
83 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-61+8651G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855477 | |||||||
| chr6:54855481 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-61+8655A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855481 | |||||||
| chr6:54855645 | G | A | 64 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+8819G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855645 | |||||||
| chr6:54855687 | C | T | 64 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0192 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+8861C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855687 | |||||||
| chr6:54855776 | C | T | 2 | a0003c0006t0007g0165 a0003c0006t0007g0166 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-61+8950C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855776 | |||||||
| chr6:54855880 | A | C | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+9054A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855880 | |||||||
| chr6:54856236 | C | T | 1 | a0001c0002t0002g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-61+9410C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856236 | |||||||
| chr6:54856238 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-61+9412A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856238 | |||||||
| chr6:54856286 | C | T | 33 | a0001c0012t0008g0168 a0002c0003t0003g0164 a0002c0003t0003g0250 others(30): Show |
33 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.-61+9460C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856286 | |||||||
| chr6:54856461 | T | A | 6 | a0001c0001t0001g0010 a0001c0002t0015g0006 a0001c0002t0015g0009 others(3): Show |
6 | HG00280.hp1 HG00642.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61+9635T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856461 | |||||||
| chr6:54856579 | ATTTC | A | 17 | a0002c0003t0003g0164 a0002c0003t0003g0250 a0002c0004t0030g0244 others(14): Show |
17 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-61+9757_-61+9760d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54856579 | ||||||
| chr6:54856683 | G | A | 12 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(9): Show |
12 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-61+9857G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856683 | |||||||
| chr6:54856819 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0182 others(107): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-61+9993G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856819 | |||||||
| chr6:54856937 | A | C | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-61+10111A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856937 | |||||||
| chr6:54857022 | C | T | 24 | a0001c0001t0001g0010 a0001c0002t0015g0006 a0001c0002t0015g0009 others(21): Show |
24 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-61+10196C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857022 | |||||||
| chr6:54857141 | G | A | 10 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(7): Show |
10 | HG00544.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-61+10315G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857141 | |||||||
| chr6:54857164 | A | C | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-61+10338A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857164 | |||||||
| chr6:54857215 | A | G | 77 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0010g0058 others(74): Show |
78 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.-61+10389A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857215 | |||||||
| chr6:54857309 | G | A | 1 | a0001c0002t0002g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-61+10483G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857309 | |||||||
| chr6:54857394 | G | C | 1 | a0001c0002t0002g0029 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-61+10568G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857394 | |||||||
| chr6:54857408 | A | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+10582A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857408 | |||||||
| chr6:54857527 | C | T | 10 | a0002c0003t0016g0253 a0003c0007t0006g0169 a0003c0007t0006g0255 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-61+10701C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857527 | |||||||
| chr6:54857726 | T | C | 21 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(18): Show |
21 | HG02015.hp1 HG02109.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.-61+10900T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857726 | |||||||
| chr6:54857773 | A | G | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+10947A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857773 | |||||||
| chr6:54857813 | C | T | 3 | a0001c0002t0002g0183 a0001c0002t0002g0184 a0002c0028t0009g0188 |
3 | HG00323.hp1 HG02293.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-61+10987C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857813 | |||||||
| chr6:54857838 | T | C | 1 | a0001c0001t0010g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-61+11012T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857838 | |||||||
| chr6:54857959 | G | A | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-61+11133G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857959 | |||||||
| chr6:54858036 | A | C | 1 | a0001c0002t0015g0009 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-61+11210A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858036 | |||||||
| chr6:54858261 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | NA18943.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-61+11435A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858261 | |||||||
| chr6:54858345 | A | G | 1 | a0001c0001t0023g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-61+11519A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858345 | |||||||
| chr6:54858550 | T | C | 2 | a0002c0004t0032g0056 a0002c0005t0013g0066 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-60-11637T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858550 | |||||||
| chr6:54858556 | TA | T | 14 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(11): Show |
14 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-60-11628delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54858556 | ||||||
| chr6:54858577 | C | T | 1 | a0002c0005t0003g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-60-11610C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858577 | |||||||
| chr6:54858809 | A | G | 7 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(4): Show |
7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-11378A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858809 | |||||||
| chr6:54859012 | G | A | 177 | a0001c0001t0001g0083 a0001c0001t0001g0161 a0001c0001t0001g0182 others(174): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-60-11175G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859012 | |||||||
| chr6:54859047 | G | A | 1 | a0001c0001t0010g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-60-11140G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859047 | |||||||
| chr6:54859047 | G | C | 176 | a0001c0001t0001g0083 a0001c0001t0001g0161 a0001c0001t0001g0182 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-60-11140G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859047 | |||||||
| chr6:54859060 | C | T | 1 | a0002c0005t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-60-11127C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859060 | |||||||
| chr6:54859093 | C | G | 1 | a0002c0003t0003g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-60-11094C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859093 | |||||||
| chr6:54859098 | T | C | 16 | a0002c0004t0003g0060 a0002c0010t0009g0007 a0002c0010t0009g0008 others(13): Show |
16 | HG00280.hp1 HG00642.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-60-11089T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859098 | |||||||
| chr6:54859154 | G | A | 18 | a0002c0003t0003g0164 a0002c0003t0003g0250 a0002c0004t0030g0244 others(15): Show |
18 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-60-11033G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859154 | |||||||
| chr6:54859176 | C | T | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-60-11011C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859176 | |||||||
| chr6:54859189 | G | A | 14 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(11): Show |
14 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-60-10998G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859189 | |||||||
| chr6:54859282 | C | T | 12 | a0002c0004t0003g0060 a0003c0007t0006g0169 a0003c0007t0006g0255 others(9): Show |
12 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-10905C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859282 | |||||||
| chr6:54859376 | T | C | 4 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-60-10811T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859376 | |||||||
| chr6:54859481 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-60-10706G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859481 | |||||||
| chr6:54859607 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0025 others(183): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-60-10580A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859607 | |||||||
| chr6:54859743 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01258.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-60-10444G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859743 | |||||||
| chr6:54860043 | T | TTG | 5 | a0001c0001t0010g0064 a0001c0001t0010g0065 a0001c0001t0010g0200 others(2): Show |
5 | HG00280.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-10118_-60-1011 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | ||||||
| chr6:54860043 | TTG | T | 88 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(85): Show |
88 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-60-10118_-60-1011 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | ||||||
| chr6:54860043 | TTGTG | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
136 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-60-10120_-60-1011 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | ||||||
| chr6:54860043 | TTGTGTG | T | 12 | a0003c0007t0006g0169 a0003c0007t0006g0239 a0003c0007t0006g0255 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-10122_-60-1011 others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | ||||||
| chr6:54860075 | C | A | 10 | a0003c0007t0006g0169 a0003c0007t0006g0239 a0003c0007t0006g0255 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-60-10112C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860075 | |||||||
| chr6:54860446 | G | A | 13 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(10): Show |
13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-60-9741G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860446 | |||||||
| chr6:54860872 | C | T | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-60-9315C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860872 | |||||||
| chr6:54860882 | T | C | 10 | a0003c0007t0006g0169 a0003c0007t0006g0239 a0003c0007t0006g0255 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-60-9305T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860882 | |||||||
| chr6:54860883 | G | C | 1 | a0003c0007t0006g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-60-9304G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860883 | |||||||
| chr6:54860916 | C | T | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-9271C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860916 | |||||||
| chr6:54861131 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-60-9056A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861131 | |||||||
| chr6:54861380 | C | G | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-8807C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861380 | |||||||
| chr6:54861503 | GC | G | 3 | a0002c0005t0013g0066 a0004c0014t0002g0062 a0004c0014t0002g0063 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-8682delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54861503 | ||||||
| chr6:54861505 | C | G | 3 | a0002c0005t0013g0066 a0004c0014t0002g0062 a0004c0014t0002g0063 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-8682C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861505 | |||||||
| chr6:54861527 | G | A | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-8660G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861527 | |||||||
| chr6:54861529 | G | A | 50 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0049 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.-60-8658G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861529 | |||||||
| chr6:54861650 | A | G | 7 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-8537A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861650 | |||||||
| chr6:54861687 | C | T | 8 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(5): Show |
8 | HG00544.hp1 HG03491.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-60-8500C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861687 | |||||||
| chr6:54861745 | G | A | 118 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(115): Show |
119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-60-8442G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861745 | |||||||
| chr6:54861795 | C | T | 2 | a0001c0012t0008g0168 a0002c0026t0016g0254 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-60-8392C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861795 | |||||||
| chr6:54861869 | C | T | 1 | a0002c0023t0031g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-60-8318C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861869 | |||||||
| chr6:54862053 | A | G | 120 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0035g0022 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.-60-8134A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862053 | |||||||
| chr6:54862062 | T | C | 1 | a0003c0006t0007g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-60-8125T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862062 | |||||||
| chr6:54862071 | C | T | 90 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(87): Show |
90 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-60-8116C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862071 | |||||||
| chr6:54862110 | C | T | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-8077C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862110 | |||||||
| chr6:54862111 | G | A | 3 | a0001c0001t0001g0086 a0002c0005t0019g0240 a0002c0005t0019g0241 |
3 | HG02165.hp1 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-60-8076G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862111 | |||||||
| chr6:54862131 | T | C | 1 | a0002c0004t0003g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-60-8056T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862131 | |||||||
| chr6:54862181 | G | A | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-8006G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862181 | |||||||
| chr6:54862261 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-60-7926G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862261 | |||||||
| chr6:54862277 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-60-7910A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862277 | |||||||
| chr6:54862387 | C | T | 2 | a0001c0002t0002g0183 a0002c0028t0009g0188 |
2 | HG00323.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-60-7800C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862387 | |||||||
| chr6:54862430 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-60-7757A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862430 | |||||||
| chr6:54862635 | G | T | 8 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(5): Show |
8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-60-7552G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862635 | |||||||
| chr6:54862756 | T | C | 149 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(146): Show |
150 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-60-7431T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862756 | |||||||
| chr6:54862798 | C | A | 8 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(5): Show |
8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-60-7389C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862798 | |||||||
| chr6:54862864 | CA | C | 26 | a0001c0001t0001g0127 a0001c0012t0001g0005 a0001c0012t0002g0041 others(23): Show |
27 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-60-7318delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54862864 | ||||||
| chr6:54862869 | A | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
103 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-60-7318A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862869 | |||||||
| chr6:54862878 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-60-7309C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862878 | |||||||
| chr6:54862890 | GA | G | 11 | a0001c0001t0001g0126 a0001c0002t0002g0231 a0001c0008t0005g0012 others(8): Show |
11 | HG00544.hp1 HG01928.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.-60-7287delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54862890 | ||||||
| chr6:54862933 | A | T | 70 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(67): Show |
70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-60-7254A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862933 | |||||||
| chr6:54863017 | C | T | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-7170C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863017 | |||||||
| chr6:54863053 | C | T | 1 | a0001c0002t0002g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-60-7134C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863053 | |||||||
| chr6:54863206 | C | A | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-6981C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863206 | |||||||
| chr6:54863219 | G | T | 3 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0023t0031g0235 |
3 | HG02572.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-60-6968G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863219 | |||||||
| chr6:54863252 | A | C | 1 | a0001c0002t0002g0049 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-60-6935A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863252 | |||||||
| chr6:54863331 | G | T | 91 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(88): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-60-6856G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863331 | |||||||
| chr6:54863388 | A | C | 15 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(12): Show |
15 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-60-6799A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863388 | |||||||
| chr6:54863546 | C | CCAA | 16 | a0001c0002t0002g0256 a0002c0005t0013g0066 a0002c0005t0013g0201 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-60-6639_-60-6637d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54863546 | ||||||
| chr6:54863555 | G | GACTTTTG others(19): Show |
123 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(120): Show |
124 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-60-6628_-60-6627i others(28): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54863555 | ||||||
| chr6:54863991 | C | T | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-6196C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863991 | |||||||
| chr6:54864047 | T | G | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-6140T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864047 | |||||||
| chr6:54864156 | AT | A | 3 | a0002c0003t0003g0027 a0002c0003t0003g0037 a0002c0003t0003g0038 |
3 | HG01168.hp2 HG01169.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-60-6024delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54864156 | ||||||
| chr6:54864169 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
250 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.-60-6018A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864169 | |||||||
| chr6:54864443 | C | G | 1 | a0002c0003t0003g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-60-5744C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864443 | |||||||
| chr6:54864457 | C | T | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-5730C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864457 | |||||||
| chr6:54864570 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-60-5617T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864570 | |||||||
| chr6:54864587 | T | C | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-60-5600T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864587 | |||||||
| chr6:54864727 | G | A | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-60-5460G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864727 | |||||||
| chr6:54864793 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-60-5394A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864793 | |||||||
| chr6:54864813 | A | G | 1 | a0002c0003t0003g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-60-5374A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864813 | |||||||
| chr6:54864984 | T | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
246 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-60-5203T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864984 | |||||||
| chr6:54865001 | A | G | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-60-5186A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865001 | |||||||
| chr6:54865056 | A | C | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-5131A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865056 | |||||||
| chr6:54865151 | C | A | 91 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(88): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-60-5036C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865151 | |||||||
| chr6:54865196 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-60-4991A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865196 | |||||||
| chr6:54865363 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0132 |
2 | NA18953.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-60-4824C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865363 | |||||||
| chr6:54865379 | A | T | 1 | a0002c0004t0012g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-60-4808A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865379 | |||||||
| chr6:54865382 | T | C | 61 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-60-4805T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865382 | |||||||
| chr6:54865414 | A | C | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-4773A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865414 | |||||||
| chr6:54865546 | A | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(214): Show |
218 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.-60-4641A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865546 | |||||||
| chr6:54865585 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(123): Show |
127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-60-4602T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865585 | |||||||
| chr6:54865706 | C | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
246 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-60-4481C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865706 | |||||||
| chr6:54865781 | G | C | 1 | a0001c0002t0002g0057 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-60-4406G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865781 | |||||||
| chr6:54865914 | A | G | 2 | a0001c0012t0008g0168 a0002c0026t0016g0254 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-60-4273A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865914 | |||||||
| chr6:54865931 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-60-4256A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865931 | |||||||
| chr6:54865967 | CATA | C | 19 | a0001c0002t0002g0270 a0001c0002t0014g0266 a0001c0002t0014g0267 others(16): Show |
19 | HG01884.hp2 HG01891.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.-60-4188_-60-4186d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | ||||||
| chr6:54865967 | CATAATA | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(188): Show |
192 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-60-4191_-60-4186d others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | ||||||
| chr6:54865967 | CATAATAA others(2): Show |
C | 43 | a0001c0002t0002g0264 a0001c0012t0001g0005 a0001c0012t0002g0041 others(40): Show |
44 | HG00741.hp2 HG01069.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.-60-4194_-60-4186d others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | ||||||
| chr6:54865967 | CATAATAA others(8): Show |
C | 1 | a0001c0002t0002g0185 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-60-4200_-60-4186d others(17): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | ||||||
| chr6:54866013 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.-60-4174A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866013 | |||||||
| chr6:54866071 | C | G | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-4116C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866071 | |||||||
| chr6:54866153 | A | C | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-4034A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866153 | |||||||
| chr6:54866171 | A | G | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-4016A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866171 | |||||||
| chr6:54866201 | G | GT | 9 | a0001c0002t0001g0230 a0002c0003t0003g0021 a0002c0003t0003g0028 others(6): Show |
9 | HG01069.hp2 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-60-3974dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54866201 | ||||||
| chr6:54866201 | GT | G | 17 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(14): Show |
17 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-60-3974delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54866201 | ||||||
| chr6:54866218 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-60-3969C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866218 | |||||||
| chr6:54866435 | A | G | 1 | a0003c0006t0007g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-60-3752A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866435 | |||||||
| chr6:54866481 | C | A | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-3706C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866481 | |||||||
| chr6:54866521 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-60-3666G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866521 | |||||||
| chr6:54866734 | A | C | 4 | a0001c0002t0002g0183 a0001c0002t0002g0184 a0001c0002t0002g0191 others(1): Show |
4 | HG00323.hp1 HG02293.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-60-3453A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866734 | |||||||
| chr6:54866872 | A | C | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-3315A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866872 | |||||||
| chr6:54866899 | C | T | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-60-3288C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866899 | |||||||
| chr6:54866937 | A | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-60-3250A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866937 | |||||||
| chr6:54867070 | T | A | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-3117T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867070 | |||||||
| chr6:54867241 | A | G | 27 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0001c0012t0008g0168 others(24): Show |
28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-2946A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867241 | |||||||
| chr6:54867274 | T | C | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-2913T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867274 | |||||||
| chr6:54867333 | T | C | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-2854T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867333 | |||||||
| chr6:54867425 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-60-2762G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867425 | |||||||
| chr6:54867830 | A | G | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-60-2357A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867830 | |||||||
| chr6:54867832 | C | T | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-2355C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867832 | |||||||
| chr6:54868121 | G | A | 80 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(77): Show |
80 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-60-2066G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868121 | |||||||
| chr6:54868123 | G | A | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-2064G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868123 | |||||||
| chr6:54868167 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(123): Show |
127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-60-2020C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868167 | |||||||
| chr6:54868243 | A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-60-1944A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868243 | |||||||
| chr6:54868334 | T | G | 8 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-60-1853T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868334 | |||||||
| chr6:54868499 | G | A | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-1688G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868499 | |||||||
| chr6:54868568 | G | A | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-1619G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868568 | |||||||
| chr6:54868582 | C | G | 1 | a0002c0005t0003g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-60-1605C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868582 | |||||||
| chr6:54868677 | C | G | 16 | a0001c0002t0002g0256 a0002c0005t0013g0066 a0002c0005t0013g0201 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-60-1510C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868677 | |||||||
| chr6:54868789 | A | G | 1 | a0001c0002t0002g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-60-1398A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868789 | |||||||
| chr6:54869072 | G | A | 15 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(12): Show |
15 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-60-1115G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869072 | |||||||
| chr6:54869325 | C | T | 96 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(93): Show |
96 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-60-862C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869325 | |||||||
| chr6:54869388 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-60-799G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869388 | |||||||
| chr6:54869394 | G | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-60-793G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869394 | |||||||
| chr6:54869526 | T | A | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-661T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869526 | |||||||
| chr6:54869622 | C | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-565C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869622 | |||||||
| chr6:54869679 | A | G | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-60-508A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869679 | |||||||
| chr6:54869772 | G | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
257 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.-60-415G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869772 | |||||||
| chr6:54869782 | T | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-60-405T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869782 | |||||||
| chr6:54869804 | A | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(123): Show |
127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-60-383A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869804 | |||||||
| chr6:54869849 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-60-338A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869849 | |||||||
| chr6:54869987 | A | G | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-200A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869987 | |||||||
| chr6:54870053 | A | T | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-60-134A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54870053 | |||||||
| chr6:54870116 | T | G | 1 | a0001c0002t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-60-71T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54870116 | |||||||
| chr6:54870143 | C | A | 62 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-60-44C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54870143 | |||||||
| chr6:54870739 | G | C | 1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.444+49G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870739 | |||||||
| chr6:54870796 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.444+106G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870796 | |||||||
| chr6:54870808 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.444+118G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870808 | |||||||
| chr6:54870814 | A | G | 3 | a0001c0001t0010g0149 a0005c0015t0017g0020 a0005c0015t0017g0067 |
3 | HG02922.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.444+124A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870814 | |||||||
| chr6:54871170 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.444+480T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871170 | |||||||
| chr6:54871233 | GC | G | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+544delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871233 | |||||||
| chr6:54871334 | A | T | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+644A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871334 | |||||||
| chr6:54871389 | CA | C | 4 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+706delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871389 | ||||||
| chr6:54871555 | C | CAAT | 74 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(71): Show |
74 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.444+904_444+906dup others(3): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | ||||||
| chr6:54871555 | C | CAATAAT | 11 | a0001c0001t0001g0136 a0001c0001t0001g0143 a0001c0002t0002g0216 others(8): Show |
11 | HG00438.hp1 HG00639.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+901_444+906dup others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | ||||||
| chr6:54871555 | CAAT | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.444+904_444+906del others(3): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | ||||||
| chr6:54871555 | CAATAATA others(5): Show |
C | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.444+895_444+906del others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | ||||||
| chr6:54871634 | T | C | 1 | a0001c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.444+944T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871634 | |||||||
| chr6:54871648 | C | T | 1 | a0003c0006t0007g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+958C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871648 | |||||||
| chr6:54871729 | C | T | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+1039C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871729 | |||||||
| chr6:54871745 | C | CA | 100 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0070 others(97): Show |
100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.444+1081dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | ||||||
| chr6:54871745 | C | CAA | 35 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0159 others(32): Show |
36 | HG01069.hp2 HG01167.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.444+1080_444+1081d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | ||||||
| chr6:54871745 | C | CAAAAAAA others(3): Show |
1 | a0001c0008t0025g0019 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.444+1072_444+1081d others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | ||||||
| chr6:54871745 | CA | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0122 a0001c0001t0001g0144 others(8): Show |
11 | HG01074.hp2 HG01256.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+1081delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | ||||||
| chr6:54871801 | A | G | 8 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(5): Show |
8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+1111A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871801 | |||||||
| chr6:54871803 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.444+1113A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871803 | |||||||
| chr6:54871919 | C | G | 62 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.444+1229C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871919 | |||||||
| chr6:54871929 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.444+1239T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871929 | |||||||
| chr6:54872446 | G | C | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.444+1756G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872446 | |||||||
| chr6:54872633 | C | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
260 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.444+1943C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872633 | |||||||
| chr6:54872844 | C | T | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+2154C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872844 | |||||||
| chr6:54872992 | G | GT | 244 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
246 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.444+2307dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54872992 | ||||||
| chr6:54872998 | G | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
260 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.444+2308G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872998 | |||||||
| chr6:54873023 | T | A | 91 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(88): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.444+2333T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873023 | |||||||
| chr6:54873155 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.444+2465A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873155 | |||||||
| chr6:54873229 | T | C | 4 | a0001c0012t0008g0168 a0002c0026t0016g0254 a0003c0016t0007g0003 others(1): Show |
4 | HG02615.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+2539T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873229 | |||||||
| chr6:54873249 | T | C | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+2559T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873249 | |||||||
| chr6:54873267 | TTTG | T | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+2578_444+2580d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873267 | |||||||
| chr6:54873332 | G | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(262): Show |
267 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.444+2642G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873332 | |||||||
| chr6:54873348 | C | T | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+2658C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873348 | |||||||
| chr6:54873376 | G | T | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+2686G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873376 | |||||||
| chr6:54873448 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
98 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.444+2758A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873448 | |||||||
| chr6:54873533 | G | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+2843G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873533 | |||||||
| chr6:54873642 | CT | C | 4 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
4 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+2961delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54873642 | ||||||
| chr6:54873683 | G | C | 1 | a0004c0024t0008g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.444+2993G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873683 | |||||||
| chr6:54873690 | G | GT | 116 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(113): Show |
117 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.444+3015dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54873690 | ||||||
| chr6:54873690 | G | GTT | 8 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0143 others(5): Show |
8 | HG00438.hp1 HG00741.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+3014_444+3015d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54873690 | ||||||
| chr6:54873747 | T | C | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+3057T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873747 | |||||||
| chr6:54873794 | C | T | 6 | a0002c0005t0019g0240 a0002c0005t0019g0241 a0003c0007t0006g0236 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+3104C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873794 | |||||||
| chr6:54873910 | T | C | 1 | a0001c0002t0002g0029 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.444+3220T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873910 | |||||||
| chr6:54874061 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+3371A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874061 | |||||||
| chr6:54874159 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.444+3469C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874159 | |||||||
| chr6:54874275 | A | C | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+3585A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874275 | |||||||
| chr6:54874570 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.444+3880T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874570 | |||||||
| chr6:54874645 | G | A | 4 | a0001c0012t0008g0168 a0002c0026t0016g0254 a0003c0016t0007g0003 others(1): Show |
4 | HG02615.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+3955G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874645 | |||||||
| chr6:54874741 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.444+4051T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874741 | |||||||
| chr6:54874834 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0002g0142 |
3 | HG02698.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.444+4144C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874834 | |||||||
| chr6:54874982 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.444+4292G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874982 | |||||||
| chr6:54875099 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG00558.hp1 NA18960.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.444+4409C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875099 | |||||||
| chr6:54875273 | G | A | 4 | a0001c0012t0008g0168 a0002c0026t0016g0254 a0003c0016t0007g0003 others(1): Show |
4 | HG02615.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+4583G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875273 | |||||||
| chr6:54875363 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+4673A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875363 | |||||||
| chr6:54875418 | T | C | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+4728T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875418 | |||||||
| chr6:54875542 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.444+4852G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875542 | |||||||
| chr6:54875624 | A | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG00323.hp2 NA18963.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+4934A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875624 | |||||||
| chr6:54875639 | C | T | 4 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+4949C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875639 | |||||||
| chr6:54875640 | G | A | 12 | a0001c0001t0001g0148 a0001c0002t0002g0256 a0003c0007t0006g0169 others(9): Show |
12 | HG00544.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+4950G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875640 | |||||||
| chr6:54875663 | CGGAGGGG others(51): Show |
C | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.444+5021_444+5078d others(60): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54875663 | ||||||
| chr6:54875664 | G | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+4974G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875664 | |||||||
| chr6:54875672 | A | G | 1 | a0002c0004t0003g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.444+4982A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875672 | |||||||
| chr6:54875702 | G | A | 4 | a0001c0002t0002g0264 a0001c0002t0014g0266 a0001c0002t0014g0267 others(1): Show |
4 | NA18960.hp2 NA19010.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+5012G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875702 | |||||||
| chr6:54875706 | G | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+5016G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875706 | |||||||
| chr6:54875711 | GAAGAAGA others(51): Show |
G | 6 | a0001c0012t0001g0005 a0002c0003t0003g0027 a0002c0003t0003g0037 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+5026_444+5083d others(60): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54875711 | ||||||
| chr6:54875725 | G | GGGAAAGA others(2): Show |
114 | a0001c0002t0001g0157 a0001c0002t0001g0230 a0001c0002t0002g0029 others(111): Show |
115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.444+5037_444+5038i others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54875725 | ||||||
| chr6:54875743 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+5053A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875743 | |||||||
| chr6:54875856 | C | A | 2 | a0002c0010t0009g0068 a0002c0010t0009g0069 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.444+5166C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875856 | |||||||
| chr6:54875930 | T | C | 6 | a0002c0005t0019g0240 a0002c0005t0019g0241 a0003c0007t0006g0236 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+5240T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875930 | |||||||
| chr6:54876225 | C | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
97 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.444+5535C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876225 | |||||||
| chr6:54876278 | C | CAT | 18 | a0001c0001t0010g0065 a0001c0001t0010g0149 a0001c0002t0002g0033 others(15): Show |
18 | HG00423.hp2 HG01928.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+5629_444+5630d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | C | CATATATA others(1): Show |
4 | a0001c0001t0010g0058 a0001c0008t0005g0013 a0002c0004t0003g0154 others(1): Show |
4 | HG02809.hp2 NA18906.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+5623_444+5630d others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CAT | C | 22 | a0001c0002t0001g0230 a0001c0002t0002g0030 a0001c0002t0002g0035 others(19): Show |
22 | HG00558.hp2 HG00735.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.444+5629_444+5630d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATAT | C | 14 | a0001c0001t0010g0064 a0001c0001t0010g0200 a0001c0002t0002g0029 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.444+5627_444+5630d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATAT | C | 5 | a0001c0002t0002g0160 a0001c0002t0002g0187 a0001c0002t0002g0203 others(2): Show |
5 | HG01074.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+5625_444+5630d others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(1): Show |
C | 11 | a0001c0002t0002g0185 a0001c0002t0014g0268 a0001c0013t0005g0128 others(8): Show |
11 | HG00738.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+5623_444+5630d others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(3): Show |
C | 19 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(16): Show |
19 | HG00741.hp2 HG01167.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.444+5621_444+5630d others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(7): Show |
C | 4 | a0002c0005t0019g0240 a0002c0005t0019g0241 a0004c0014t0002g0062 others(1): Show |
4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+5617_444+5630d others(16): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(11): Show |
C | 2 | a0001c0012t0008g0168 a0002c0026t0016g0254 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+5613_444+5630d others(20): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(13): Show |
C | 5 | a0001c0002t0002g0198 a0001c0002t0002g0232 a0001c0002t0021g0158 others(2): Show |
5 | HG02165.hp2 NA18946.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+5611_444+5630d others(22): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(15): Show |
C | 2 | a0001c0002t0002g0190 a0001c0002t0002g0221 |
2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.444+5609_444+5630d others(24): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(17): Show |
C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
100 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.444+5607_444+5630d others(26): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(19): Show |
C | 1 | a0001c0002t0002g0229 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.444+5605_444+5630d others(28): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876278 | CATATATA others(21): Show |
C | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+5603_444+5630d others(30): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | ||||||
| chr6:54876327 | G | GC | 6 | a0002c0005t0019g0240 a0002c0005t0019g0241 a0003c0007t0006g0236 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+5637_444+5638i others(3): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876327 | |||||||
| chr6:54876327 | G | GT | 17 | a0001c0001t0001g0126 a0001c0001t0001g0143 a0001c0001t0001g0192 others(14): Show |
17 | HG00438.hp1 HG00544.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.444+5651dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876327 | ||||||
| chr6:54876451 | A | T | 8 | a0002c0005t0019g0240 a0002c0005t0019g0241 a0003c0007t0006g0236 others(5): Show |
8 | HG02615.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+5761A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876451 | |||||||
| chr6:54876522 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.444+5832G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876522 | |||||||
| chr6:54876540 | G | T | 1 | a0001c0001t0010g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+5850G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876540 | |||||||
| chr6:54876660 | G | T | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+5970G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876660 | |||||||
| chr6:54876664 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0112 |
2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.444+5974A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876664 | |||||||
| chr6:54876803 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.444+6113G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876803 | |||||||
| chr6:54876808 | G | C | 61 | a0001c0002t0001g0230 a0001c0002t0002g0029 a0001c0002t0002g0030 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.444+6118G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876808 | |||||||
| chr6:54876990 | G | C | 9 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(6): Show |
9 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+6300G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876990 | |||||||
| chr6:54877055 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+6365A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877055 | |||||||
| chr6:54877315 | AGG | A | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+6628_444+6629d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54877315 | ||||||
| chr6:54877381 | G | A | 49 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0070 others(46): Show |
49 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.444+6691G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877381 | |||||||
| chr6:54877446 | G | T | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.444+6756G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877446 | |||||||
| chr6:54877447 | C | T | 3 | a0002c0004t0003g0060 a0004c0018t0008g0059 a0004c0018t0008g0155 |
3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.444+6757C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877447 | |||||||
| chr6:54877470 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.444+6780G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877470 | |||||||
| chr6:54877512 | A | G | 1 | a0001c0002t0002g0215 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.444+6822A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877512 | |||||||
| chr6:54877518 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.444+6828C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877518 | |||||||
| chr6:54877591 | T | C | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+6901T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877591 | |||||||
| chr6:54877692 | T | C | 1 | a0001c0002t0002g0264 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.444+7002T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877692 | |||||||
| chr6:54877871 | C | A | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+7181C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877871 | |||||||
| chr6:54878323 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.444+7633C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878323 | |||||||
| chr6:54878449 | T | A | 2 | a0004c0018t0008g0059 a0004c0018t0008g0155 |
2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.444+7759T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878449 | |||||||
| chr6:54878707 | C | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+8017C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878707 | |||||||
| chr6:54878846 | GC | G | 61 | a0001c0002t0001g0230 a0001c0002t0002g0029 a0001c0002t0002g0030 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.444+8157delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878846 | |||||||
| chr6:54879015 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444+8325T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879015 | |||||||
| chr6:54879114 | G | A | 11 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(8): Show |
11 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+8424G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879114 | |||||||
| chr6:54879153 | A | T | 10 | a0001c0002t0002g0264 a0001c0002t0002g0270 a0001c0002t0014g0266 others(7): Show |
10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+8463A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879153 | |||||||
| chr6:54879200 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+8510G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879200 | |||||||
| chr6:54879221 | A | C | 1 | a0002c0004t0012g0176 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.444+8531A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879221 | |||||||
| chr6:54879251 | A | G | 1 | a0001c0002t0002g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+8561A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879251 | |||||||
| chr6:54879538 | A | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+8848A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879538 | |||||||
| chr6:54879563 | T | C | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+8873T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879563 | |||||||
| chr6:54879599 | C | T | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+8909C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879599 | |||||||
| chr6:54879652 | G | T | 13 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(10): Show |
13 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+8962G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879652 | |||||||
| chr6:54879682 | T | C | 1 | a0003c0006t0007g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+8992T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879682 | |||||||
| chr6:54879830 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.444+9140G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879830 | |||||||
| chr6:54879840 | T | A | 1 | a0004c0011t0008g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.444+9150T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879840 | |||||||
| chr6:54879866 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.444+9176T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879866 | |||||||
| chr6:54879902 | C | G | 4 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0002c0004t0003g0242 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+9212C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879902 | |||||||
| chr6:54879947 | A | C | 1 | a0002c0005t0018g0224 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.444+9257A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879947 | |||||||
| chr6:54879966 | A | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
260 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.444+9276A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879966 | |||||||
| chr6:54880039 | A | C | 1 | a0001c0002t0002g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.444+9349A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880039 | |||||||
| chr6:54880109 | C | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+9419C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880109 | |||||||
| chr6:54880128 | C | G | 1 | a0001c0002t0002g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.444+9438C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880128 | |||||||
| chr6:54880148 | G | A | 61 | a0001c0002t0001g0230 a0001c0002t0002g0029 a0001c0002t0002g0030 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.444+9458G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880148 | |||||||
| chr6:54880171 | G | T | 61 | a0001c0002t0001g0230 a0001c0002t0002g0029 a0001c0002t0002g0030 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.444+9481G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880171 | |||||||
| chr6:54880300 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+9610G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880300 | |||||||
| chr6:54880375 | A | G | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+9685A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880375 | |||||||
| chr6:54880399 | A | T | 1 | a0001c0002t0002g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.444+9709A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880399 | |||||||
| chr6:54880413 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.444+9723G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880413 | |||||||
| chr6:54880441 | C | CT | 48 | a0001c0001t0001g0126 a0001c0001t0001g0132 a0001c0001t0001g0146 others(45): Show |
49 | HG00642.hp1 HG01069.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.444+9772dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | ||||||
| chr6:54880441 | C | CTT | 5 | a0001c0001t0001g0070 a0001c0002t0002g0033 a0001c0002t0002g0220 others(2): Show |
5 | HG01243.hp1 HG02258.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+9771_444+9772d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | ||||||
| chr6:54880441 | C | CTTT | 62 | a0001c0002t0001g0230 a0001c0002t0002g0029 a0001c0002t0002g0030 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.444+9770_444+9772d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | ||||||
| chr6:54880441 | C | CTTTT | 6 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(3): Show |
6 | HG01109.hp2 HG02027.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+9769_444+9772d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | ||||||
| chr6:54880441 | CT | C | 5 | a0001c0001t0001g0083 a0001c0001t0001g0122 a0001c0001t0010g0065 others(2): Show |
5 | HG00323.hp2 HG01256.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+9772delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | ||||||
| chr6:54880519 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.444+9829A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880519 | |||||||
| chr6:54880692 | C | T | 1 | a0002c0010t0009g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.444+10002C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880692 | |||||||
| chr6:54880883 | TTAAA | T | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0239 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+10200_444+1020 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880883 | ||||||
| chr6:54880994 | T | A | 11 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(8): Show |
11 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+10304T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880994 | |||||||
| chr6:54881021 | T | G | 7 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+10331T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881021 | |||||||
| chr6:54881047 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.444+10357T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881047 | |||||||
| chr6:54881111 | A | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+10421A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881111 | |||||||
| chr6:54881142 | A | G | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+10452A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881142 | |||||||
| chr6:54881157 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.444+10467A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881157 | |||||||
| chr6:54881357 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
256 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.444+10667A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881357 | |||||||
| chr6:54881521 | T | C | 16 | a0001c0002t0002g0256 a0002c0005t0013g0066 a0002c0005t0013g0201 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+10831T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881521 | |||||||
| chr6:54881524 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.444+10834C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881524 | |||||||
| chr6:54881625 | A | G | 1 | a0002c0003t0003g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.444+10935A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881625 | |||||||
| chr6:54881862 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.444+11172C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881862 | |||||||
| chr6:54881927 | C | T | 1 | a0003c0006t0007g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+11237C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881927 | |||||||
| chr6:54882087 | A | ATG | 60 | a0001c0002t0001g0230 a0001c0002t0002g0029 a0001c0002t0002g0030 others(57): Show |
60 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.444+11398_444+1139 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54882087 | ||||||
| chr6:54882214 | C | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+11524C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882214 | |||||||
| chr6:54882339 | T | A | 2 | a0001c0001t0004g0077 a0001c0001t0004g0093 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.444+11649T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882339 | |||||||
| chr6:54882544 | G | T | 25 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+11854G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882544 | |||||||
| chr6:54882580 | T | C | 1 | a0002c0003t0003g0250 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+11890T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882580 | |||||||
| chr6:54882716 | C | T | 1 | a0004c0018t0008g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.444+12026C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882716 | |||||||
| chr6:54882721 | C | G | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444+12031C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882721 | |||||||
| chr6:54882803 | A | G | 26 | a0001c0012t0001g0005 a0001c0012t0002g0041 a0002c0003t0003g0001 others(23): Show |
27 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.444+12113A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882803 | |||||||
| chr6:54882894 | C | T | 6 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(3): Show |
6 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+12204C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882894 | |||||||
| chr6:54882910 | C | T | 8 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(5): Show |
8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+12220C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882910 | |||||||
| chr6:54882975 | G | A | 1 | a0001c0002t0001g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.444+12285G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882975 | |||||||
| chr6:54882992 | G | A | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+12302G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882992 | |||||||
| chr6:54883006 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.444+12316C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883006 | |||||||
| chr6:54883045 | C | T | 2 | a0003c0006t0007g0173 a0003c0006t0007g0174 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.444+12355C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883045 | |||||||
| chr6:54883144 | C | T | 2 | a0001c0012t0008g0168 a0002c0026t0016g0254 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+12454C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883144 | |||||||
| chr6:54883185 | C | T | 8 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(5): Show |
8 | HG01167.hp1 HG01361.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+12495C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883185 | |||||||
| chr6:54883196 | G | GC | 4 | a0001c0002t0015g0006 a0001c0013t0005g0128 a0001c0013t0005g0265 others(1): Show |
4 | HG04204.hp1 NA18965.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+12508dupC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883196 | ||||||
| chr6:54883204 | A | C | 45 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0071 others(42): Show |
46 | HG00323.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.444+12514A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883204 | |||||||
| chr6:54883223 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+12533G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883223 | |||||||
| chr6:54883225 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+12535G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883225 | |||||||
| chr6:54883253 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(256): Show |
261 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.444+12563T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883253 | |||||||
| chr6:54883320 | AT | A | 8 | a0002c0004t0033g0151 a0003c0006t0007g0165 a0003c0006t0007g0166 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+12639delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883320 | ||||||
| chr6:54883332 | G | GT | 18 | a0001c0001t0002g0125 a0001c0001t0010g0064 a0001c0002t0002g0159 others(15): Show |
18 | HG01243.hp2 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+12661dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883332 | ||||||
| chr6:54883332 | GT | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0025 others(167): Show |
172 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.444+12661delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883332 | ||||||
| chr6:54883332 | GTT | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0010g0149 others(15): Show |
18 | HG01175.hp2 HG01978.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+12660_444+1266 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883332 | ||||||
| chr6:54883420 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
137 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.444+12730C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883420 | |||||||
| chr6:54883421 | G | A | 55 | a0001c0001t0002g0125 a0001c0001t0002g0142 a0001c0002t0002g0033 others(52): Show |
55 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.444+12731G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883421 | |||||||
| chr6:54883459 | C | A | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+12769C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883459 | |||||||
| chr6:54883497 | G | T | 9 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(6): Show |
9 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+12807G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883497 | |||||||
| chr6:54883503 | T | G | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+12813T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883503 | |||||||
| chr6:54883524 | C | T | 1 | a0001c0002t0002g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.444+12834C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883524 | |||||||
| chr6:54883626 | G | A | 57 | a0001c0001t0002g0079 a0001c0001t0002g0125 a0001c0001t0002g0142 others(54): Show |
57 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.444+12936G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883626 | |||||||
| chr6:54883699 | A | T | 1 | a0001c0001t0001g0011 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.444+13009A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883699 | |||||||
| chr6:54883763 | G | GT | 6 | a0001c0001t0001g0141 a0001c0008t0005g0012 a0001c0008t0005g0014 others(3): Show |
6 | HG00544.hp1 NA18963.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+13073_444+1307 others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883763 | |||||||
| chr6:54883764 | G | GT | 20 | a0001c0002t0014g0266 a0002c0003t0003g0042 a0002c0004t0020g0026 others(17): Show |
20 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.444+13085dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883764 | ||||||
| chr6:54883764 | G | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
158 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.444+13074G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883764 | |||||||
| chr6:54883838 | C | G | 1 | a0002c0004t0003g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.444+13148C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883838 | |||||||
| chr6:54883883 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+13193C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883883 | |||||||
| chr6:54883902 | G | A | 2 | a0003c0006t0007g0245 a0003c0006t0007g0251 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.444+13212G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883902 | |||||||
| chr6:54883935 | C | T | 39 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(36): Show |
40 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+13245C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883935 | |||||||
| chr6:54884026 | A | G | 35 | a0001c0002t0002g0256 a0001c0002t0015g0006 a0001c0002t0015g0009 others(32): Show |
35 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.444+13336A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884026 | |||||||
| chr6:54884041 | C | T | 6 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+13351C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884041 | |||||||
| chr6:54884099 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
157 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.444+13409C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884099 | |||||||
| chr6:54884177 | C | CT | 4 | a0001c0001t0010g0064 a0001c0001t0010g0065 a0001c0001t0010g0200 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+13488dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884177 | ||||||
| chr6:54884217 | G | C | 1 | a0001c0001t0024g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.444+13527G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884217 | |||||||
| chr6:54884234 | G | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(208): Show |
213 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.444+13544G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884234 | |||||||
| chr6:54884257 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.444+13567G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884257 | |||||||
| chr6:54884259 | G | A | 1 | a0004c0011t0008g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.444+13569G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884259 | |||||||
| chr6:54884299 | T | TA | 7 | a0001c0002t0002g0180 a0002c0003t0003g0042 a0002c0009t0011g0163 others(4): Show |
7 | HG00741.hp2 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+13628dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | ||||||
| chr6:54884299 | T | TAA | 12 | a0001c0002t0015g0006 a0001c0013t0005g0128 a0001c0013t0005g0265 others(9): Show |
12 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+13627_444+1362 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | ||||||
| chr6:54884299 | T | TAAA | 11 | a0001c0002t0002g0256 a0001c0002t0015g0009 a0001c0008t0005g0018 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+13626_444+1362 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | ||||||
| chr6:54884299 | T | TAAAA | 129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.444+13625_444+1362 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | ||||||
| chr6:54884299 | T | TAAAAA | 36 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0001g0146 others(33): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.444+13624_444+1362 others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | ||||||
| chr6:54884318 | AG | A | 9 | a0001c0002t0002g0029 a0001c0002t0002g0031 a0001c0002t0002g0032 others(6): Show |
9 | HG00735.hp2 HG01167.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+13629delG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884318 | |||||||
| chr6:54884319 | G | A | 2 | a0001c0002t0002g0030 a0001c0002t0002g0046 |
2 | HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.444+13629G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884319 | |||||||
| chr6:54884350 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.444+13660C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884350 | |||||||
| chr6:54884351 | G | A | 11 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+13661G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884351 | |||||||
| chr6:54884443 | T | C | 1 | a0001c0002t0002g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.444+13753T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884443 | |||||||
| chr6:54884481 | C | CA | 8 | a0001c0001t0001g0092 a0001c0002t0001g0157 a0001c0002t0002g0198 others(5): Show |
8 | HG02258.hp1 HG02615.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+13809dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | ||||||
| chr6:54884481 | C | CAA | 16 | a0001c0001t0001g0126 a0002c0004t0003g0060 a0002c0004t0033g0151 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.444+13808_444+1380 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | ||||||
| chr6:54884481 | CA | C | 21 | a0001c0001t0010g0064 a0001c0001t0010g0065 a0001c0001t0010g0149 others(18): Show |
21 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.444+13809delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | ||||||
| chr6:54884481 | CAA | C | 14 | a0002c0003t0003g0042 a0002c0004t0020g0026 a0002c0004t0020g0052 others(11): Show |
14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+13808_444+1380 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | ||||||
| chr6:54884578 | A | G | 1 | a0002c0005t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.444+13888A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884578 | |||||||
| chr6:54884693 | A | T | 3 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0023t0031g0235 |
3 | HG02572.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.444+14003A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884693 | |||||||
| chr6:54884698 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+14008C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884698 | |||||||
| chr6:54884775 | A | AT | 32 | a0001c0002t0002g0256 a0001c0008t0005g0036 a0002c0004t0003g0060 others(29): Show |
32 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.444+14100dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884775 | ||||||
| chr6:54884775 | AT | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(129): Show |
134 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.444+14100delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884775 | ||||||
| chr6:54884817 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.444+14127T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884817 | |||||||
| chr6:54884858 | C | T | 1 | a0002c0010t0009g0007 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.444+14168C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884858 | |||||||
| chr6:54884865 | C | T | 3 | a0002c0005t0003g0017 a0005c0015t0017g0020 a0005c0015t0017g0067 |
3 | HG02258.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.444+14175C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884865 | |||||||
| chr6:54884889 | C | CT | 3 | a0001c0001t0002g0142 a0001c0002t0002g0185 a0001c0002t0002g0231 |
3 | HG00738.hp2 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.444+14199_444+1420 others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884889 | |||||||
| chr6:54884897 | C | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+14207C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884897 | |||||||
| chr6:54884973 | T | C | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+14283T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884973 | |||||||
| chr6:54885038 | C | T | 5 | a0001c0002t0015g0006 a0001c0002t0015g0009 a0001c0013t0005g0128 others(2): Show |
5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+14348C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885038 | |||||||
| chr6:54885051 | C | T | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.444+14361C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885051 | |||||||
| chr6:54885052 | G | A | 2 | a0002c0010t0009g0068 a0002c0010t0009g0069 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.444+14362G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885052 | |||||||
| chr6:54885348 | GTTTGA | G | 3 | a0002c0005t0003g0017 a0005c0015t0017g0020 a0005c0015t0017g0067 |
3 | HG02258.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.444+14662_444+1466 others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54885348 | ||||||
| chr6:54885395 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+14705A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885395 | |||||||
| chr6:54885402 | T | C | 1 | a0004c0024t0008g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.444+14712T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885402 | |||||||
| chr6:54885584 | A | G | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.444+14894A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885584 | |||||||
| chr6:54885690 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
136 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.444+15000C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885690 | |||||||
| chr6:54885733 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.444+15043C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885733 | |||||||
| chr6:54885737 | C | T | 8 | a0002c0004t0003g0060 a0002c0004t0033g0151 a0002c0010t0009g0007 others(5): Show |
8 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+15047C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885737 | |||||||
| chr6:54885738 | G | A | 9 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+15048G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885738 | |||||||
| chr6:54885929 | G | A | 1 | a0001c0002t0002g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.444+15239G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885929 | |||||||
| chr6:54885962 | TATA | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+15295_444+1529 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54885962 | ||||||
| chr6:54885985 | T | G | 1 | a0002c0005t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.444+15295T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885985 | |||||||
| chr6:54886303 | A | AT | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+15622dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886303 | ||||||
| chr6:54886303 | AT | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
90 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.444+15622delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886303 | ||||||
| chr6:54886383 | G | C | 3 | a0001c0002t0002g0186 a0001c0002t0002g0195 a0001c0002t0002g0229 |
3 | NA18964.hp2 NA18965.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.444+15693G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886383 | |||||||
| chr6:54886529 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.444+15839T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886529 | |||||||
| chr6:54886698 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.444+16008G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886698 | |||||||
| chr6:54886841 | A | G | 1 | a0001c0001t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.444+16151A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886841 | |||||||
| chr6:54886846 | AT | A | 5 | a0001c0002t0015g0006 a0001c0002t0015g0009 a0001c0013t0005g0128 others(2): Show |
5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+16162delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886846 | ||||||
| chr6:54886899 | T | G | 6 | a0002c0003t0003g0021 a0002c0003t0003g0028 a0002c0003t0003g0047 others(3): Show |
6 | HG01069.hp2 HG01243.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+16209T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886899 | |||||||
| chr6:54886904 | CTTA | C | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+16223_444+1622 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886904 | ||||||
| chr6:54886925 | A | G | 1 | a0002c0003t0003g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+16235A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886925 | |||||||
| chr6:54887023 | A | G | 12 | a0002c0003t0003g0042 a0002c0005t0013g0066 a0002c0005t0013g0201 others(9): Show |
12 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+16333A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887023 | |||||||
| chr6:54887182 | TA | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+16493delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887182 | |||||||
| chr6:54887391 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+16701C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887391 | |||||||
| chr6:54887442 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+16752A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887442 | |||||||
| chr6:54887715 | ATAAC | A | 13 | a0002c0004t0003g0060 a0002c0004t0033g0151 a0002c0005t0013g0066 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+17028_444+1703 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54887715 | ||||||
| chr6:54887783 | T | G | 30 | a0001c0002t0002g0256 a0001c0002t0015g0006 a0001c0002t0015g0009 others(27): Show |
30 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.444+17093T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887783 | |||||||
| chr6:54887845 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0132 |
2 | NA18953.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.444+17155T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887845 | |||||||
| chr6:54887895 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+17205C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887895 | |||||||
| chr6:54888009 | CT | C | 18 | a0001c0002t0002g0029 a0001c0002t0002g0034 a0001c0002t0002g0057 others(15): Show |
18 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+17326delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54888009 | ||||||
| chr6:54888018 | T | G | 4 | a0003c0007t0006g0236 a0003c0007t0006g0237 a0003c0007t0006g0238 others(1): Show |
4 | HG02615.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+17328T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888018 | |||||||
| chr6:54888187 | T | C | 1 | a0003c0006t0007g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.444+17497T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888187 | |||||||
| chr6:54888193 | A | G | 13 | a0002c0004t0003g0060 a0002c0004t0033g0151 a0002c0005t0013g0066 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+17503A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888193 | |||||||
| chr6:54888209 | T | C | 39 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(36): Show |
40 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+17519T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888209 | |||||||
| chr6:54888256 | A | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
157 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.444+17566A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888256 | |||||||
| chr6:54888274 | T | TTATTGTT others(30): Show |
9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+17595_444+1759 others(41): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54888274 | ||||||
| chr6:54888526 | T | C | 4 | a0001c0002t0002g0029 a0001c0002t0002g0034 a0001c0002t0002g0057 others(1): Show |
4 | NA18953.hp2 NA18977.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+17836T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888526 | |||||||
| chr6:54888542 | G | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
157 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.444+17852G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888542 | |||||||
| chr6:54888661 | C | A | 5 | a0001c0001t0004g0061 a0001c0001t0004g0095 a0001c0001t0004g0099 others(2): Show |
5 | HG01109.hp1 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+17971C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888661 | |||||||
| chr6:54888743 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(125): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+18053T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888743 | |||||||
| chr6:54888828 | A | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
136 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.444+18138A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888828 | |||||||
| chr6:54889056 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.444+18366T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889056 | |||||||
| chr6:54889087 | T | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+18397T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889087 | |||||||
| chr6:54889112 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00558.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.444+18422A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889112 | |||||||
| chr6:54889177 | G | A | 1 | a0002c0026t0016g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.444+18487G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889177 | |||||||
| chr6:54889442 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.444+18752A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889442 | |||||||
| chr6:54889447 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.444+18757C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889447 | |||||||
| chr6:54889467 | A | G | 13 | a0002c0004t0003g0060 a0002c0004t0033g0151 a0002c0005t0013g0066 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+18777A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889467 | |||||||
| chr6:54889468 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0131 others(4): Show |
7 | HG00735.hp1 HG00741.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+18778C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889468 | |||||||
| chr6:54889469 | G | A | 4 | a0003c0007t0006g0236 a0003c0007t0006g0237 a0003c0007t0006g0238 others(1): Show |
4 | HG02615.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+18779G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889469 | |||||||
| chr6:54889494 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+18804C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889494 | |||||||
| chr6:54890147 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.444+19457A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890147 | |||||||
| chr6:54890240 | AC | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+19552delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54890240 | ||||||
| chr6:54890349 | C | G | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+19659C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890349 | |||||||
| chr6:54890539 | C | T | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+19849C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890539 | |||||||
| chr6:54890541 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0071 others(6): Show |
9 | HG00438.hp1 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+19851A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890541 | |||||||
| chr6:54890590 | C | G | 9 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+19900C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890590 | |||||||
| chr6:54890953 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.444+20263A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890953 | |||||||
| chr6:54890954 | GA | G | 24 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(21): Show |
24 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.444+20275delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54890954 | ||||||
| chr6:54890992 | G | A | 25 | a0001c0002t0002g0256 a0002c0003t0003g0042 a0002c0004t0020g0026 others(22): Show |
25 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.444+20302G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890992 | |||||||
| chr6:54891073 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(157): Show |
162 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.444+20383G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891073 | |||||||
| chr6:54891156 | A | G | 1 | a0002c0003t0003g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.444+20466A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891156 | |||||||
| chr6:54891342 | C | CT | 132 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(129): Show |
133 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.444+20654dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54891342 | ||||||
| chr6:54891451 | A | G | 1 | a0001c0002t0002g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444+20761A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891451 | |||||||
| chr6:54891510 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(129): Show |
133 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.444+20820C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891510 | |||||||
| chr6:54891697 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(116): Show |
120 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.444+21007C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891697 | |||||||
| chr6:54891731 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
90 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.444+21041G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891731 | |||||||
| chr6:54891735 | A | G | 5 | a0001c0002t0015g0006 a0001c0002t0015g0009 a0001c0013t0005g0128 others(2): Show |
5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+21045A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891735 | |||||||
| chr6:54891853 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.444+21163C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891853 | |||||||
| chr6:54891949 | A | C | 5 | a0001c0002t0015g0006 a0001c0002t0015g0009 a0001c0013t0005g0128 others(2): Show |
5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+21259A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891949 | |||||||
| chr6:54892157 | A | G | 1 | a0001c0021t0005g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.444+21467A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892157 | |||||||
| chr6:54892159 | A | C | 40 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(37): Show |
41 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.444+21469A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892159 | |||||||
| chr6:54892268 | T | A | 1 | a0003c0007t0028g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.444+21578T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892268 | |||||||
| chr6:54892722 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
143 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.444+22032A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892722 | |||||||
| chr6:54892733 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+22043A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892733 | |||||||
| chr6:54892755 | A | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+22065A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892755 | |||||||
| chr6:54892828 | T | A | 4 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+22138T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892828 | |||||||
| chr6:54892838 | G | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+22148G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892838 | |||||||
| chr6:54892867 | A | C | 1 | a0001c0002t0002g0049 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.444+22177A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892867 | |||||||
| chr6:54892940 | G | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+22250G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892940 | |||||||
| chr6:54892993 | G | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(186): Show |
191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+22303G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892993 | |||||||
| chr6:54893271 | A | G | 11 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+22581A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893271 | |||||||
| chr6:54893352 | A | C | 2 | a0002c0003t0003g0252 a0002c0003t0026g0167 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.444+22662A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893352 | |||||||
| chr6:54893830 | G | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(186): Show |
191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+23140G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893830 | |||||||
| chr6:54893881 | A | G | 3 | a0002c0004t0003g0153 a0002c0004t0003g0154 a0003c0017t0006g0152 |
3 | HG02559.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.444+23191A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893881 | |||||||
| chr6:54893961 | A | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+23271A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893961 | |||||||
| chr6:54894216 | A | G | 57 | a0001c0012t0002g0041 a0001c0012t0008g0168 a0002c0003t0003g0001 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.444+23526A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894216 | |||||||
| chr6:54894428 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(186): Show |
191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+23738A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894428 | |||||||
| chr6:54894587 | G | A | 1 | a0001c0021t0005g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.444+23897G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894587 | |||||||
| chr6:54894595 | G | C | 1 | a0001c0002t0002g0032 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.444+23905G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894595 | |||||||
| chr6:54894685 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(113): Show |
117 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.444+23995A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894685 | |||||||
| chr6:54894697 | G | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(113): Show |
117 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.444+24007G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894697 | |||||||
| chr6:54894778 | CTT | C | 32 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(29): Show |
33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.444+24089_444+2409 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894778 | |||||||
| chr6:54895131 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(113): Show |
117 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.444+24441A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895131 | |||||||
| chr6:54895222 | A | G | 1 | a0002c0005t0019g0240 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.444+24532A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895222 | |||||||
| chr6:54895379 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.444+24689C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895379 | |||||||
| chr6:54895403 | A | G | 14 | a0002c0003t0003g0042 a0002c0004t0020g0026 a0002c0004t0020g0052 others(11): Show |
14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+24713A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895403 | |||||||
| chr6:54895469 | T | C | 73 | a0001c0012t0002g0041 a0001c0012t0008g0168 a0002c0003t0003g0001 others(70): Show |
74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.444+24779T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895469 | |||||||
| chr6:54895882 | C | CT | 6 | a0003c0016t0007g0003 a0003c0016t0027g0004 a0004c0011t0008g0257 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+25197dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54895882 | ||||||
| chr6:54895888 | G | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
114 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.444+25198G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895888 | |||||||
| chr6:54896000 | T | C | 57 | a0001c0012t0002g0041 a0001c0012t0008g0168 a0002c0003t0003g0001 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.444+25310T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896000 | |||||||
| chr6:54896125 | C | T | 2 | a0003c0016t0007g0003 a0003c0016t0027g0004 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+25435C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896125 | |||||||
| chr6:54896378 | A | G | 4 | a0003c0007t0006g0236 a0003c0007t0006g0237 a0003c0007t0006g0238 others(1): Show |
4 | HG02615.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+25688A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896378 | |||||||
| chr6:54896484 | C | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(186): Show |
191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+25794C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896484 | |||||||
| chr6:54896558 | C | A | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+25868C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896558 | |||||||
| chr6:54896609 | A | T | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444+25919A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896609 | |||||||
| chr6:54896724 | T | C | 9 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(6): Show |
9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+26034T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896724 | |||||||
| chr6:54896978 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0192 |
2 | NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.444+26288G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896978 | |||||||
| chr6:54897006 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+26316A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897006 | |||||||
| chr6:54897019 | C | T | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+26329C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897019 | |||||||
| chr6:54897038 | G | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+26348G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897038 | |||||||
| chr6:54897227 | T | TAAAA | 73 | a0001c0012t0002g0041 a0001c0012t0008g0168 a0002c0003t0003g0001 others(70): Show |
74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.444+26546_444+2654 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54897227 | ||||||
| chr6:54897413 | G | T | 1 | a0003c0006t0007g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.444+26723G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897413 | |||||||
| chr6:54897512 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.444+26822G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897512 | |||||||
| chr6:54897524 | A | C | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.444+26834A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897524 | |||||||
| chr6:54897642 | T | G | 1 | a0002c0003t0003g0250 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+26952T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897642 | |||||||
| chr6:54897681 | A | T | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444+26991A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897681 | |||||||
| chr6:54897827 | T | G | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.444+27137T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897827 | |||||||
| chr6:54897935 | G | A | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.444+27245G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897935 | |||||||
| chr6:54897992 | T | C | 2 | a0001c0008t0005g0013 a0001c0008t0005g0036 |
2 | NA18943.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.444+27302T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897992 | |||||||
| chr6:54898106 | G | T | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+27416G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898106 | |||||||
| chr6:54898166 | T | C | 21 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(18): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.444+27476T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898166 | |||||||
| chr6:54898220 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
140 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.444+27530G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898220 | |||||||
| chr6:54898375 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+27685T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898375 | |||||||
| chr6:54898603 | G | C | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-27768G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898603 | |||||||
| chr6:54898664 | C | T | 9 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-27707C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898664 | |||||||
| chr6:54898697 | C | G | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-27674C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898697 | |||||||
| chr6:54898697 | C | T | 11 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.445-27674C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898697 | |||||||
| chr6:54898720 | A | G | 5 | a0001c0001t0002g0142 a0001c0002t0002g0185 a0001c0002t0002g0196 others(2): Show |
5 | HG00738.hp2 HG01928.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-27651A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898720 | |||||||
| chr6:54898778 | G | A | 5 | a0002c0003t0003g0027 a0002c0003t0003g0037 a0002c0003t0003g0038 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-27593G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898778 | |||||||
| chr6:54898796 | G | A | 5 | a0001c0012t0008g0168 a0002c0005t0003g0017 a0002c0026t0016g0254 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-27575G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898796 | |||||||
| chr6:54898998 | C | T | 1 | a0001c0001t0023g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-27373C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898998 | |||||||
| chr6:54899148 | T | C | 5 | a0001c0012t0008g0168 a0002c0005t0003g0017 a0002c0026t0016g0254 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-27223T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899148 | |||||||
| chr6:54899223 | C | A | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-27148C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899223 | |||||||
| chr6:54899240 | G | A | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-27131G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899240 | |||||||
| chr6:54899250 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.445-27121A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899250 | |||||||
| chr6:54899385 | C | T | 1 | a0001c0002t0002g0032 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.445-26986C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899385 | |||||||
| chr6:54899509 | G | A | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-26862G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899509 | |||||||
| chr6:54899522 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
37 | HG00423.hp1 HG00558.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.445-26849A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899522 | |||||||
| chr6:54899559 | A | G | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-26812A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899559 | |||||||
| chr6:54899592 | C | G | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-26779C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899592 | |||||||
| chr6:54899627 | G | A | 1 | a0001c0002t0002g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.445-26744G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899627 | |||||||
| chr6:54899751 | G | A | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-26620G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899751 | |||||||
| chr6:54899768 | A | G | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-26603A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899768 | |||||||
| chr6:54899852 | T | C | 1 | a0001c0002t0002g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.445-26519T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899852 | |||||||
| chr6:54899862 | A | G | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-26509A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899862 | |||||||
| chr6:54900300 | C | T | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-26071C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900300 | |||||||
| chr6:54900657 | A | C | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-25714A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900657 | |||||||
| chr6:54900678 | G | A | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-25693G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900678 | |||||||
| chr6:54900685 | A | G | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-25686A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900685 | |||||||
| chr6:54900685 | A | T | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-25686A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900685 | |||||||
| chr6:54900711 | C | A | 14 | a0002c0003t0003g0042 a0002c0004t0020g0026 a0002c0004t0020g0052 others(11): Show |
14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.445-25660C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900711 | |||||||
| chr6:54900968 | T | C | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.445-25403T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900968 | |||||||
| chr6:54901087 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.445-25284G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901087 | |||||||
| chr6:54901245 | GTGTTCTT others(4): Show |
G | 1 | a0001c0001t0001g0146 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.445-25122_445-2511 others(15): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54901245 | ||||||
| chr6:54901357 | A | T | 1 | a0001c0002t0002g0184 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.445-25014A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901357 | |||||||
| chr6:54901420 | G | GATAA | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24948_445-2494 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54901420 | ||||||
| chr6:54901424 | G | C | 6 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-24947G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901424 | |||||||
| chr6:54901438 | A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-24933A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901438 | |||||||
| chr6:54901591 | C | T | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24780C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901591 | |||||||
| chr6:54901636 | A | G | 5 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-24735A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901636 | |||||||
| chr6:54901678 | G | T | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24693G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901678 | |||||||
| chr6:54901742 | A | C | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24629A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901742 | |||||||
| chr6:54901933 | G | A | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24438G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901933 | |||||||
| chr6:54902127 | T | G | 59 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-24244T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902127 | |||||||
| chr6:54902189 | G | A | 1 | a0004c0018t0008g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.445-24182G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902189 | |||||||
| chr6:54902293 | A | G | 1 | a0001c0002t0002g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445-24078A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902293 | |||||||
| chr6:54902316 | G | T | 1 | a0001c0001t0002g0094 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-24055G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902316 | |||||||
| chr6:54902577 | C | T | 1 | a0002c0003t0003g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.445-23794C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902577 | |||||||
| chr6:54902598 | G | GACATTTC others(3): Show |
1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-23767_445-2376 others(14): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54902598 | ||||||
| chr6:54902608 | T | C | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-23763T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902608 | |||||||
| chr6:54902664 | G | GGCTCCCC others(22): Show |
6 | a0003c0007t0006g0169 a0003c0007t0006g0239 a0003c0007t0006g0255 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-23705_445-2370 others(33): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54902664 | ||||||
| chr6:54902917 | T | G | 3 | a0003c0007t0006g0169 a0003c0007t0006g0255 a0003c0007t0006g0262 |
3 | HG02895.hp2 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.445-23454T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902917 | |||||||
| chr6:54903071 | T | G | 5 | a0001c0012t0008g0168 a0002c0005t0003g0017 a0002c0026t0016g0254 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-23300T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903071 | |||||||
| chr6:54903361 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.445-23010C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903361 | |||||||
| chr6:54903416 | C | T | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-22955C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903416 | |||||||
| chr6:54903515 | G | A | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-22856G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903515 | |||||||
| chr6:54903805 | T | A | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-22566T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903805 | |||||||
| chr6:54903841 | T | C | 21 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(18): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-22530T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903841 | |||||||
| chr6:54903958 | A | G | 2 | a0003c0006t0007g0245 a0003c0006t0007g0251 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.445-22413A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903958 | |||||||
| chr6:54903972 | A | T | 1 | a0001c0002t0002g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.445-22399A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903972 | |||||||
| chr6:54904085 | G | A | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-22286G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904085 | |||||||
| chr6:54904154 | T | G | 1 | a0001c0021t0005g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.445-22217T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904154 | |||||||
| chr6:54904363 | A | G | 1 | a0001c0002t0002g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.445-22008A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904363 | |||||||
| chr6:54904538 | G | C | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-21833G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904538 | |||||||
| chr6:54904555 | A | G | 59 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-21816A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904555 | |||||||
| chr6:54904602 | A | G | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-21769A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904602 | |||||||
| chr6:54904762 | C | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-21609C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904762 | |||||||
| chr6:54905072 | GGGCACCT others(34): Show |
G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0141 a0001c0001t0001g0193 others(1): Show |
4 | HG03831.hp2 NA19000.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-21297_445-2125 others(45): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54905072 | ||||||
| chr6:54905116 | GCA | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0141 a0001c0001t0001g0193 others(1): Show |
4 | HG03831.hp2 NA19000.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-21254_445-2125 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905116 | |||||||
| chr6:54905177 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-21194A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905177 | |||||||
| chr6:54905446 | T | C | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-20925T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905446 | |||||||
| chr6:54905531 | G | A | 39 | a0001c0002t0002g0202 a0001c0012t0002g0041 a0002c0003t0003g0001 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.445-20840G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905531 | |||||||
| chr6:54905544 | A | T | 1 | a0002c0003t0003g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445-20827A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905544 | |||||||
| chr6:54905577 | G | A | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-20794G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905577 | |||||||
| chr6:54905630 | A | T | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-20741A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905630 | |||||||
| chr6:54905786 | G | A | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-20585G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905786 | |||||||
| chr6:54905812 | CATA | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.445-20555_445-2055 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54905812 | ||||||
| chr6:54905871 | A | T | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-20500A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905871 | |||||||
| chr6:54906004 | T | A | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-20367T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906004 | |||||||
| chr6:54906053 | G | GA | 10 | a0001c0001t0001g0126 a0001c0001t0010g0058 a0001c0001t0010g0064 others(7): Show |
10 | HG02056.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-20303dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54906053 | ||||||
| chr6:54906053 | GA | G | 22 | a0001c0001t0023g0134 a0002c0003t0016g0253 a0002c0004t0020g0026 others(19): Show |
22 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.445-20303delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54906053 | ||||||
| chr6:54906053 | GAA | G | 39 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.445-20304_445-2030 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54906053 | ||||||
| chr6:54906071 | A | G | 7 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(4): Show |
7 | HG00544.hp1 NA18943.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-20300A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906071 | |||||||
| chr6:54906138 | A | G | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-20233A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906138 | |||||||
| chr6:54906221 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
140 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.445-20150G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906221 | |||||||
| chr6:54906232 | C | A | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-20139C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906232 | |||||||
| chr6:54906339 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(206): Show |
211 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.445-20032A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906339 | |||||||
| chr6:54906487 | C | T | 1 | a0001c0012t0002g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445-19884C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906487 | |||||||
| chr6:54906499 | C | A | 18 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(15): Show |
18 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.445-19872C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906499 | |||||||
| chr6:54906683 | C | T | 1 | a0002c0005t0003g0223 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.445-19688C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906683 | |||||||
| chr6:54906684 | G | A | 1 | a0002c0003t0026g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.445-19687G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906684 | |||||||
| chr6:54906716 | A | G | 2 | a0004c0014t0002g0062 a0004c0014t0002g0063 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-19655A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906716 | |||||||
| chr6:54906749 | A | G | 1 | a0002c0003t0003g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445-19622A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906749 | |||||||
| chr6:54906760 | A | G | 5 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-19611A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906760 | |||||||
| chr6:54906793 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-19578A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906793 | |||||||
| chr6:54906833 | A | C | 7 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(4): Show |
7 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-19538A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906833 | |||||||
| chr6:54906861 | A | T | 1 | a0002c0005t0013g0066 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.445-19510A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906861 | |||||||
| chr6:54907140 | C | T | 40 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0012t0002g0041 others(37): Show |
41 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.445-19231C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907140 | |||||||
| chr6:54907300 | G | A | 13 | a0001c0012t0002g0041 a0002c0003t0003g0027 a0002c0003t0003g0037 others(10): Show |
13 | HG00438.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.445-19071G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907300 | |||||||
| chr6:54907362 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.445-19009A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907362 | |||||||
| chr6:54907412 | G | GTA | 209 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(206): Show |
211 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.445-18958_445-1895 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907412 | ||||||
| chr6:54907484 | C | T | 2 | a0002c0003t0003g0250 a0002c0005t0003g0048 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.445-18887C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907484 | |||||||
| chr6:54907604 | T | TTTTTTTT others(298): Show |
10 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(7): Show |
10 | HG03195.hp1 HG03491.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-18764_445-1876 others(309): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907604 | ||||||
| chr6:54907604 | T | TTTTTTTT others(299): Show |
2 | a0001c0008t0005g0016 a0001c0013t0005g0269 |
2 | HG00544.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.445-18764_445-1876 others(310): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907604 | ||||||
| chr6:54907629 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.445-18742A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907629 | |||||||
| chr6:54907629 | AT | A | 57 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.445-18733delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907629 | ||||||
| chr6:54907638 | T | A | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-18733T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907638 | |||||||
| chr6:54907744 | G | A | 38 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-18627G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907744 | |||||||
| chr6:54907978 | A | C | 5 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-18393A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907978 | |||||||
| chr6:54908016 | G | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
139 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.445-18355G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908016 | |||||||
| chr6:54908131 | GAA | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.445-18223_445-1822 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54908131 | ||||||
| chr6:54908276 | T | C | 57 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.445-18095T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908276 | |||||||
| chr6:54908295 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-18076A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908295 | |||||||
| chr6:54908402 | G | C | 1 | a0002c0010t0009g0008 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.445-17969G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908402 | |||||||
| chr6:54908495 | ATTAG | A | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-17872_445-1786 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54908495 | ||||||
| chr6:54908841 | C | T | 32 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(29): Show |
33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-17530C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908841 | |||||||
| chr6:54908850 | A | G | 2 | a0002c0003t0016g0253 a0002c0004t0033g0151 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.445-17521A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908850 | |||||||
| chr6:54908956 | G | A | 5 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-17415G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908956 | |||||||
| chr6:54908988 | T | C | 21 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(18): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-17383T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908988 | |||||||
| chr6:54909019 | G | A | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-17352G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909019 | |||||||
| chr6:54909146 | G | GT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-17219dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54909146 | ||||||
| chr6:54909214 | G | A | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-17157G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909214 | |||||||
| chr6:54909373 | G | A | 1 | a0008c0020t0002g0080 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.445-16998G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909373 | |||||||
| chr6:54909412 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-16959G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909412 | |||||||
| chr6:54909414 | T | C | 5 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-16957T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909414 | |||||||
| chr6:54909449 | A | C | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-16922A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909449 | |||||||
| chr6:54909480 | G | T | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-16891G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909480 | |||||||
| chr6:54909624 | A | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-16747A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909624 | |||||||
| chr6:54909647 | G | A | 43 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-16724G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909647 | |||||||
| chr6:54909648 | C | A | 16 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-16723C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909648 | |||||||
| chr6:54909659 | G | A | 4 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0074 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-16712G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909659 | |||||||
| chr6:54909667 | C | T | 1 | a0002c0003t0003g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445-16704C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909667 | |||||||
| chr6:54909797 | C | T | 1 | a0004c0011t0008g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445-16574C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909797 | |||||||
| chr6:54910187 | G | T | 2 | a0003c0006t0007g0170 a0003c0006t0007g0171 |
2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.445-16184G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910187 | |||||||
| chr6:54910286 | T | G | 1 | a0001c0002t0002g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.445-16085T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910286 | |||||||
| chr6:54910388 | G | A | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-15983G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910388 | |||||||
| chr6:54910402 | T | TC | 5 | a0001c0001t0001g0025 a0001c0001t0001g0194 a0001c0001t0004g0077 others(2): Show |
5 | HG00741.hp1 HG01175.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-15966dupC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54910402 | ||||||
| chr6:54910587 | T | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-15784T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910587 | |||||||
| chr6:54910682 | T | G | 7 | a0002c0003t0003g0042 a0002c0009t0011g0163 a0002c0009t0011g0246 others(4): Show |
7 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-15689T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910682 | |||||||
| chr6:54910683 | C | G | 32 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(29): Show |
33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-15688C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910683 | |||||||
| chr6:54910775 | C | T | 6 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-15596C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910775 | |||||||
| chr6:54910877 | G | GT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
92 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.445-15486dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54910877 | ||||||
| chr6:54910882 | T | C | 5 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-15489T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910882 | |||||||
| chr6:54910897 | G | C | 6 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-15474G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910897 | |||||||
| chr6:54910996 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.445-15375C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910996 | |||||||
| chr6:54910997 | A | G | 2 | a0002c0003t0016g0253 a0002c0004t0033g0151 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.445-15374A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910997 | |||||||
| chr6:54911079 | C | A | 11 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-15292C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911079 | |||||||
| chr6:54911140 | C | CGT | 8 | a0001c0001t0002g0142 a0001c0001t0010g0200 a0001c0002t0002g0033 others(5): Show |
8 | HG01243.hp2 HG02257.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-15206_445-1520 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGT | 27 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(24): Show |
27 | HG00735.hp2 HG00741.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.445-15208_445-1520 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGTGT | 39 | a0001c0001t0001g0126 a0001c0001t0010g0064 a0001c0001t0010g0065 others(36): Show |
39 | HG00544.hp1 HG01175.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.445-15210_445-1520 others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGTGTG others(1): Show |
22 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0004g0099 others(19): Show |
22 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.445-15212_445-1520 others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGTGTG others(3): Show |
92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-15214_445-1520 others(14): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGTGTG others(5): Show |
6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0124 others(3): Show |
6 | HG02280.hp2 HG03669.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-15216_445-1520 others(16): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGTGTG others(7): Show |
11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp2 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-15218_445-1520 others(18): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | CGTGTGTG others(9): Show |
4 | a0002c0003t0003g0047 a0002c0005t0013g0066 a0005c0015t0017g0020 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-15220_445-1520 others(20): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | ||||||
| chr6:54911140 | C | T | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-15231C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911140 | |||||||
| chr6:54911190 | T | C | 1 | a0001c0001t0010g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-15181T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911190 | |||||||
| chr6:54911465 | T | C | 32 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(29): Show |
33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-14906T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911465 | |||||||
| chr6:54911484 | C | T | 2 | a0002c0003t0003g0001 a0002c0003t0003g0039 |
3 | HG02280.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445-14887C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911484 | |||||||
| chr6:54912097 | C | G | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-14274C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912097 | |||||||
| chr6:54912204 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.445-14167A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912204 | |||||||
| chr6:54912420 | CA | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0144 others(3): Show |
6 | HG00423.hp1 HG01074.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-13939delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54912420 | ||||||
| chr6:54912509 | A | C | 1 | a0001c0012t0001g0005 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.445-13862A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912509 | |||||||
| chr6:54912690 | C | T | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-13681C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912690 | |||||||
| chr6:54912875 | A | G | 1 | a0002c0003t0003g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445-13496A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912875 | |||||||
| chr6:54913035 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
137 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.445-13336G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913035 | |||||||
| chr6:54913143 | TA | T | 3 | a0001c0012t0008g0168 a0002c0005t0003g0017 a0002c0026t0016g0254 |
3 | HG02258.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-13224delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54913143 | ||||||
| chr6:54913303 | A | T | 1 | a0008c0020t0002g0080 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.445-13068A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913303 | |||||||
| chr6:54913334 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.445-13037G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913334 | |||||||
| chr6:54913513 | C | T | 1 | a0001c0001t0010g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.445-12858C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913513 | |||||||
| chr6:54913578 | T | C | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-12793T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913578 | |||||||
| chr6:54913630 | A | T | 1 | a0002c0003t0003g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.445-12741A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913630 | |||||||
| chr6:54913664 | C | A | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-12707C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913664 | |||||||
| chr6:54913805 | G | A | 18 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(15): Show |
18 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.445-12566G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913805 | |||||||
| chr6:54913854 | A | G | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-12517A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913854 | |||||||
| chr6:54913893 | CT | C | 20 | a0001c0001t0001g0122 a0001c0002t0002g0029 a0001c0002t0002g0030 others(17): Show |
20 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.445-12468delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54913893 | ||||||
| chr6:54913902 | T | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
126 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.445-12469T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913902 | |||||||
| chr6:54913902 | T | TA | 16 | a0002c0003t0003g0042 a0002c0005t0013g0066 a0002c0005t0013g0201 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-12469_445-1246 others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913902 | |||||||
| chr6:54913903 | T | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.445-12468T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913903 | |||||||
| chr6:54913918 | G | T | 1 | a0001c0013t0005g0265 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.445-12453G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913918 | |||||||
| chr6:54914047 | A | G | 18 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(15): Show |
18 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.445-12324A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914047 | |||||||
| chr6:54914056 | A | C | 11 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(8): Show |
11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-12315A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914056 | |||||||
| chr6:54914127 | C | T | 3 | a0001c0012t0008g0168 a0002c0005t0003g0017 a0002c0026t0016g0254 |
3 | HG02258.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-12244C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914127 | |||||||
| chr6:54914136 | G | A | 1 | a0002c0010t0009g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.445-12235G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914136 | |||||||
| chr6:54914721 | C | A | 59 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-11650C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914721 | |||||||
| chr6:54914838 | G | T | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-11533G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914838 | |||||||
| chr6:54914905 | C | A | 59 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-11466C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914905 | |||||||
| chr6:54914984 | T | C | 2 | a0005c0015t0017g0020 a0005c0015t0017g0067 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.445-11387T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914984 | |||||||
| chr6:54915365 | C | A | 1 | a0002c0003t0003g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.445-11006C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915365 | |||||||
| chr6:54915367 | G | A | 3 | a0004c0014t0002g0062 a0004c0014t0002g0063 a0004c0014t0002g0260 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.445-11004G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915367 | |||||||
| chr6:54915387 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.445-10984G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915387 | |||||||
| chr6:54915488 | C | G | 21 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(18): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-10883C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915488 | |||||||
| chr6:54915508 | TAGAAACT others(321): Show |
T | 59 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-10846_445-1051 others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915508 | ||||||
| chr6:54915581 | T | C | 1 | a0001c0021t0005g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.445-10790T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915581 | |||||||
| chr6:54915589 | G | T | 1 | a0004c0014t0002g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.445-10782G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915589 | |||||||
| chr6:54915667 | G | A | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-10704G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915667 | |||||||
| chr6:54915735 | A | G | 1 | a0001c0002t0001g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.445-10636A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915735 | |||||||
| chr6:54915755 | G | C | 9 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-10616G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915755 | |||||||
| chr6:54915812 | C | CA | 16 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0124 others(13): Show |
16 | HG00423.hp1 HG00735.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.445-10534dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | C | CAAAAA | 9 | a0001c0008t0025g0019 a0003c0007t0006g0169 a0003c0007t0006g0236 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-10538_445-1053 others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | C | CAAAAAA | 20 | a0001c0002t0002g0256 a0001c0008t0005g0012 a0001c0008t0005g0014 others(17): Show |
20 | HG00544.hp1 HG02109.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-10539_445-1053 others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | C | CAAAAAAA | 11 | a0001c0008t0005g0013 a0003c0006t0007g0165 a0003c0006t0007g0170 others(8): Show |
11 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.445-10540_445-1053 others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | C | CAAAAAAA others(3): Show |
3 | a0001c0002t0002g0034 a0001c0002t0002g0057 a0001c0002t0002g0135 |
3 | NA18953.hp2 NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.445-10543_445-1053 others(14): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0002g0029 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.445-10544_445-1053 others(15): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | C | CAAAAAAA others(5): Show |
5 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0032 others(2): Show |
5 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-10545_445-1053 others(16): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915812 | CA | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0122 others(13): Show |
16 | HG01069.hp1 HG01256.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-10534delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | ||||||
| chr6:54915845 | A | G | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-10526A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915845 | |||||||
| chr6:54915982 | C | G | 59 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-10389C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915982 | |||||||
| chr6:54916013 | A | G | 10 | a0001c0002t0002g0256 a0003c0007t0006g0169 a0003c0007t0006g0236 others(7): Show |
10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-10358A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916013 | |||||||
| chr6:54916036 | G | A | 5 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-10335G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916036 | |||||||
| chr6:54916217 | G | A | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-10154G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916217 | |||||||
| chr6:54916379 | AT | A | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-9983delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54916379 | ||||||
| chr6:54916558 | A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-9813A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916558 | |||||||
| chr6:54916590 | A | G | 44 | a0001c0012t0002g0041 a0002c0003t0003g0001 a0002c0003t0003g0021 others(41): Show |
45 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.445-9781A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916590 | |||||||
| chr6:54916743 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445-9628C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916743 | |||||||
| chr6:54916788 | T | C | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-9583T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916788 | |||||||
| chr6:54916802 | A | T | 1 | a0001c0002t0002g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.445-9569A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916802 | |||||||
| chr6:54916810 | C | T | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-9561C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916810 | |||||||
| chr6:54916940 | T | C | 34 | a0002c0003t0003g0042 a0002c0003t0016g0253 a0002c0004t0020g0026 others(31): Show |
34 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.445-9431T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916940 | |||||||
| chr6:54916964 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-9407G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916964 | |||||||
| chr6:54917476 | T | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-8895T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917476 | |||||||
| chr6:54917491 | A | G | 13 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-8880A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917491 | |||||||
| chr6:54917495 | A | C | 2 | a0005c0015t0017g0020 a0005c0015t0017g0067 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.445-8876A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917495 | |||||||
| chr6:54917846 | C | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18963.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.445-8525C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917846 | |||||||
| chr6:54917854 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-8517A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917854 | |||||||
| chr6:54917861 | C | G | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-8510C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917861 | |||||||
| chr6:54918095 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-8276A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918095 | |||||||
| chr6:54918416 | G | A | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-7955G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918416 | |||||||
| chr6:54918468 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-7903C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918468 | |||||||
| chr6:54918492 | A | G | 21 | a0002c0003t0016g0253 a0002c0004t0020g0026 a0002c0004t0020g0052 others(18): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-7879A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918492 | |||||||
| chr6:54918539 | G | A | 1 | a0004c0024t0008g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.445-7832G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918539 | |||||||
| chr6:54918572 | T | A | 19 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(16): Show |
19 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.445-7799T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918572 | |||||||
| chr6:54918613 | C | G | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-7758C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918613 | |||||||
| chr6:54918859 | C | G | 1 | a0001c0002t0002g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.445-7512C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918859 | |||||||
| chr6:54919141 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.445-7230A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919141 | |||||||
| chr6:54919254 | T | G | 1 | a0002c0004t0012g0218 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445-7117T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919254 | |||||||
| chr6:54919388 | C | A | 1 | a0001c0001t0002g0125 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.445-6983C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919388 | |||||||
| chr6:54919425 | T | C | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-6946T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919425 | |||||||
| chr6:54919579 | A | G | 4 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0173 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-6792A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919579 | |||||||
| chr6:54919654 | C | T | 1 | a0002c0003t0003g0055 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.445-6717C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919654 | |||||||
| chr6:54919733 | A | G | 1 | a0002c0003t0003g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-6638A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919733 | |||||||
| chr6:54919854 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.445-6517C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919854 | |||||||
| chr6:54919862 | T | C | 1 | a0002c0005t0013g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445-6509T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919862 | |||||||
| chr6:54920004 | T | C | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-6367T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920004 | |||||||
| chr6:54920039 | G | C | 2 | a0004c0018t0008g0059 a0004c0018t0008g0155 |
2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.445-6332G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920039 | |||||||
| chr6:54920238 | C | T | 1 | a0002c0004t0003g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445-6133C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920238 | |||||||
| chr6:54920749 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.445-5622A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920749 | |||||||
| chr6:54920827 | G | A | 16 | a0002c0003t0016g0253 a0002c0004t0020g0026 a0002c0004t0020g0052 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-5544G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920827 | |||||||
| chr6:54920983 | G | A | 60 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(57): Show |
61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.445-5388G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920983 | |||||||
| chr6:54921158 | C | T | 1 | a0002c0003t0016g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-5213C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921158 | |||||||
| chr6:54921242 | T | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0127 |
3 | HG01258.hp1 HG02055.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.445-5129T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921242 | |||||||
| chr6:54921244 | C | T | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-5127C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921244 | |||||||
| chr6:54921251 | A | G | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-5120A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921251 | |||||||
| chr6:54921358 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0194 |
2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5013G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921358 | |||||||
| chr6:54921362 | T | TACAGTCT others(3): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0194 |
2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5009_445-5008i others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921362 | |||||||
| chr6:54921363 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0194 |
2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5008C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921363 | |||||||
| chr6:54921365 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0194 |
2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5006G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921365 | |||||||
| chr6:54921492 | G | T | 1 | a0005c0015t0017g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445-4879G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921492 | |||||||
| chr6:54921579 | G | A | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-4792G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921579 | |||||||
| chr6:54921608 | A | G | 3 | a0004c0014t0002g0062 a0004c0014t0002g0063 a0004c0014t0002g0260 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.445-4763A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921608 | |||||||
| chr6:54921698 | A | G | 1 | a0001c0002t0002g0185 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.445-4673A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921698 | |||||||
| chr6:54921768 | T | C | 1 | a0001c0002t0002g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.445-4603T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921768 | |||||||
| chr6:54921797 | T | C | 2 | a0001c0012t0002g0041 a0008c0020t0002g0080 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.445-4574T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921797 | |||||||
| chr6:54921800 | A | G | 7 | a0003c0007t0006g0169 a0003c0007t0006g0239 a0003c0007t0006g0255 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-4571A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921800 | |||||||
| chr6:54921967 | C | T | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-4404C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921967 | |||||||
| chr6:54922060 | C | A | 16 | a0002c0003t0016g0253 a0002c0004t0020g0026 a0002c0004t0020g0052 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-4311C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922060 | |||||||
| chr6:54922161 | A | G | 13 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-4210A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922161 | |||||||
| chr6:54922465 | G | A | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-3906G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922465 | |||||||
| chr6:54922473 | AT | A | 13 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(10): Show |
13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-3896delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54922473 | ||||||
| chr6:54922717 | T | C | 1 | a0001c0001t0023g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-3654T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922717 | |||||||
| chr6:54922718 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.445-3653C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922718 | |||||||
| chr6:54922934 | C | T | 7 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0172 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-3437C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922934 | |||||||
| chr6:54922958 | A | G | 2 | a0004c0018t0008g0059 a0004c0018t0008g0155 |
2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.445-3413A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922958 | |||||||
| chr6:54923069 | G | A | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-3302G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923069 | |||||||
| chr6:54923090 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.445-3281G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923090 | |||||||
| chr6:54923095 | A | G | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-3276A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923095 | |||||||
| chr6:54923110 | C | T | 2 | a0002c0004t0003g0153 a0002c0004t0003g0154 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.445-3261C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923110 | |||||||
| chr6:54923115 | A | G | 1 | a0001c0008t0005g0015 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.445-3256A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923115 | |||||||
| chr6:54923254 | G | T | 1 | a0006c0027t0002g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-3117G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923254 | |||||||
| chr6:54923340 | T | A | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-3031T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923340 | |||||||
| chr6:54923435 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.445-2936C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923435 | |||||||
| chr6:54923442 | A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-2929A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923442 | |||||||
| chr6:54923454 | G | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.445-2917G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923454 | |||||||
| chr6:54923657 | G | A | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-2714G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923657 | |||||||
| chr6:54923790 | T | TA | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-2580dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923790 | ||||||
| chr6:54923818 | C | A | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-2553C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923818 | |||||||
| chr6:54923822 | T | C | 1 | a0001c0008t0005g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.445-2549T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923822 | |||||||
| chr6:54923866 | C | CT | 8 | a0001c0002t0015g0006 a0001c0002t0015g0009 a0004c0011t0008g0257 others(5): Show |
8 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-2492dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923866 | ||||||
| chr6:54923866 | CT | C | 13 | a0001c0001t0001g0073 a0001c0001t0001g0112 a0001c0001t0001g0130 others(10): Show |
13 | HG01243.hp2 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.445-2492delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923866 | ||||||
| chr6:54923927 | T | C | 20 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(17): Show |
20 | HG01175.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-2444T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923927 | |||||||
| chr6:54923979 | T | TA | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2390dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923979 | ||||||
| chr6:54924024 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-2347C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924024 | |||||||
| chr6:54924095 | G | T | 1 | a0001c0001t0004g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.445-2276G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924095 | |||||||
| chr6:54924129 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.445-2242C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924129 | |||||||
| chr6:54924188 | T | C | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-2183T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924188 | |||||||
| chr6:54924188 | TAC | T | 86 | a0001c0001t0010g0058 a0001c0001t0010g0064 a0001c0001t0010g0065 others(83): Show |
87 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.445-2156_445-2155d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54924188 | ||||||
| chr6:54924188 | TACAC | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
97 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.445-2158_445-2155d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54924188 | ||||||
| chr6:54924188 | TACACAC | T | 6 | a0002c0009t0011g0163 a0002c0009t0011g0246 a0002c0009t0011g0247 others(3): Show |
6 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-2160_445-2155d others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54924188 | ||||||
| chr6:54924211 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.445-2160A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924211 | |||||||
| chr6:54924226 | AC | A | 3 | a0001c0001t0010g0064 a0001c0001t0010g0065 a0001c0001t0010g0200 |
3 | HG02257.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.445-2144delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924226 | |||||||
| chr6:54924274 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-2097C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924274 | |||||||
| chr6:54924362 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-2009C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924362 | |||||||
| chr6:54924460 | T | C | 1 | a0002c0026t0016g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.445-1911T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924460 | |||||||
| chr6:54924511 | C | T | 3 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0039 |
4 | HG01243.hp1 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-1860C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924511 | |||||||
| chr6:54924722 | A | T | 1 | a0001c0002t0002g0227 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.445-1649A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924722 | |||||||
| chr6:54924956 | C | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0220 |
2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.445-1415C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924956 | |||||||
| chr6:54924998 | G | A | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-1373G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924998 | |||||||
| chr6:54925023 | A | G | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-1348A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925023 | |||||||
| chr6:54925122 | A | G | 1 | a0001c0002t0002g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.445-1249A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925122 | |||||||
| chr6:54925143 | A | G | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.445-1228A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925143 | |||||||
| chr6:54925186 | T | G | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-1185T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925186 | |||||||
| chr6:54925327 | A | T | 2 | a0003c0006t0007g0245 a0003c0006t0007g0251 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.445-1044A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925327 | |||||||
| chr6:54925685 | A | G | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-686A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925685 | |||||||
| chr6:54925688 | T | G | 84 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(81): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-683T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925688 | |||||||
| chr6:54925773 | CTG | C | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-595_445-594del others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54925773 | ||||||
| chr6:54925800 | G | T | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-571G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925800 | |||||||
| chr6:54925852 | A | G | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.445-519A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925852 | |||||||
| chr6:54925883 | A | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0137 a0001c0001t0001g0161 others(1): Show |
4 | HG01256.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-488A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925883 | |||||||
| chr6:54925930 | T | G | 1 | a0001c0002t0002g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.445-441T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925930 | |||||||
| chr6:54925959 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.445-412C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925959 | |||||||
| chr6:54925992 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-379A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925992 | |||||||
| chr6:54926002 | T | C | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.445-369T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54926002 | |||||||
| chr6:54926171 | G | T | 9 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-200G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54926171 | |||||||
| chr6:54926591 | T | C | 5 | a0001c0002t0002g0160 a0001c0002t0002g0162 a0001c0002t0002g0209 others(2): Show |
5 | HG00280.hp2 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+56T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926591 | |||||||
| chr6:54926606 | C | T | 13 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.609+71C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926606 | |||||||
| chr6:54926692 | T | C | 2 | a0005c0015t0017g0020 a0005c0015t0017g0067 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609+157T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926692 | |||||||
| chr6:54926783 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.609+248A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926783 | |||||||
| chr6:54926812 | T | C | 2 | a0001c0001t0004g0077 a0001c0001t0004g0093 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.609+277T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926812 | |||||||
| chr6:54926887 | A | G | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.609+352A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926887 | |||||||
| chr6:54926922 | A | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.609+387A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926922 | |||||||
| chr6:54926925 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
98 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.609+390G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926925 | |||||||
| chr6:54926975 | C | A | 6 | a0002c0010t0009g0007 a0002c0010t0009g0008 a0002c0010t0009g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+440C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926975 | |||||||
| chr6:54927040 | G | A | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.610-468G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927040 | |||||||
| chr6:54927079 | A | C | 1 | a0002c0010t0009g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.610-429A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927079 | |||||||
| chr6:54927163 | G | A | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.610-345G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927163 | |||||||
| chr6:54927201 | G | A | 60 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(57): Show |
61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.610-307G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927201 | |||||||
| chr6:54927252 | G | GT | 9 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(6): Show |
9 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-250dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 54927252 | ||||||
| chr6:54927263 | T | A | 2 | a0001c0001t0001g0193 a0001c0002t0001g0157 |
2 | NA19000.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.610-245T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927263 | |||||||
| chr6:54927328 | A | G | 2 | a0001c0002t0002g0160 a0001c0002t0002g0209 |
2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.610-180A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927328 | |||||||
| chr6:54927383 | GT | G | 33 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(30): Show |
34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.610-115delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 54927383 | ||||||
| chr6:54927410 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.610-98T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927410 | |||||||
| chr6:54927438 | A | G | 60 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(57): Show |
61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.610-70A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927438 | |||||||
| chr6:54927728 | T | TA | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0023 others(90): Show |
94 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.734+122dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54927728 | ||||||
| chr6:54927728 | T | TAA | 30 | a0001c0001t0001g0078 a0001c0001t0001g0121 a0001c0001t0001g0126 others(27): Show |
30 | HG01175.hp1 HG01175.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.734+121_734+122dup others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54927728 | ||||||
| chr6:54927728 | TA | T | 22 | a0001c0001t0001g0082 a0001c0001t0002g0125 a0001c0001t0002g0142 others(19): Show |
22 | HG00735.hp2 HG01069.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.734+122delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54927728 | ||||||
| chr6:54927794 | C | T | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+162C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54927794 | |||||||
| chr6:54928349 | G | A | 1 | a0001c0002t0002g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.734+717G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928349 | |||||||
| chr6:54928358 | G | C | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+726G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928358 | |||||||
| chr6:54928641 | C | A | 84 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(81): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.734+1009C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928641 | |||||||
| chr6:54928641 | C | T | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734+1009C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928641 | |||||||
| chr6:54928844 | G | T | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+1212G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928844 | |||||||
| chr6:54929059 | T | C | 84 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(81): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.734+1427T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929059 | |||||||
| chr6:54929062 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.734+1430C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929062 | |||||||
| chr6:54929635 | T | C | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+2003T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929635 | |||||||
| chr6:54929649 | G | A | 1 | a0002c0003t0003g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.734+2017G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929649 | |||||||
| chr6:54929724 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.734+2092A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929724 | |||||||
| chr6:54929743 | C | T | 1 | a0002c0005t0003g0223 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.734+2111C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929743 | |||||||
| chr6:54929860 | T | A | 1 | a0002c0026t0016g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.734+2228T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929860 | |||||||
| chr6:54930084 | A | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.734+2452A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930084 | |||||||
| chr6:54930222 | G | C | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.734+2590G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930222 | |||||||
| chr6:54930240 | G | A | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.734+2608G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930240 | |||||||
| chr6:54930249 | T | A | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+2617T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930249 | |||||||
| chr6:54930470 | T | C | 2 | a0002c0004t0003g0153 a0002c0004t0003g0154 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.734+2838T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930470 | |||||||
| chr6:54930563 | T | G | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+2931T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930563 | |||||||
| chr6:54930595 | C | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.734+2963C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930595 | |||||||
| chr6:54930786 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.734+3154G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930786 | |||||||
| chr6:54930817 | A | T | 2 | a0003c0006t0007g0245 a0003c0006t0007g0251 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.734+3185A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930817 | |||||||
| chr6:54930937 | C | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
214 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.734+3305C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930937 | |||||||
| chr6:54931004 | A | G | 45 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(42): Show |
46 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.734+3372A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931004 | |||||||
| chr6:54931111 | A | G | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.734+3479A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931111 | |||||||
| chr6:54931164 | T | C | 7 | a0002c0003t0003g0028 a0002c0003t0003g0043 a0002c0003t0003g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.734+3532T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931164 | |||||||
| chr6:54931484 | CTTATAAT others(2): Show |
C | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+3867_734+3875d others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54931484 | ||||||
| chr6:54931513 | T | A | 5 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+3881T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931513 | |||||||
| chr6:54931627 | C | T | 1 | a0001c0002t0002g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.734+3995C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931627 | |||||||
| chr6:54931803 | C | T | 5 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+4171C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931803 | |||||||
| chr6:54931847 | A | G | 1 | a0001c0008t0005g0018 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.734+4215A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931847 | |||||||
| chr6:54932007 | C | CT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(105): Show |
109 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.734+4395dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | ||||||
| chr6:54932007 | C | CTT | 25 | a0002c0003t0003g0027 a0002c0003t0003g0055 a0002c0004t0020g0052 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.734+4394_734+4395d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | ||||||
| chr6:54932007 | C | CTTT | 54 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0028 others(51): Show |
55 | HG00438.hp2 HG01168.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.734+4393_734+4395d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | ||||||
| chr6:54932007 | CT | C | 12 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(9): Show |
12 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.734+4395delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | ||||||
| chr6:54932032 | C | T | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+4400C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932032 | |||||||
| chr6:54932067 | A | G | 2 | a0005c0015t0017g0020 a0005c0015t0017g0067 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.734+4435A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932067 | |||||||
| chr6:54932086 | T | C | 84 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(81): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.734+4454T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932086 | |||||||
| chr6:54932165 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.734+4533C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932165 | |||||||
| chr6:54932294 | A | G | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+4662A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932294 | |||||||
| chr6:54932571 | A | T | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.734+4939A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932571 | |||||||
| chr6:54932676 | C | CTCAGATT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.734+5047_734+5048i others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932676 | ||||||
| chr6:54932815 | G | A | 1 | a0002c0003t0003g0040 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.734+5183G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932815 | |||||||
| chr6:54932831 | C | G | 2 | a0001c0002t0015g0006 a0001c0002t0015g0009 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.734+5199C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932831 | |||||||
| chr6:54933057 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734+5425C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933057 | |||||||
| chr6:54933142 | C | CT | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+5520dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54933142 | ||||||
| chr6:54933508 | T | C | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+5876T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933508 | |||||||
| chr6:54933561 | TG | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.734+5930delG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933561 | |||||||
| chr6:54933711 | T | C | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-5995T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933711 | |||||||
| chr6:54933735 | A | T | 11 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-5971A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933735 | |||||||
| chr6:54933919 | A | T | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-5787A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933919 | |||||||
| chr6:54933984 | A | G | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-5722A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933984 | |||||||
| chr6:54934049 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.735-5657G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934049 | |||||||
| chr6:54934058 | C | A | 1 | a0001c0002t0002g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.735-5648C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934058 | |||||||
| chr6:54934070 | G | T | 1 | a0002c0004t0003g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.735-5636G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934070 | |||||||
| chr6:54934089 | G | A | 44 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(41): Show |
45 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.735-5617G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934089 | |||||||
| chr6:54934112 | G | T | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-5594G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934112 | |||||||
| chr6:54934134 | C | T | 11 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(8): Show |
11 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-5572C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934134 | |||||||
| chr6:54934171 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.735-5535C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934171 | |||||||
| chr6:54934191 | G | A | 11 | a0003c0007t0006g0169 a0003c0007t0006g0236 a0003c0007t0006g0237 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-5515G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934191 | |||||||
| chr6:54934323 | T | C | 33 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(30): Show |
34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.735-5383T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934323 | |||||||
| chr6:54934355 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.735-5351A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934355 | |||||||
| chr6:54934467 | G | T | 13 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(10): Show |
13 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-5239G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934467 | |||||||
| chr6:54934538 | C | T | 3 | a0004c0014t0002g0062 a0004c0014t0002g0063 a0004c0014t0002g0260 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.735-5168C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934538 | |||||||
| chr6:54934683 | T | C | 2 | a0005c0015t0017g0020 a0005c0015t0017g0067 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.735-5023T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934683 | |||||||
| chr6:54934716 | G | C | 2 | a0003c0007t0006g0237 a0003c0007t0028g0234 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.735-4990G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934716 | |||||||
| chr6:54934810 | C | A | 2 | a0001c0001t0001g0010 a0001c0012t0001g0005 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.735-4896C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934810 | |||||||
| chr6:54935022 | T | A | 45 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(42): Show |
46 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.735-4684T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935022 | |||||||
| chr6:54935218 | G | A | 60 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(57): Show |
61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.735-4488G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935218 | |||||||
| chr6:54935346 | G | A | 1 | a0001c0002t0002g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.735-4360G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935346 | |||||||
| chr6:54935477 | A | G | 17 | a0001c0001t0002g0233 a0001c0002t0002g0049 a0001c0002t0002g0160 others(14): Show |
17 | HG00280.hp2 HG00639.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.735-4229A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935477 | |||||||
| chr6:54935521 | T | G | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-4185T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935521 | |||||||
| chr6:54935864 | T | C | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-3842T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935864 | |||||||
| chr6:54935934 | C | T | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-3772C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935934 | |||||||
| chr6:54935972 | T | C | 2 | a0005c0015t0017g0020 a0005c0015t0017g0067 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.735-3734T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935972 | |||||||
| chr6:54935991 | G | A | 1 | a0001c0002t0002g0213 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.735-3715G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935991 | |||||||
| chr6:54936015 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.735-3691T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936015 | |||||||
| chr6:54936016 | T | C | 13 | a0002c0003t0003g0027 a0002c0003t0003g0037 a0002c0003t0003g0038 others(10): Show |
13 | HG00438.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-3690T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936016 | |||||||
| chr6:54936076 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.735-3630A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936076 | |||||||
| chr6:54936209 | C | T | 1 | a0001c0002t0002g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.735-3497C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936209 | |||||||
| chr6:54936247 | G | C | 1 | a0002c0004t0033g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-3459G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936247 | |||||||
| chr6:54936284 | A | G | 1 | a0002c0004t0003g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.735-3422A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936284 | |||||||
| chr6:54936378 | T | C | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-3328T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936378 | |||||||
| chr6:54936551 | G | A | 84 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(81): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.735-3155G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936551 | |||||||
| chr6:54937079 | T | G | 12 | a0001c0008t0005g0012 a0001c0008t0005g0013 a0001c0008t0005g0014 others(9): Show |
12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-2627T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937079 | |||||||
| chr6:54937125 | A | G | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.735-2581A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937125 | |||||||
| chr6:54937130 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.735-2576G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937130 | |||||||
| chr6:54937246 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.735-2460C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937246 | |||||||
| chr6:54937307 | A | G | 3 | a0004c0014t0002g0062 a0004c0014t0002g0063 a0004c0014t0002g0260 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.735-2399A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937307 | |||||||
| chr6:54937323 | A | G | 1 | a0001c0012t0008g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.735-2383A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937323 | |||||||
| chr6:54937431 | A | G | 84 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(81): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.735-2275A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937431 | |||||||
| chr6:54937538 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.735-2168A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937538 | |||||||
| chr6:54937577 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
214 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.735-2129T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937577 | |||||||
| chr6:54937700 | G | A | 13 | a0002c0004t0020g0026 a0002c0004t0020g0052 a0002c0004t0030g0244 others(10): Show |
13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.735-2006G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937700 | |||||||
| chr6:54937711 | T | C | 11 | a0002c0005t0013g0066 a0002c0005t0013g0201 a0002c0005t0013g0225 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-1995T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937711 | |||||||
| chr6:54937795 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.735-1911A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937795 | |||||||
| chr6:54938004 | G | C | 24 | a0003c0006t0007g0165 a0003c0006t0007g0166 a0003c0006t0007g0170 others(21): Show |
24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-1702G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938004 | |||||||
| chr6:54938051 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0193 others(1): Show |
4 | HG03831.hp2 NA19000.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-1655C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938051 | |||||||
| chr6:54938182 | GT | G | 4 | a0002c0004t0012g0176 a0002c0004t0012g0179 a0002c0004t0012g0218 others(1): Show |
4 | HG00438.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-1522delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54938182 | ||||||
| chr6:54938208 | T | C | 60 | a0002c0003t0003g0001 a0002c0003t0003g0021 a0002c0003t0003g0027 others(57): Show |
61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.735-1498T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938208 | |||||||
| chr6:54938304 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.735-1402A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938304 | |||||||
| chr6:54938512 | C | T | 1 | a0001c0001t0010g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.735-1194C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938512 | |||||||
| chr6:54938524 | T | C | 7 | a0004c0011t0008g0257 a0004c0011t0008g0258 a0004c0011t0008g0259 others(4): Show |
7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-1182T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938524 | |||||||
| chr6:54938997 | T | C | 2 | a0001c0002t0002g0190 a0001c0002t0002g0221 |
2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.735-709T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938997 | |||||||
| chr6:54939260 | G | A | 13 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(10): Show |
13 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-446G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54939260 | |||||||
| chr6:54939644 | G | A | 2 | a0002c0005t0019g0240 a0002c0005t0019g0241 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.735-62G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54939644 | |||||||
| chr6:54939681 | A | G | 1 | a0002c0026t0016g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.735-25A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54939681 |